gravatar for nalexandre

4 hours ago by

Hello,

I used samtools depth to get a textfile of coverage across my genome for ~600 samples. In order to inform coverage cutoffs in the next step I'd like to make a summary/histogram of some sort that summarizes coverage for all of these genomes together.

For example, eventually I'd like to say, filter out reads below x coverage and above y coverage. This would be based on the distribution of coverage for all samples to filter out likely duplicates etc.

Any help is appreciated!



Source link