212
edits
Changes
From Genome Analysis Wiki
Jump to navigationJump to searchCreated page with '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 bam files in…'
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 bam files in the standard format [http://samtools.sourceforge.net/SAM1.pdf bam format].
== How to Run ==
== Important Filters ==
== Input Data ==
To get started, you will need bam files in the standard format [http://samtools.sourceforge.net/SAM1.pdf bam format].
== How to Run ==
== Important Filters ==
