Thunder

From Genome Analysis Wiki
Revision as of 12:32, 15 October 2010 by Ylwtx (talk | contribs)
Jump to navigationJump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

This page documents how to perform variant calling from low-coverage sequencing data using glfmultiples and thunder.

Input Data

To get started, you will need glf files in the standard format glf format.

If you do not have glf files, you can generate them from bam files (bam format also specified in glf format bam format) using the following command line:

 samtools pileup -g -T 1 -f ref.fa my.bam > my.glf

How to Run

Important Filters