Hello everyone, I am new in usegalaxy, and I want to execute exomeDepth tool. I have files correct for this (BED file, two file.bam, one for control and the other for de treatment) in theoric. when I execute and finish the tool, I read this messenger
“Warning message:
In scan(file = file, what = what, sep = sep, quote = quote, dec = dec, :
number of items read is not a multiple of the number of columns
Error in countBamInGRanges.exomeDepth(bam.file = bam, index = index, granges = target, :
Some sequences in the target data frame cannot be found in the index of the BAM file
Calls: suppressMessages … withCallingHandlers → getBamCounts → countBamInGRanges.exomeDepth
Execution halted”
Can you check your inputs based on the assumptions found in the ExomeDepth information (below the Execute button)? There is a specific warning related to gender and some details regarding aggregate reference, minimum number of exons, etc.
Thank you for your reply. My inputs are one file of exon.bed, and two files, one control condition, and one file for the treatment. I don’t stand why I have errors. Do you use these tools? or could you show me some files? Or maybe you know of a tutorial for this tool?
look for test folder/files; this particular case of ExomeDepth was really obvious, because there are only one folder and it’s the test-data, but sometimes you have to search better;
Thank you for your reply. I want to say that I cloned that repository for the tools exomeDepth, but there is an error maybe in the input files or the database build for the genome of reference? I to use “Human Feb. 2009 GRCh37/hg19”
"Warning message:
In scan(file = file, what = what, sep = sep, quote = quote, dec = dec, :
number of items read is not a multiple of the number of columns
Warning messages:
1: In .Seqinfo.mergexy(x, y) :
Each of the 2 combined objects has sequence levels not in the other: