https://snicdocs.nsc.liu.se/w/index.php?action=history&feed=atom&title=ANFO 2026-04-08T00:28:40Z Revision history for this page on the wiki MediaWiki 1.31.10 https://snicdocs.nsc.liu.se/w/index.php?title=ANFO&diff=2847&oldid=prev 2011-09-29T14:00:18Z

<p>Created page with &quot;__NOTOC__ {{software info |description=A parallel assembler for short read sequence data |license=free |fields=bioinformatics }} == Availability == {{list resources for software...&quot;</p> <p><b>New page</b></p><div>__NOTOC__<br /> {{software info<br /> |description=A parallel assembler for short read sequence data <br /> |license=free<br /> |fields=bioinformatics<br /> }}<br /> == Availability ==<br /> {{list resources for software}}<br /> <br /> == License ==<br /> {{show license}}<br /> <br /> == Experts ==<br /> {{list experts}}<br /> <br /> Anfo is a short read aligner for cases where the DNA sequence is modified compared to the reference. <br /> <br /> == Publisher ==<br /> Udo Stenzel, Max Planck Institute for Evolutionary Anthropology<br /> * '''Website:''' http://bioinf.eva.mpg.de/anfo/</div>

Samuel Lampa (UPPMAX)