copyCat
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a parallel R package for detecting copy-number alterations from short sequencing reads
Dear Chris, I am trying to run the copyCat in the paired mode as follows. ``` copyCat::runPairedSampleAnalysis( annotationDirectory="./annotations/", outputDirectory="./results/", normal="./data/10A_depth.regions.bed", tumor="./data/01A_depth.regions.bed", inputType="bins", readLength=100, maxCores=2, binSize=0, perLibrary=1, perReadLength=0, verbose=TRUE, minMapability=0.6, dumpBins=TRUE,...
When I use copyCat. I met this error: Using copyCat version 1.6.12 [1] "inferred bin size: 10000" [1] "calculating mapability content for read length 100 Fri Oct 22 14:59:56 2021"...
Can you please let me know how the normalization happens in specific to sex chromosomes and if it is any different from the autosomal chromosomes? Also, why are you taking...
I use samtools and bcftools call SNVs of tumor and normal bam, and got the VCF file for earch sample when running copyCat I meet this error [1] "inferred that...
If an incorrect annotation dir is given the `getAnnoDir()` function will first attempt to see if an ideal directory exist, if it doesn't it will look for additional directories `annodir/readlength.*`...
Hello, I have tried the copyCat and function runPairedSampleAnalysis() for CNV analysis but got below error. [1] "inferred bin size: 10000" [1] "Can't infer read length from window file headers"...