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update test_full
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ramprasadn committed Jan 15, 2025
1 parent 4e71e74 commit 120481c
Showing 1 changed file with 36 additions and 21 deletions.
57 changes: 36 additions & 21 deletions conf/test_full.config
Original file line number Diff line number Diff line change
Expand Up @@ -14,28 +14,43 @@ params {
config_profile_name = 'Full test profile'
config_profile_description = 'Full test dataset to check pipeline function'

// Input data for full size test
input = params.pipelines_testdata_base_path + 'raredisease/testdata/samplesheet_full.csv'
intervals_wgs = params.pipelines_testdata_base_path + 'raredisease/reference/test_full/genome.interval_list'
intervals_y = params.pipelines_testdata_base_path + 'raredisease/reference/test_full/genomeY.interval_list'
target_bed = params.pipelines_testdata_base_path + 'raredisease/reference/test_full/target.bed'
variant_catalog = params.pipelines_testdata_base_path + 'raredisease/reference/test_full/variant_catalog_hg38.json'

// Genome references
genome = 'GRCh38'
// reference params
igenomes_ignore = true
mito_name = 'MT'

// Skip annotation
skip_mt_annotation = true
skip_snv_annotation = true
skip_sv_annotation = true
}
// analysis params
skip_germlinecnvcaller = true
skip_peddy = true

process {
withName: 'MARKDUPLICATES' {
memory = { check_max( 90.GB * task.attempt, 'memory' ) }
}
withName: 'DEEPVARIANT' {
cpus = 24
memory = { check_max( 90.GB * task.attempt, 'memory' ) }
}
// Input data
input = params.pipelines_testdata_base_path + 'raredisease/testdata/samplesheet_trio.csv'

// Genome references
fasta = params.pipelines_testdata_base_path + 'raredisease/reference/reference.fasta'
fai = params.pipelines_testdata_base_path + 'raredisease/reference/reference.fasta.fai'
genome = 'GRCh37'
gnomad_af = params.pipelines_testdata_base_path + 'raredisease/reference/gnomad_reformated.tab.gz'
intervals_wgs = params.pipelines_testdata_base_path + 'raredisease/reference/target_wgs.interval_list'
intervals_y = params.pipelines_testdata_base_path + 'raredisease/reference/targetY.interval_list'
known_dbsnp = params.pipelines_testdata_base_path + 'raredisease/reference/dbsnp_-138-.vcf.gz'
ml_model = 'https://s3.amazonaws.com/sentieon-release/other/SentieonDNAscopeModel1.1.model'
mobile_element_references = params.pipelines_testdata_base_path + 'raredisease/reference/mobile_element_references.tsv'
mobile_element_svdb_annotations = params.pipelines_testdata_base_path + 'raredisease/reference/svdb_querydb_files.csv'
reduced_penetrance = params.pipelines_testdata_base_path + 'raredisease/reference/reduced_penetrance.tsv'
score_config_mt = params.pipelines_testdata_base_path + 'raredisease/reference/rank_model_snv.ini'
score_config_snv = params.pipelines_testdata_base_path + 'raredisease/reference/rank_model_snv.ini'
score_config_sv = params.pipelines_testdata_base_path + 'raredisease/reference/rank_model_sv.ini'
svdb_query_dbs = params.pipelines_testdata_base_path + 'raredisease/reference/svdb_querydb_files.csv'
target_bed = params.pipelines_testdata_base_path + 'raredisease/reference/target.bed'
variant_catalog = params.pipelines_testdata_base_path + 'raredisease/reference/variant_catalog.json'
vcfanno_lua = params.pipelines_testdata_base_path + 'raredisease/reference/vcfanno_functions.lua'
vcfanno_resources = params.pipelines_testdata_base_path + 'raredisease/reference/vcfanno_resources.txt'
vcfanno_toml = params.pipelines_testdata_base_path + 'raredisease/reference/vcfanno_config.toml'
variant_consequences_snv = params.pipelines_testdata_base_path + 'raredisease/reference/variant_consequences_v2.txt'
variant_consequences_sv = params.pipelines_testdata_base_path + 'raredisease/reference/variant_consequences_v2.txt'
vep_cache = params.pipelines_testdata_base_path + 'raredisease/reference/vep_cache_and_plugins.tar.gz'
vep_filters = params.pipelines_testdata_base_path + 'raredisease/reference/hgnc.txt'
vep_cache_version = 107
vep_plugin_files = params.pipelines_testdata_base_path + 'raredisease/reference/vep_files.csv'
}

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