Novoalign (DISABLED - will be removed 9/28/2017)

NOTE: Due to lack of use, this software module has been disabled and will be removed from MSI systems on 9/28/2017. If you need this software, please contact help@msi.umn.edu.
 
Novoalign is a highly accurate program for mapping next-generation sequencing reads to a reference database. It is an aligner for single-ended and paired-end reads from the Illumina Genome Analyser. Novoalign finds global optimum alignments using full Needleman-Wunsch algorithm with affine gap penalties.
 
To run this software interactively in a Linux environment run the commands:
module load novoalign
novoindex indexfile sequencefiles
novoalign -d indexfile

For documentation, run a command without parameters, or refer to the Novoalign homepage.

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