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parameters_template.txt
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parameters_template.txt
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; NAME OF FILE CONTAINING LOGS
LOGFILE=<PREFIX>_logfile_fastgbs.log
; FLOWCELL INFORMATION
FLOWCELL=<FLOWCEL>
; LANES INFORMATION
CD5NCANXX_LANES=<LANE>
; SEQUENCING TECHNOLOGY: ILLUMINA IONTORRENT
TECHNOLOGY=ILLUMINA
; SEQUENCE TYPE: SE (Single End) or PE (Paired Ends)
SEQTYPE=SE
; NAME OF THE REFERENCE GENOME FILES --> PREFIX YOU CHOSE + .fa
REFGEN=<PREFIX>.fa
; SEQUENCE USED FOR ADAPTOR RECOGNITION (THE COMPLETE ADAPTOR SEQUENCE IS
; AGATCGGAAGAGCGGG)
ADAPFOR=AGATCGGAAG
; IF PAIRED END READS, ADD ADAPTER SEQUENCE IN REVERSE SEQUENCE (R2)
ADAPREV=AGATCGGAAG
; MINIMUM READ LENGTH TO KEEP
READLEN=50
; NUMBER OF PARALLEL PROCESS FOR BWA
BWAPAR=4
; NUMBER OF THREAD FOR EACH BWA PROCESS
BWATHR=4
; MAXIMUM NUMBER OF CORES THAT COULD BE ALLOWED BY YOUR COMPUTER FOR THIS ANALYSIS
; SHOULD BE EQUAL TO: BWAPAR X BWATHR
NBCOR=16
; OPTION TO MOVE SAMPLES WITH LESS THAN 10% THE AVERAGE NUMBER OF SAMPLES IN THE POOL: YES or NO
MVSAMPLES=YES
; OPTION TO SAVE DISK SPACE; DELETE INTERMEDIARY FILES: NO or YES
DELFILES=YES
DELLIST=*.fq *.sam *.temp.bam *.unknown.barcodes
; NAME OF FILE CONTAINING LIST OF S1.BAM FILE FOR PLATYPUS ANALYSIS
BAMLIST=List_bam
; VARIANT CALING FROM A DATABASE: None or vcf file
SOURCE=None
; FOR PLATYPUS: Minimum number of supporting reads required before a
; variant candidate will be considered (equivalent to minDP in vcftools)
MINREADS=2
; PLATYPUS LOGFILE
LOGPLAT=<PREFIX>_FastGBS_platypus_log.txt
;PROPORTION OF MISSING DATA (0 to 1 (no missing data)) AND MAF (minimum allele frequency, 0 to 1)
MAX-MISSING=0.2
MAF=0.01
; PLATYPUS OUTPUT VCF FILE
OUTPLAT=<PREFIX>_FastGBS_platypus