VariantMaster Files

Extract causative variants for monogenic and sporadic genetic diseases

Brought to you by: fredsanto

The interactive file manager requires Javascript. Please enable it or use sftp or scp.
You may still browse the files here.

Name	Modified	Size	InfoDownloads / Week
Parent folder
variantMaster_1.01.gz	2014-05-05	15.3 MB	0
VariantMaster_1.0.gz	2014-05-05	15.5 MB	0
Totals: 2 Items		30.8 MB	0

VariantMaster release 1.02 -------------------------
- Python package
- Recessive model improved

VariantMaster release 1.01 ------------------------- 
- Works with Annovar postAug2013 versions

VariantMaster release 1.0 ------------------------- 
- Precompiled version - gunzip and use -- Linux 64bit only 
- Works with Annovar preAug2013 versions

Source: README.txt, updated 2014-05-05

Other Useful Business Software

Get Avast Free Antivirus with 24/7 AI-powered online scam detection

Get protection for today’s online threats. Free.

Award-winning antivirus protection, as well as protection against online scams, dangerous Wi-Fi connections, hacked accounts, and ransomware. It includes Avast Assistant, your built-in AI partner, which gives you help with suspicious online messages, offers, and more.

Learn More

Our Free Plans just got better! | Auth0

With up to 25k MAUs and unlimited Okta connections, our Free Plan lets you focus on what you do best—building great apps.

You asked, we delivered! Auth0 is excited to expand our Free and Paid plans to include more options so you can focus on building, deploying, and scaling applications without having to worry about your security. Auth0 now, thank yourself later.

Try free now

Recommended Projects

Atlas2
Atlas is a suite of variant analysis tools specializing in the separation of true SNPs and insertions and deletions (indels) from sequencing and mapping errors in Whole Exome Capture Sequecing (WECS) data.
DeNovoGear
DeNovoGear is a program to detect denovo mutations using sequencing data. The methods behind DeNovoGear are described in this publication, http://www.nature.com/nmeth/journal/v10/n10/full/nmeth.2611.html The production version of the code(updated more frequently) can be found here, https://github.com/denovogear/denovogear The releases of major and minor versions of the code are this Sourceforge page.
snpEff
snpEff is a fast variant effect predictor (SNP, MNP and InDels) for genomic data. It is integrated with Galaxy so it can be used either as a command line or as a web application.

VariantMaster Files

Extract causative variants for monogenic and sporadic genetic diseases

Get an email when there's a new version of VariantMaster