Update docs for 1.4.1 release
diff --git a/docs/dyn/genomics_v1beta2.annotations.html b/docs/dyn/genomics_v1beta2.annotations.html
index 4926994..4ab30d7 100644
--- a/docs/dyn/genomics_v1beta2.annotations.html
+++ b/docs/dyn/genomics_v1beta2.annotations.html
@@ -91,7 +91,7 @@
<p class="firstline">Updates an annotation. The update must respect all mutability restrictions and other invariants described on the annotation resource. Caller must have WRITE permission for the associated dataset. This method supports patch semantics.</p>
<p class="toc_element">
<code><a href="#search">search(body)</a></code></p>
-<p class="firstline">Searches for annotations which match the given criteria. Results are returned ordered by start position. Annotations which have matching start positions are ordered deterministically. Caller must have READ permission for the queried annotation sets.</p>
+<p class="firstline">Searches for annotations that match the given criteria. Results are returned ordered by start position. Annotations that have matching start positions are ordered deterministically. Caller must have READ permission for the queried annotation sets.</p>
<p class="toc_element">
<code><a href="#update">update(annotationId, body)</a></code></p>
<p class="firstline">Updates an annotation. The update must respect all mutability restrictions and other invariants described on the annotation resource. Caller must have WRITE permission for the associated dataset.</p>
@@ -109,18 +109,18 @@
{
"annotations": [ # The annotations to be created. At most 4096 can be specified in a single request.
- { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+ { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -129,7 +129,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -150,7 +150,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -158,10 +158,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -170,9 +170,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -195,18 +197,18 @@
"message": "A String", # Error message for this status, if any.
"code": 42, # The HTTP status code for this operation.
},
- "annotation": { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'. # The annotation, if any.
- "info": { # A map of additional data for this annotation.
+ "annotation": { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'. # The annotation, if any.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -215,7 +217,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -236,7 +238,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -244,10 +246,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -256,9 +258,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -280,18 +284,18 @@
body: object, The request body. (required)
The object takes the form of:
-{ # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+{ # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -300,7 +304,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -321,7 +325,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -329,10 +333,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -341,9 +345,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -357,18 +363,18 @@
Returns:
An object of the form:
- { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+ { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -377,7 +383,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -398,7 +404,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -406,10 +412,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -418,9 +424,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -450,18 +458,18 @@
Returns:
An object of the form:
- { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+ { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -470,7 +478,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -491,7 +499,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -499,10 +507,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -511,9 +519,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -533,18 +543,18 @@
body: object, The request body. (required)
The object takes the form of:
-{ # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+{ # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -553,7 +563,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -574,7 +584,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -582,10 +592,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -594,9 +604,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -610,18 +622,18 @@
Returns:
An object of the form:
- { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+ { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -630,7 +642,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -651,7 +663,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -659,10 +671,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -671,9 +683,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -686,7 +700,7 @@
<div class="method">
<code class="details" id="search">search(body)</code>
- <pre>Searches for annotations which match the given criteria. Results are returned ordered by start position. Annotations which have matching start positions are ordered deterministically. Caller must have READ permission for the queried annotation sets.
+ <pre>Searches for annotations that match the given criteria. Results are returned ordered by start position. Annotations that have matching start positions are ordered deterministically. Caller must have READ permission for the queried annotation sets.
Args:
body: object, The request body. (required)
@@ -694,7 +708,7 @@
{
"pageToken": "A String", # The continuation token, which is used to page through large result sets. To get the next page of results, set this parameter to the value of nextPageToken from the previous response.
- "range": { # A 0-based half-open genomic coordinate range for search requests. # If specified, this query matches only annotations which overlap this range.
+ "range": { # A 0-based half-open genomic coordinate range for search requests. # If specified, this query matches only annotations that overlap this range.
"start": "A String", # The start position of the range on the reference, 0-based inclusive. If specified, referenceId or referenceName must also be specified. Defaults to 0.
"referenceId": "A String", # The ID of the reference to query. At most one of referenceId and referenceName should be specified.
"end": "A String", # The end position of the range on the reference, 0-based exclusive. If specified, referenceId or referenceName must also be specified. If unset or 0, defaults to the length of the reference.
@@ -713,18 +727,18 @@
{
"nextPageToken": "A String", # The continuation token, which is used to page through large result sets. Provide this value in a subsequent request to return the next page of results. This field will be empty if there aren't any additional results.
"annotations": [ # The matching annotations.
- { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+ { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -733,7 +747,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -754,7 +768,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -762,10 +776,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -774,9 +788,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -798,18 +814,18 @@
body: object, The request body. (required)
The object takes the form of:
-{ # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+{ # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -818,7 +834,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -839,7 +855,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -847,10 +863,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -859,9 +875,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.
@@ -875,18 +893,18 @@
Returns:
An object of the form:
- { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample/individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
- "info": { # A map of additional data for this annotation.
+ { # An annotation describes a region of reference genome. The value of an annotation may be one of several canonical types, supplemented by arbitrary info tags. A variant annotation is represented by one or more of these canonical types. An annotation is not inherently associated with a specific sample or individual (though a client could choose to use annotations in this way). Example canonical annotation types are 'Gene' and 'Variant'.
