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Navigation: Home
\ Graphic Apps
\ CAD \ VarScan
VarScan2.4.6 by Dan Koboldt |
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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. VarScan is a platform-independent, technology-independent software tool for identifying SNPs and indels in massively parallel sequencing of individual and pooled samples. Given data for a single sample, VarScan identifies and filters germline ...
type: Open Source
Download VarScancategories: SNP identifier, identify SNP, filter variant, identify, identifier, SNP Add to Download Basket Report virus or spyware |
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| Software Info | |
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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but some information may be out-of-date.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! |
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| 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 |
| Install | Instal And Uninstall |
| Add Your Review or Windows Vista Compatibility Report |
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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