Mercurial > repos > iuc > virheat
diff 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 |
line wrap: on
line diff
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/macros.xml Tue May 28 11:06:59 2024 +0000 @@ -0,0 +1,50 @@ +<?xml version="1.0"?> +<macros> + <token name="@TOOL_VERSION@">0.7</token> + <token name="@VERSION_SUFFIX@">0</token> + <token name="@PROFILE@">21.01</token> + <xml name="biotools"> + <xrefs> + <xref type="bio.tools">virheat</xref> + </xrefs> + </xml> + <xml name="requirements"> + <requirements> + <requirement type="package" version="@TOOL_VERSION@">virheat</requirement> + <yield/> + </requirements> + </xml> + <xml name="version"> + <version_command>virheat --version</version_command> + </xml> + <token name="@HELP_HEADER@"><![CDATA[ +What it does +============ + +This tool generates multi-sample variant-frequency plots from SnpEff-annotated +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. + +The tool expects either the length of a reference genome or the gff3 file if the sequence annotation is needed. + +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. + +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. + +The tool expects input variant lists in VCF format. VCF datasets as produced by standard variant callers with + + - variant allele frequencies encoded in an ``AF`` INFO field + - variant functional genomic effects annotated using SnpEff's EFF format + +]]></token> + <xml name="citations"> + <citations> + <citation type="bibtex">@unpublished{Fuchs2020, + author = {Fuchs, Jonas}, + title = {}, + year = {2020}, + note = {Multi-sample annotated viral variant-frequency plots based on the R pheatmap package.}, + address = {Institute for Virology, University of Freiburg} + }</citation> + </citations> + </xml> +</macros>
