what about?
java -jar GenomeAnalysisTK.jar -T DepthOfCoverage -R [reference fasta] -I [bam file] -L [bed file]
which one is better?
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Hi everybody, I have bam files for RNAseq, and I know the coordinates for specific exons of interest. I would like to know if there is any way to overlap my bam files over those specific coordinates and get the coverage for those regions. I usually use bedtools coverage, but to compare between samples. I was wondering if I can create a bed files with my coordinates and do:
bedtools coverage -a my.bam -b mycoordintes.bed -s
will that work?
Many thanks!
you should use -abam
for eexample:
bedtools coverage -abam sorted.bam -b regions.bed.gz | grep ^all > mycoverage.tab
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