Description Usage Arguments Details Value References See Also
View source: R/06_variant.call.recalibration.R
A wrapper function to run GATK (BaseRecalibrator)
1 | gatk.baserecalibrator(fns.bam, output.dir, sample.name, ref.fa, ref.dbSNP, ref.gold_indels, unsafe=FALSE, run.cmd=TRUE, mc.cores=1)
|
fns.bam |
Path to input BAM files |
output.dir |
Output directory |
sample.name |
A character vector for the sample names |
ref.fa |
Reference fasta file |
ref.dbSNP |
Known SNP sites reference(VCF) |
ref.gold_indels |
Known sites to indel variant call format(VCF) |
unsafe |
A parameter value for -U ALLOW_N_CIGAR_READS in GATK. This parameter must be TRUE in RNA-seq data. |
run.cmd |
Whether to execute the command line (default=TRUE) |
mc.cores |
The number of cores to use. Must be at least one(default=1), and parallelization requires at least two cores. |
First pass of the base quality score recalibration. Generates a recalibration table based on various covariates. The default covariates are read group, reported quality score, machine cycle, and nucleotide context. This walker generates tables based on specified covariates via by-locus traversal operating only at sites that are in the known sites VCF.
GATK report file contained recalibration table by read group, quality scores and all the optional covariates. (e.g., .grp)
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
https://software.broadinstitute.org/gatk/
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