Agreed. You can either include the "chr" prefix or not, but be consistent across all of your files.
Hi,
I am trying to use the command "genome music bmr calc-covg"
genome music bmr calc-covg --bam-list=/home/duttlab/Documents/pathbamfile --output-dir=/home/duttlab/Documents/musicoutput/ --reference-sequence=/home/duttlab/Documents/GRCh37/humang1kv37.fasta --roi-file /home/duttlab/Documents/cervical/755/BT755ROIfiltersorted_1based.roi
and I'm getting the following error:
"Skipping invalid ROI: chrX 44703299 44704123 DUSP21" (for all enteries)
my --bam-list= command contains the path to the bam files, both normal and tumor (tab delimited as specified)
"T755 /home/duttlab/Documents/cervical/755/B755_fixed_sorted_realn_DupRm_recal.bam /home/duttlab/Documents/cervical/755/T755_fixed_sorted_realn_DupRm_recal.bam"
the roi file is sorted and looks like
1 68934 70162 OR4F5
1 569269 569485 Unknown
1 6354680 6355176 ACOT7
1 8073164 8074463 ERRFI1
1 10381591 10382051 KIF1B
1 11155633 11156155 EXOSC10
1 12836961 12837859 PRAMEF12
1 12888195 12888841 PRAMEF11
1 12918652 12920660 PRAMEF2
1 13695437 13696255 PRAMEF18
the genome reference file is in .fasta format (build GRCh37)
Can somebody please help? Thanks in advance..
1 answer
IMHO, that's a prefix "chr" problem with the chromosome names. Check that your file contains "X" and not "chrX".
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