Resource

Id pipeline/hg38_clinical_annotation
Type annotation_pipeline
Version 0
Summary
Description
Labels

Pipeline Documentation

preamble

Summary Clinical Annotation Pipeline
Description This is a pipeline to annotate with Clinical resources
Input reference genome hg38/genomes/GRCh38-hg38

Annotators

worst_effect_MANE_1_5
Type:

Worst effect across all transcripts.

source: worst_effect
effect_details_MANE_1_5
Type:

Effect details for each affected transcript. Format: < transcript 1 >:<gene 1>:<effect 1>:<details 1>|...

source: effect_details
gene_effects_MANE_1_5
Type:

<gene_1>:<effect_1>|... A gene can be repeated.

source: gene_effects
Annotator type: effect_annotator

Annotator to identify the effect of the variant on protein coding.

More info

Resource
Type: genome
Summary:
HG38 reference genome
Resource
Type: gene_models
Summary:
MANE gene model version 1.5
normalized_allele
Type: (Internal)

Normalized allele.

source: normalized_allele
Annotator type: normalize_allele_annotator
No description
Resource
Type: genome
Summary:
HG38 reference genome
dbSNP_rs_number
Type:

dbSNP ID (i.e. rs number)

allele_aggregator: list [default]

HISTOGRAM
source: RS
Annotator type: allele_score_annotator

Annotator to use with scores that depend on allele like variant frequencies, etc.

Mode (mode parameter, applies to VCFAllele inputs only):

  • allele (default): exact chrom/pos/ref/alt match.
  • region: aggregates scores for all allele lines overlapping the annotatable's span.

Non-VCFAllele annotatables always use region aggregation.

More info

  • input_annotatable: normalized_allele
Resource
Type: allele_score
Summary:
dbSNP: A public database of genetic variations for research and clinical use.
gnomad_v4_exome_ALL_af
Type:

Alternate allele frequency

allele_aggregator: max [default]

HISTOGRAM
source: AF
Annotator type: allele_score_annotator

Annotator to use with scores that depend on allele like variant frequencies, etc.

Mode (mode parameter, applies to VCFAllele inputs only):

  • allele (default): exact chrom/pos/ref/alt match.
  • region: aggregates scores for all allele lines overlapping the annotatable's span.

Non-VCFAllele annotatables always use region aggregation.

More info

  • input_annotatable: normalized_allele
Resource
Type: allele_score
Summary:
gnomAD v4.1.0 exome variants (ALL)
gnomad_v4_genome_ALL_af
Type:

Alternate allele frequency

allele_aggregator: max [default]

HISTOGRAM
source: AF
Annotator type: allele_score_annotator

Annotator to use with scores that depend on allele like variant frequencies, etc.

Mode (mode parameter, applies to VCFAllele inputs only):

  • allele (default): exact chrom/pos/ref/alt match.
  • region: aggregates scores for all allele lines overlapping the annotatable's span.

Non-VCFAllele annotatables always use region aggregation.

More info

  • input_annotatable: normalized_allele
Resource
Type: allele_score
Summary:
gnomAD v4.1.0 genome variants (ALL)
clinical_significance
Type:

Aggregate germline classification for this single variant; multiple values are separated by a vertical bar

allele_aggregator: list [default]

HISTOGRAM
source: CLNSIG
clinical_disease_name
Type:

ClinVar's preferred disease name for the concept specified by disease identifiers in CLNDISDB

allele_aggregator: list [default]

HISTOGRAM
source: CLNDN
Annotator type: allele_score_annotator

Annotator to use with scores that depend on allele like variant frequencies, etc.

Mode (mode parameter, applies to VCFAllele inputs only):

  • allele (default): exact chrom/pos/ref/alt match.
  • region: aggregates scores for all allele lines overlapping the annotatable's span.

Non-VCFAllele annotatables always use region aggregation.

More info

  • input_annotatable: normalized_allele
Resource
Type: allele_score
Summary:
Measure used to assess the clinical significance of genetic variants
phyloP7way
Type:

The score is a number that reflects the conservation at a position.

position_aggregator: mean [default]

HISTOGRAM
source: phyloP7way
Annotator type: position_score_annotator

Annotator to use with genomic scores depending on genomic position like phastCons, phyloP, FitCons2, etc.

