Difference between revisions of "NextGENe"

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m (Text replace - "SNP discovery" to "SNP detection")
m (Text replace - "InDel discovery" to "Indel detection")
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{{Bioinformatics application
 
{{Bioinformatics application
 
|sw summary=de novo and reference assembly of Roche/454, Illumina and SOLiD data. Uses a novel Condensation Assembly Tool approach where reads are joined via "anchors" into mini-contigs before assembly which reduces sequencing errors. Requires Win or MacOS.
 
|sw summary=de novo and reference assembly of Roche/454, Illumina and SOLiD data. Uses a novel Condensation Assembly Tool approach where reads are joined via "anchors" into mini-contigs before assembly which reduces sequencing errors. Requires Win or MacOS.
|bio domain=Sequence assembly (de novo assembly), Metagenomics, SNP detection, InDel discovery, Targeted resequencing,  
+
|bio domain=Sequence assembly (de novo assembly), Metagenomics, SNP detection, Indel detection, Targeted resequencing,  
 
|bio tech=Illumina, 454, ABI SOLiD
 
|bio tech=Illumina, 454, ABI SOLiD
 
|created at=SoftGenetics LLC
 
|created at=SoftGenetics LLC

Revision as of 19:56, 19 December 2015

Application data

Biological application domain(s) Sequence assembly (de novo assembly), Metagenomics, SNP detection, Indel detection, Targeted resequencing
Technology Illumina, 454, ABI SOLiD
Created at SoftGenetics LLC
Maintained? Yes
Input format(s) FASTQ, FASTA, Scarf, FNAQual, CSFASTA/CSQUAL (ABI SOLiD)
Software features Unique condensation tool, Data Visualisation, very flexible
Programming language(s) C++
Licence Commercial
Operating system(s) Windows

Summary: de novo and reference assembly of Roche/454, Illumina and SOLiD data. Uses a novel Condensation Assembly Tool approach where reads are joined via "anchors" into mini-contigs before assembly which reduces sequencing errors. Requires Win or MacOS.

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Link: http://softgenetics.com/NextGENe.html Category: Integrated solutions

Links

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References

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