https://snicdocs.nsc.liu.se/w/index.php?title=ANNOVAR&feed=atom&action=history
ANNOVAR - Revision history
2024-03-28T16:36:19Z
Revision history for this page on the wiki
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https://snicdocs.nsc.liu.se/w/index.php?title=ANNOVAR&diff=2861&oldid=prev
Samuel Lampa (UPPMAX) at 08:24, 30 September 2011
2011-09-30T08:24:52Z
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 08:24, 30 September 2011</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|description=Functional annotation of genetic variants from high-throughput sequencing data  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|description=Functional annotation of genetic variants from high-throughput sequencing data  </div></td></tr>
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<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|fields=</div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|fields=<ins class="diffchange diffchange-inline">bioinformatics</ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[http://www.openbioinformatics.org/annovar/ ANNOVAR] is an efficient software tool to utilize update-to-date information to functionally annotate genetic variants detected from diverse genomes (including human genome hg18, hg19, as well as mouse, worm, fly, yeast and many others). Given a list of variants with chromosome, start position, end position, reference nucleotide and observed nucleotides, ANNOVAR can perform:</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[http://www.openbioinformatics.org/annovar/ ANNOVAR] is an efficient software tool to utilize update-to-date information to functionally annotate genetic variants detected from diverse genomes (including human genome hg18, hg19, as well as mouse, worm, fly, yeast and many others). Given a list of variants with chromosome, start position, end position, reference nucleotide and observed nucleotides, ANNOVAR can perform:</div></td></tr>
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Samuel Lampa (UPPMAX)
https://snicdocs.nsc.liu.se/w/index.php?title=ANNOVAR&diff=2858&oldid=prev
Samuel Lampa (UPPMAX): Created page with "__NOTOC__ {{software info |description=Functional annotation of genetic variants from high-throughput sequencing data |license=free |fields= }} [http://www.openbioinformatics.or..."
2011-09-30T08:14:23Z
<p>Created page with "__NOTOC__ {{software info |description=Functional annotation of genetic variants from high-throughput sequencing data |license=free |fields= }} [http://www.openbioinformatics.or..."</p>
<p><b>New page</b></p><div>__NOTOC__<br />
{{software info<br />
|description=Functional annotation of genetic variants from high-throughput sequencing data <br />
|license=free<br />
|fields=<br />
}}<br />
[http://www.openbioinformatics.org/annovar/ ANNOVAR] is an efficient software tool to utilize update-to-date information to functionally annotate genetic variants detected from diverse genomes (including human genome hg18, hg19, as well as mouse, worm, fly, yeast and many others). Given a list of variants with chromosome, start position, end position, reference nucleotide and observed nucleotides, ANNOVAR can perform:<br />
<br />
== Availability ==<br />
{{list resources for software}}<br />
<br />
== Tips and tricks ==<br />
* ...<br />
== License ==<br />
{{show license}}<br />
<br />
== Experts ==<br />
{{list experts}}<br />
<br />
== Links ==<br />
* [http://www.openbioinformatics.org/annovar/ Website]<br />
* [http://nar.oxfordjournals.org/content/38/16/e164 Publication]<br />
* [http://www.openbioinformatics.org/annovar/annovar_startup.html Manual]</div>
Samuel Lampa (UPPMAX)