Difference between revisions of "Nexalign"
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{{Bioinformatics application | {{Bioinformatics application | ||
|sw summary=Nexalign is a program to align millions of short reads from next-generation sequencing data sets to reference genomes | |sw summary=Nexalign is a program to align millions of short reads from next-generation sequencing data sets to reference genomes | ||
− | |bio method=Mapping, | + | |bio method=Mapping, |
− | |licence=GPL, | + | |licence=GPL, |
− | |os= | + | |os=UNIX, |
}} | }} | ||
{{Links}} | {{Links}} | ||
{{References}} | {{References}} | ||
+ | {{Link box}} |
Revision as of 11:54, 5 September 2011
Application data |
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Principal bioinformatics method(s) | Mapping |
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Maintained? | Maybe |
Licence | GPL |
Operating system(s) | UNIX |
Summary: Nexalign is a program to align millions of short reads from next-generation sequencing data sets to reference genomes
"Error: no local variable "counter" was set." is not a number.
Links
References
none specified
To add a reference for Nexalign, enter the PubMed ID in the field below and click 'Add'.
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Search for "Nexalign" in the SEQanswers forum / BioStar or:
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