varscan(1)
variant detection in next-generation sequencing data
SYNOPSIS
varscan
[COMMAND] [OPTIONS]
DESCRIPTION
Variant detection in massively parallel sequencing. For one sample,
calls SNPs, indels, and consensus genotypes. For tumor-normal pairs,
further classifies each variant as Germline, Somatic, or LOH, and also
detects somatic copy number changes.
USAGE
COMMANDS:
- pileup2snp
-
Identify SNPs from a pileup file
- pileup2indel
-
Identify indels a pileup file
- pileup2cns
-
Call consensus and variants from a pileup file
- mpileup2snp
-
Identify SNPs from an mpileup file
- mpileup2indel
-
Identify indels an mpileup file
- mpileup2cns
-
Call consensus and variants from an mpileup file
- somatic
-
Call germline/somatic variants from tumor-normal pileups
- copynumber
-
Determine relative tumor copy number from tumor-normal pileups
- readcounts
-
Obtain read counts for a list of variants from a pileup file
- filter
-
Filter SNPs by coverage, frequency, p-value, etc.
- somaticFilter
-
Filter somatic variants for clusters/indels
- processSomatic
-
Isolate Germline/LOH/Somatic calls from output
- copyCaller
-
GC-adjust and process copy number changes from VarScan copynumber output
- compare
-
Compare two lists of positions/variants
- limit
-
Restrict pileup/snps/indels to ROI positions