Difference between revisions of "GapFiller"
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{{#if: {{#var: citation}}|==Citation== | {{#if: {{#var: citation}}|==Citation== | ||
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| + | Marten Boetzer and Walter Pirovano. ''Toward almost closed genomes with GapFiller''. Genome Biology 2012, 13:R56. [ [http://genomebiology.com/2012/13/6/R56 web] ] | ||
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Revision as of 19:23, 13 March 2014
Description
GapFiller is an automated tool to reliably close gaps within scaffolds using paired reads.
De novo assembly is a commonly used application of next-generation sequencing experiments. The ultimate goal is to puzzle millions of reads into one complete genome, although draft assemblies usually result in a number of gapped scaffold sequences. The GapFiller method shows good results on both bacterial and eukaryotic datasets, allowing only few errors. As a consequence, the amount of additional wetlab work needed to close a genome is drastically reduced.
Required Modules
Serial
- gapfiller
System Variables
- HPC_{{#uppercase:gapfiller}}_DIR
Citation
If you publish research that uses gapfiller you have to cite it as follows:
Marten Boetzer and Walter Pirovano. Toward almost closed genomes with GapFiller. Genome Biology 2012, 13:R56. [ web ]