Mercurial > repos > iuc > virheat
comparison macros.xml @ 0:1d509fa3ec39 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/virheat commit 5ae40d4f44fc2716f3c37a9fad2077a0d0230a6d
| author | iuc |
|---|---|
| date | Tue, 28 May 2024 11:06:59 +0000 |
| parents | |
| children | 259e86ec88e9 |
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| -1:000000000000 | 0:1d509fa3ec39 |
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| 1 <?xml version="1.0"?> | |
| 2 <macros> | |
| 3 <token name="@TOOL_VERSION@">0.7</token> | |
| 4 <token name="@VERSION_SUFFIX@">0</token> | |
| 5 <token name="@PROFILE@">21.01</token> | |
| 6 <xml name="biotools"> | |
| 7 <xrefs> | |
| 8 <xref type="bio.tools">virheat</xref> | |
| 9 </xrefs> | |
| 10 </xml> | |
| 11 <xml name="requirements"> | |
| 12 <requirements> | |
| 13 <requirement type="package" version="@TOOL_VERSION@">virheat</requirement> | |
| 14 <yield/> | |
| 15 </requirements> | |
| 16 </xml> | |
| 17 <xml name="version"> | |
| 18 <version_command>virheat --version</version_command> | |
| 19 </xml> | |
| 20 <token name="@HELP_HEADER@"><![CDATA[ | |
| 21 What it does | |
| 22 ============ | |
| 23 | |
| 24 This tool generates multi-sample variant-frequency plots from SnpEff-annotated | |
| 25 viral variant lists. The tool provides a condensed look at variant frequencies after mapping raw reads to a viral/bacterial reference genome and compares multiple vcf files at the same time. | |
| 26 | |
| 27 The tool expects either the length of a reference genome or the gff3 file if the sequence annotation is needed. | |
| 28 | |
| 29 Additionally, to analyze whether mutations are sufficiently covered and to display non-covered cells in grey, first create per-base coverage TSV files for each BAM file with Qualimap and provide them in the same folder as the VCF files. Give them the same name as your VCF files. | |
| 30 | |
| 31 Moreover, there is an option to include visualizations of additional scores (e.g., MAVE scores for binding affinity, expression level, antibody escape, etc.) mapped to mutations on the heatmap. | |
| 32 | |
| 33 The tool expects input variant lists in VCF format. VCF datasets as produced by standard variant callers with | |
| 34 | |
| 35 - variant allele frequencies encoded in an ``AF`` INFO field | |
| 36 - variant functional genomic effects annotated using SnpEff's EFF format | |
| 37 | |
| 38 ]]></token> | |
| 39 <xml name="citations"> | |
| 40 <citations> | |
| 41 <citation type="bibtex">@unpublished{Fuchs2020, | |
| 42 author = {Fuchs, Jonas}, | |
| 43 title = {}, | |
| 44 year = {2020}, | |
| 45 note = {Multi-sample annotated viral variant-frequency plots based on the R pheatmap package.}, | |
| 46 address = {Institute for Virology, University of Freiburg} | |
| 47 }</citation> | |
| 48 </citations> | |
| 49 </xml> | |
| 50 </macros> |
