Closed sunyounglee closed 6 years ago
I encounter the same problem while I used mpileup for samtoolsFile. Did you solve the problem?
I think I found the problem. This could be caused by differences between the chromosome names used in bam-window-files (eg. chr1, chr2……) and those used in annotation (with 1,2,3……) .
Hi, I'm trying to run the copycat. Following the code in manual (https://github.com/chrisamiller/copycat/, Usage), I have some problems when I running it.
I got the error msg below:
[1] "inferred bin size: 1000" [1] "calculating mapability content for read length 101 Sat Nov 19 15:48:54 2016" [1] "WARNING: annotations for read length of 101 don't exist" [1] "using annotations for read length of 100 which are close enough" Error in data.frame(..., check.names = FALSE) : arguments imply differing number of rows: 0, 2
My input files are: 1) bam window files for normal and tumor data generated from bam-window with -r (by read length) and -l (by library) options Chr Start GI10_N.101 chrM 1 222 chrM 1001 141 chrM 2001 144 chrM 3001 179 . . .
2) vcf files generated from samtools mpileup command
Here is the code I run:
runPairedSampleAnalysis(annotationDirectory="/Volumes/sylee1/SunYoung/Project/Clonality_Analysis/annotations/copycat.anno.hg19", outputDirectory="ccout", normal="/Volumes/sylee1/SunYoung/Project/Clonality_Analysis/GI10N_window", tumor="/Volumes/sylee1/SunYoung/Project/Clonality_Analysis/GI10T_window", inputType = "bins", maxCore=2, binSize=0, perLibrary=1, perReadLength=1, verbose=TRUE, minWidth=3, minMapability=0.6, dumpBins=TRUE, doGcCorrection=TRUE, samtoolsFileFormat="unknown", purity=1, normalSamtoolsFile="/Volumes/sylee1/SunYoung/Project/Clonality_Analysis/GI10N.raw.vcf", tumorSamtoolsFile="/Volumes/sylee1/SunYoung/Project/Clonality_Analysis/GI10T.raw.vcf”)
Do I something wrong? Could you let me know how I can run the copyCat?