- This product has not had a release in over 1 year and may no longer be maintained.
Post Alignment SNV Tools
With single nucleotide variations (SNVs) being identified in ever increasing numbers with next generation sequencing data, we are often interested in a breakdown of the effect of the mutations, and if a particular change is somatic or germline. We are also interested in high quality true positive mutations, which are increasingly important considering their use in clinical decisions. PASsiT is a suite of tools developed to help us address these needs in our high-throughput sequencing and analysis environment.
See poster presented at RECOMB 2011 for more details:
Released Apr 01, 2011
First release of PASsiT tools set.
More about this release…
- Get PASsiT for Linux
- PASsiT 1.0
- If you are using Plone 3.2 or higher, you probably want to install this product with buildout. See our tutorial on installing add-on products with buildout for more information.