+ "info": { # A string which maps to an array of values.
"a_key": [ # A string which maps to an array of values.
"A String",
],
},
"name": "A String", # The display name of this annotation.
"type": "A String", # The data type for this annotation. Must match the containing annotation set's type.
- "variant": { # A Variant annotation. # A variant annotation which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
+ "variant": { # A Variant annotation. # A variant annotation, which describes the effect of a variant on the genome, the coding sequence, and/or higher level consequences at the organism level e.g. pathogenicity. This field is only set for annotations of type VARIANT.
"type": "A String", # Type has been adapted from ClinVar's list of variant types.
"effect": "A String", # Effect of the variant on the coding sequence.
- "transcriptIds": [ # Google annotation ID of the transcripts affected by this variant. These should be provided when the variant is created.
+ "transcriptIds": [ # Google annotation IDs of the transcripts affected by this variant. These should be provided when the variant is created.
"A String",
],
"alternateBases": "A String", # The alternate allele for this variant. If multiple alternate alleles exist at this location, create a separate variant for each one, as they may represent distinct conditions.
@@ -895,7 +913,7 @@
{
"conceptId": "A String", # The MedGen concept id associated with this gene. Search for these IDs at http://www.ncbi.nlm.nih.gov/medgen/
"omimId": "A String", # The OMIM id for this condition. Search for these IDs at http://omim.org/
- "externalIds": [ # The set of external ids for this condition.
+ "externalIds": [ # The set of external IDs for this condition.
{
"sourceName": "A String", # The name of the source of this data.
"id": "A String", # The id used by the source of this data.
@@ -916,7 +934,7 @@
"reverseStrand": True or False, # Whether this range refers to the reverse strand, as opposed to the forward strand. Note that regardless of this field, the start/end position of the range always refer to the forward strand.
"referenceName": "A String", # The display name corresponding to the reference specified by referenceId, for example chr1, 1, or chrX.
},
- "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternate splicing pattern would be represented as separate transcript object. This field is only set for annotations of type TRANSCRIPT.
+ "transcript": { # A transcript represents the assertion that a particular region of the reference genome may be transcribed as RNA. # A transcript value represents the assertion that a particular region of the reference genome may be transcribed as RNA. An alternative splicing pattern would be represented as a separate transcript object. This field is only set for annotations of type TRANSCRIPT.
"codingSequence": { # The range of the coding sequence for this transcript, if any. To determine the exact ranges of coding sequence, intersect this range with those of the exons, if any. If there are any exons, the codingSequence must start and end within them.
#
# Note that in some cases, the reference genome will not exactly match the observed mRNA transcript e.g. due to variance in the source genome from reference. In these cases, exon.frame will not necessarily match the expected reference reading frame and coding exon reference bases cannot necessarily be concatenated to produce the original transcript mRNA.
@@ -924,10 +942,10 @@
"end": "A String", # The end of the coding sequence on this annotation's reference sequence, 0-based exclusive. Note that this position is relative to the reference start, and not the containing annotation start.
},
"geneId": "A String", # The annotation ID of the gene from which this transcript is transcribed.
- "exons": [ # The exons which compose this transcript. Exons are the pieces of the transcript which are spliced together, may be exported from a cell's nucleus, and may then be translated to protein. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
+ "exons": [ # The exons that compose this transcript. This field should be unset for genomes where transcript splicing does not occur, for example prokaryotes.
#
#
- # Introns are regions of the transcript which are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript which are not exons are introns.
+ # Introns are regions of the transcript that are not included in the spliced RNA product. Though not explicitly modeled here, intron ranges can be deduced; all regions of this transcript that are not exons are introns.
#
#
# Exonic sequences do not necessarily code for a translational product (amino acids). Only the regions of exons bounded by the codingSequence correspond to coding DNA sequence.
@@ -936,9 +954,11 @@
# Exons are ordered by start position and may not overlap.
{
"start": "A String", # The start position of the exon on this annotation's reference sequence, 0-based inclusive. Note that this is relative to the reference start, and not the containing annotation start.
- "frame": { # Wrapper message for int32. # The frame of this exon. Contains a value of 0, 1, or 2 which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
+ "frame": { # Wrapper message for `int32`. # The frame of this exon. Contains a value of 0, 1, or 2, which indicates the offset of the first coding base of the exon within the reading frame of the coding DNA sequence, if any. This field is dependent on the strandedness of this annotation (see Annotation.position.reverseStrand). For forward stranded annotations, this offset is relative to the exon.start. For reverse strand annotations, this offset is relative to the exon.end-1.
#
# Unset if this exon does not intersect the coding sequence. Upon creation of a transcript, the frame must be populated for all or none of the coding exons.
+ #
+ # The JSON representation for `Int32Value` is JSON number.
"value": 42, # The int32 value.
},
"end": "A String", # The end position of the exon on this annotation's reference sequence, 0-based exclusive. Note that this is relative to the reference start, and not the containing annotation start.