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small fixes to configs
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RaqManzano committed Mar 19, 2024
1 parent 8b919b3 commit f22561b
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Showing 4 changed files with 997 additions and 982 deletions.
8 changes: 4 additions & 4 deletions assets/samplesheet2.csv
Original file line number Diff line number Diff line change
@@ -1,4 +1,4 @@
patient,status,sample,lane,fastq_1,fastq_2,bam,bai,cram,crai,table,vcf
P01,0,SAMPLE_NORMAL,L01,/path/to/fastq/files/AEG588A1_S1_L001_R1_001.fastq.gz,/path/to/fastq/files/AEG588A1_S1_L001_R2_001.fastq.gz,,,,,,,
P01,1,SAMPLE_TUMOR,L01,/path/to/fastq/files/AEG588A4_S1_L001_R1_001.fastq.gz,/path/to/fastq/files/AEG588A4_S1_L001_R2_001.fastq.gz,,,,,,,
P01,2,SAMPLE_RNA,L01,/path/to/fastq/files/AEG588A6_S1_L001_R1_001.fastq.gz,/path/to/fastq/files/AEG588A6_S1_L001_R2_001.fastq.gz,,,,,,,
patient,status,sample,lane,fastq_1,fastq_2
P01,0,SAMPLE_NORMAL,L01,/path/to/fastq/files/AEG588A1_S1_L001_R1_001.fastq.gz,/path/to/fastq/files/AEG588A1_S1_L001_R2_001.fastq.gz
P01,1,SAMPLE_TUMOR,L01,/path/to/fastq/files/AEG588A4_S1_L001_R1_001.fastq.gz,/path/to/fastq/files/AEG588A4_S1_L001_R2_001.fastq.gz
P01,2,SAMPLE_RNA,L01,/path/to/fastq/files/AEG588A6_S1_L001_R1_001.fastq.gz,/path/to/fastq/files/AEG588A6_S1_L001_R2_001.fastq.gz
4 changes: 3 additions & 1 deletion conf/test_full.config
Original file line number Diff line number Diff line change
Expand Up @@ -19,7 +19,9 @@ params {
max_time = '8.h'

// Input data
input = "${projectDir}/tests/csv/3.0/fastq_triplet.csv"
input = "${projectDir}/tests/csv/3.0/fastq_triplet.csv"
outdir = 'rnadnavar_test_full'

// Small reference genome
wes = true
genome = 'GRCh38'
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32 changes: 24 additions & 8 deletions nextflow.config
Original file line number Diff line number Diff line change
Expand Up @@ -24,13 +24,19 @@ params {
save_reference = false
build_only_index = false // Only build the reference indexes
download_cache = false // Do not download annotation cache
fasta_fai = null
dict = null



// Sequence read information
read_length = 76 // Required for STAR to build index and align reads TODO: automate
wes = false // Set to true, if data is exome/targeted sequencing data. Used to use correct models in various variant callers

// Alignment
bwa = null
bwamem2 = null
star_index = null
aligner = 'bwa-mem' // Only STAR is currently supported.
star_twopass = true
star_ignore_sjdbgtf = false // Ignore GTF file while creating index or alignment by STAR
Expand All @@ -48,6 +54,7 @@ params {
save_mapped = false // Mapped BAMs not saved
hisat2_index = null
dragmap = null
gff = null


// Modify fastqs (trim/split) with FASTP
Expand All @@ -61,12 +68,18 @@ params {
save_trimmed = false
save_split_fastqs = false

exon_bed = null

// Variant calling
no_intervals = false
intervals = null
nucleotides_per_second = 200000 // Default interval size
germline_resource = null
germline_resource_tbi = null
dbsnp = null
dbsnp_tbi = null
known_indels = null
known_indels_tbi = null
known_snps = null
known_snps_tbi = null
pon = null
Expand All @@ -85,8 +98,8 @@ params {
ignore_soft_clipped_bases = true

// Variant annotation
tools = null // No default Variant_Calling or Annotation tools
genesplicer = null // genesplicer disabled within VEP
tools = null // No default Variant_Calling or Annotation tools
genesplicer = null // genesplicer disabled within VEP
dbnsfp = null // No dbnsfp processed file
dbnsfp_consequence = null // No default consequence for dbnsfp plugin
dbnsfp_fields = "rs_dbSNP,HGVSc_VEP,HGVSp_VEP,1000Gp3_EAS_AF,1000Gp3_AMR_AF,LRT_score,GERP++_RS,gnomAD_exomes_AF" // Default fields for dbnsfp plugin
Expand All @@ -95,14 +108,17 @@ params {
spliceai_indel_tbi = null // No spliceai_indel file index
spliceai_snv = null // No spliceai_snv file
spliceai_snv_tbi = null // No spliceai_snv file index
vep_custom_args= "--no_progress --offline --shift_hgvs 1 --check_existing --tsl --domains --total_length --allele_number --no_escape --xref_refseq --failed 1 --flag_pick_allele --pick_order canonical,tsl,biotype,rank,ccds,length --format vcf --biotype --force_overwrite --sift p --polyphen p --variant_class --regulatory --allele_number --af_gnomad --af_gnomadg --gene_phenotype --hgvs --hgvsg --max_af"
vep_custom_args = "--no_progress --offline --shift_hgvs 1 --check_existing --tsl --domains --total_length --allele_number --no_escape --xref_refseq --failed 1 --flag_pick_allele --pick_order canonical,tsl,biotype,rank,ccds,length --format vcf --biotype --force_overwrite --sift p --polyphen p --variant_class --regulatory --allele_number --af_gnomad --af_gnomadg --gene_phenotype --hgvs --hgvsg --max_af"
vep_cache = null // No directory for VEP cache
vep_include_fasta = false // Don't use fasta file for annotation with VEP
vep_dbnsfp = null
vep_loftee = null
vep_spliceai = null
vep_spliceregion = null
vep_out_format = 'vcf'
vep_dbnsfp = null
vep_loftee = null
vep_spliceai = null
vep_spliceregion = null
vep_out_format = 'vcf'
vep_cache_version = '110'
vep_species = 'homo_sapiens'
vep_genome = null
outdir_cache = null // No default outdir cache

//filtering
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