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Navigation: Home \ Graphic Apps \ CAD \ VarScan

VarScan

 2.4.6   by Dan Koboldt

Vista Compatible
Software Description:
The advent of massively parallel sequencing technologies has fundamentally changed the study of genetics. New platforms like the Illumina GAIIx and the Roche GS yield unprecedented levels of sequencing throughput. The analysis and interpretation of data from next-generation sequencing platforms presents a substantial informatics challenge. ...
type: Open Source
categories: SNP identifier, identify SNP, filter variant, identify, identifier, SNP
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Software Info
Best Vista Download periodically updates pricing and software information of VarScan full version from the publisher, but some information may be out-of-date. You should confirm all information.
Software piracy is theft, using crack, warez passwords, patches, serial numbers, registration codes, key generator, keymaker or keygen for VarScan license key is illegal and prevent future development of VarScan. Download links are directly from our mirrors or publisher's website, VarScan torrent files or shared files from rapidshare, yousendit or megaupload are not allowed!
Released: March 28, 2023
Filesize: 123 kB
Platform: Windows XP, Windows Vista, Windows Vista x64, Windows 7, Windows 7 x64, Windows 8, Windows 8 x64, Windows 10, Windows 10 x64, Windows 11, Linux, Mac OS X
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VarScan

- Releases History
Software: VarScan 2.4.6
Date Released: Mar 28, 2023
Status: New Release
Software: VarScan 2.3.8
Date Released: May 13, 2015
Status: New Release
Release Notes: VarScan v2.3.8 now incorporates false-positive filtering! This works for single-sample variant calls
or somatic/LOH/germline calls from the somatic command. Both native VarScan output format and VCF
format variant files are supported. SNVs and indels are both supported.
This new command replaces the functionality of the fpfilter.pl accessory script.
Software: VarScan 2.3.7
Date Released: Jul 22, 2014
Status: New Release
Release Notes: Fixed the issue of zero-depth lines in single-sample pileups for VarScan copynumber
Fixed a similar issue causing inconsistent column output for multi-sample mpileups in VarScan mpileup2*
Multi-sample VCFs generated with VarScan v2.3.6 and earlier might be missing sample columns.


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VarScan 2.4.6 download by Dan Koboldt
... of each variant (Germline, Somatic, or LOH) by comparing read counts between samples. FEATURES: · Calls SNPs and Indels from SAMtools pileup files · Filters variants by ...
type: Open Source
categories: SNP identifier, identify SNP, filter variant, identify, identifier, SNP
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