e0cb403b33
I used this walker for my mtdna analysis where the goal was to see how the chromosomes were represented by the sequences in the bam files. It is very useful as a first look at a new dataset if you want to have an idea of where most of the reads fall. It reports the number of reads in each contig, percetages, enrichment as well as the expected number of reads for each contig and enrichment given the size of your dataset. I will document it accordingly with the new documentation tool. It's in public, and I'm happy to support it. |
||
|---|---|---|
| public | ||
| settings | ||
| LICENSE | ||
| build.xml | ||
| ivy.xml | ||