(This article was originally published at Getting Genetics Done, and syndicated at StatsBlogs.)
Check out the app here:
http://apps.bioconnector.virginia.edu/covcalc/
And the source code on GitHub:
https://github.com/stephenturner/covcalc
Give it your read length, whether you're using single- or paired-end sequencing, select a genome or enter your own. Then, select whether you want to calculate (a) the number of reads you need to hit a target depth of coverage, or (b) the coverage depth you'll hit given a set number of sequencing reads. Once you make the selection, use the slider to adjust either the desired coverage or number of reads sequenced, and the output text below is automatically updated.
Shiny App: Coverage / Read Count Calculator
Please comment on the article here: Getting Genetics Done

