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
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Application data |
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| Principal bioinformatics method(s) | Mapping |
|---|---|
| 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'.
[ edit box ]
Search for "Nexalign" in the SEQanswers forum / BioStar or:
| Web Search | Wiki Sites | Scientific |
|---|---|---|
