Difference between revisions of "CLCbio Genomics Workbench"

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{{Bioinformatics application
 
{{Bioinformatics application
 
|sw summary=de novo and reference assembly of Sanger, 454, Solexa, Helicos, and SOLiD data. Commercial next-gen-seq software that extends the CLCbio Main Workbench software. Includes SNP detection, browser and other features. Runs on Windows, Mac OS X and Linux.
 
|sw summary=de novo and reference assembly of Sanger, 454, Solexa, Helicos, and SOLiD data. Commercial next-gen-seq software that extends the CLCbio Main Workbench software. Includes SNP detection, browser and other features. Runs on Windows, Mac OS X and Linux.
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|bio domain=Genomics, Whole Genome Resequencing, De-novo assembly, SNP discovery, InDel discovery, ChIP-Seq, InDel discovery, RNA-Seq,
 
}}
 
}}
 
Link: http://www.clcbio.com/index.php?id=1240 Category: Integrated solutions
 
Link: http://www.clcbio.com/index.php?id=1240 Category: Integrated solutions

Revision as of 07:04, 13 January 2010

Application data

Biological application domain(s) Genomics, Whole Genome Resequencing, De-novo assembly, SNP discovery, InDel discovery, ChIP-Seq, InDel discovery, RNA-Seq
Maintained? Maybe

Summary: de novo and reference assembly of Sanger, 454, Solexa, Helicos, and SOLiD data. Commercial next-gen-seq software that extends the CLCbio Main Workbench software. Includes SNP detection, browser and other features. Runs on Windows, Mac OS X and Linux.

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Link: http://www.clcbio.com/index.php?id=1240 Category: Integrated solutions