More info

Resource
Type: position_score
Summary:
Conservation score based on the multiple alignment of 7 species
AlphaMissense_pathogenicity
Type:

AlphaMissense Pathogenicity score is a deleteriousness score for missense variants

allele_aggregator: max [default]

HISTOGRAM
source: am_pathogenicity
AlphaMissense_class
Type:

AlphaMissense Class is a deleteriousness category for missense variants

allele_aggregator: list [default]

HISTOGRAM
source: am_class
Annotator type: allele_score_annotator

Annotator to use with scores that depend on allele like variant frequencies, etc.

Mode (mode parameter, applies to VCFAllele inputs only):

  • allele (default): exact chrom/pos/ref/alt match.
  • region: aggregates scores for all allele lines overlapping the annotatable's span.

Non-VCFAllele annotatables always use region aggregation.

More info

Resource
Type: allele_score
Summary:
Functional impact of mutations on protein function
hg19_annotatable
Type: (Internal)

The lifted over annotatable

source: liftover_annotatable
Annotator type: liftover_annotator

Annotator to lift over a variant from one reference genome to another.

More info

Resource
Type: liftover_chain
Summary:
Liftover Chain Hg38 to Hg19
Resource
Type: genome
Summary:
HG38 reference genome
Resource
Type: genome
Summary:
HG19 reference genome
MPC_score
Type:

Missense badness, PolyPhen-2, and Constraint. A deleteriousness prediction score for missense variants"

allele_aggregator: max [default]

HISTOGRAM
source: MPC
Annotator type: allele_score_annotator

Annotator to use with scores that depend on allele like variant frequencies, etc.

Mode (mode parameter, applies to VCFAllele inputs only):

  • allele (default): exact chrom/pos/ref/alt match.
  • region: aggregates scores for all allele lines overlapping the annotatable's span.

Non-VCFAllele annotatables always use region aggregation.

More info

  • input_annotatable: hg19_annotatable
Resource
Type: allele_score
Summary:
MPC (Missense badness, PolyPhen-2, and Constraint) is a composite score that predicts the impact of missense variants.
worst_effect_GENCODE_49
Type:

Worst effect across all transcripts.

source: worst_effect
effect_details_GENCODE_49
Type:

Effect details for each affected transcript. Format: < transcript 1 >:<gene 1>:<effect 1>:<details 1>|...

source: effect_details
gene_effects_GENCODE_49
Type:

<gene_1>:<effect_1>|... A gene can be repeated.

source: gene_effects
gene_list
Type: (Internal)

List of all genes

source: gene_list
Annotator type: effect_annotator

Annotator to identify the effect of the variant on protein coding.

More info

Resource
Type: genome
Summary:
HG38 reference genome
Resource
Type: gene_models
Summary:
GENCODE 49, basic gene annotation on the reference chromosomes, scaffolds, assembly patches and alternate loci (haplotypes)
pLI_rank_all
Type:

Gene rank after sorting by pLI intolerance score

gene_aggregator: dict [default]

HISTOGRAM
source: pLI_rank
pLI_rank_min
Type:

Gene rank after sorting by pLI intolerance score

gene_aggregator: min

HISTOGRAM
source: pLI_rank
Annotator type: gene_score_annotator
No description
Resource
Type: gene_score
Summary:
Probability of Loss-of-Function Intolerance
LOEUF_rank_all
Type:

Gene ranks after sorting by LOEUF scores

gene_aggregator: dict [default]

HISTOGRAM
source: LOEUF_rank
LOEUF_rank_min
Type:

Gene ranks after sorting by LOEUF scores

gene_aggregator: min

HISTOGRAM
source: LOEUF_rank
Annotator type: gene_score_annotator
No description
Resource
Type: gene_score
Summary:
Degree of intolerance to predicted Loss-of-Function (pLoF) variation

Files

Filename Size md5
genomic_resource.yaml 237.0 B c70460c66c53bdb446abcb4aad4f8404
hg38_clinical_annotation.yaml 2.81 KB 15b2a7e2542d8ea0be28b23e3c30b940
statistics/