Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Updating tools/bwameth from version 0.2.6 to 0.2.7 #5262

Merged
merged 5 commits into from
Jun 2, 2024
Merged
Changes from 3 commits
Commits
File filter

Filter by extension

Filter by extension

Conversations
Failed to load comments.
Loading
Jump to
Jump to file
Failed to load files.
Loading
Diff view
Diff view
7 changes: 4 additions & 3 deletions tools/bwameth/bwameth.xml
Original file line number Diff line number Diff line change
@@ -1,7 +1,7 @@
<tool id="bwameth" name="bwameth" version="@TOOL_VERSION@+galaxy0" profile="20.05">
<description>Fast and accurate aligner of BS-Seq reads.</description>
<macros>
<token name="@TOOL_VERSION@">0.2.6</token>
<token name="@TOOL_VERSION@">0.2.7</token>
</macros>
<requirements>
<requirement type="package" version="@TOOL_VERSION@">bwameth</requirement>
Expand Down Expand Up @@ -78,7 +78,8 @@ bwameth.py
#else:
$read1 $read2
#end if
| samtools view --no-PG -u - | samtools sort --no-PG -@ "\${GALAXY_SLOTS:-4}" -T "\${TMPDIR:-.}" -O bam -o output.bam -
| samtools sort -@\${GALAXY_SLOTS:-4} -T "\${TMPDIR:-.}" -O bam -o output.bam
Copy link
Contributor

Choose a reason for hiding this comment

The reason will be displayed to describe this comment to others. Learn more.

Please undo this change and maybe add the explanation from here

## Convert SAM output to sorted BAM

Maybe use exactly the command line from over there:

| samtools sort --no-PG -l 0 -T "\${TMPDIR:-.}" -O bam | samtools view --no-PG -O bam -@ \${GALAXY_SLOTS:-1} -o output.bam


]]></command>
<inputs>
<conditional name="referenceSource">
Expand Down Expand Up @@ -153,7 +154,7 @@ bwameth.py

**What it does**

BWA-meth performs alignment of reads in a bisulfite-sequencing experiment (e.g., RRBS or WGBS) to a genome. The methodology employed for this is similar to bismark, where both the reads and the reference genome are *in silico* converted prior to alignment. Methylation extraction on the resulting BAM file can be done with the PileOMeth tool.
BWA-meth performs the alignment of reads in a bisulfite-sequencing experiment (e.g., RRBS or WGBS) to a genome. This methodology is similar to bismark, where both the reads and the reference genome are *in silico* converted prior to alignment. Methylation extraction on the resulting BAM file can be done with the PileOMeth tool.
]]></help>
<citations>
<citation type="bibtex">@misc{1401.1129,
Expand Down