| Previous changeset 14:5c852eca82e0 (2018-02-28) Next changeset 16:07e71cf6c8ef (2018-04-03) |
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Commit message:
planemo upload for repository https://github.com/blankenberg/tools-blankenberg/tree/master/tools/naive_variant_caller commit dfca863a9a361877d6d98b92072f1ebc316c5767 |
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modified:
naive_variant_caller.xml |
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| diff -r 5c852eca82e0 -r aff38ea879f1 naive_variant_caller.xml --- a/naive_variant_caller.xml Wed Feb 28 15:54:57 2018 -0500 +++ b/naive_variant_caller.xml Wed Feb 28 16:01:52 2018 -0500 |
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| @@ -1,4 +1,4 @@ -<tool id="naive_variant_caller" name="Naive Variant Caller" version="0.0.3"> +<tool id="naive_variant_caller" name="Naive Variant Caller (NVC)" version="0.0.3"> <description> - tabulate variable sites from BAM datasets</description> <requirements> <requirement type="package" version="0.0.3">nvc</requirement> @@ -147,6 +147,10 @@ </test> </tests> <help> +The **Naive Variant Caller** tool (NVC). + +------ + **What it does** This tool is a naive variant caller that processes aligned sequencing reads from the BAM format and produces a VCF file containing per position variant calls. This tool allows multiple BAM files to be provided as input and utilizes read group information to make calls for individual samples. |