Description Usage Arguments Format Examples
Snvs and indels calling of paired tumor-normal wgs using manta
1 |
normal |
Normal bam file. |
tumor |
Tumour bam file. |
ref |
Reference genome. |
outPath |
Path where the output of the analysis will be saved. |
cores |
Number of cores to use. |
outName |
Name for the output file for the paired tumor normal analysis |
indelCandidates |
For the somatic workflow, the best-practice recommendation is to run the Manta SV and indel caller on the same set of samples first, then supply Manta's candidate indels as input to Strelka |
An object of class character
of length 1.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 | ## Not run:
normal <- 'raw/sample1_BL.bam'
tumor <- 'raw/sample1_TI.bam'
ref <- '/imppc/labs/lplab/share/marc/refgen/hg38/hg38.fa'
outPath <- 'dir/vcf'
cores <- 4
outName <- 'sample1'
indelCandidates <- /results/variants/candidateSmallIndels.vcf.gz
strelka2(normal = normal,
tumor = tumor,
ref = ref,
outPath = outPath,
cores = cores,
outName = outName)
## End(Not run)
|
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