Thank you Pierre, but I don't know which is the bed file for matching.
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Hi! I want to calculate a percent of coverage (or the read count witch cover it) of the exons that code for a gene. How can I do? Which is the pipeline? Is it possible to get this information starting from the BAM file?
I'll like to get a result that seems like this:
chr | start | end | reads | exons | gene_name | percent_of_coverage
I would like to use python tools
Thanks a lot
Andrea
Hello Andrea,
if you don't want to reinvent the wheel have a look at picard CollectHsMetrics with the PER_TARGET_COVERAGE parameter. The output looks pretty much as you like to have it.
fin swimmer
Thank you Pierre, but I don't know which is the bed file for matching.
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