Open main menu

SEQwiki β

Nexalign

Revision as of 13:33, 23 September 2011 by Andreas.sjodin (talk | contribs)

Application data

Created by Timo Lassmann
Principal bioinformatics method(s) Mapping
Technology 454, SOLiD, Illumina
Created at RIKEN Yokohama Institute
Maintained? No
Input format(s) FASTA
Output format(s) BED, GFF, TXT
Programming language(s) C++, R
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'.