# HG changeset patch # User chrisw # Date 1574140999 0 # Node ID f84a4ffe8bd7d8345e7adcba4ba25db2aeeb040b # Parent 8e9a8987581c21a58b2c3774d04ea087dbdfc977 Uploaded diff -r 8e9a8987581c -r f84a4ffe8bd7 tool_dependencies.26.xml --- a/tool_dependencies.26.xml Tue Nov 19 05:21:33 2019 +0000 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,76 +0,0 @@ - - - - - - - - https://github.com/BenLangmead/bamcount/releases/download/0.2.6/bamcount-0.2.6.zip - - . - $INSTALL_DIR - - - - $INSTALL_DIR - - - - [options] - -Options: - -h --help Show this screen. - --version Show version. - --threads # of threads to do BAM decompression - -Non-reference summaries: - --alts Print differing from ref per-base coverages - Writes to a CSV file .alts.tsv - --include-softclip Print a record for soft-clipped bases - --include-n Print mismatch records when mismatched read base is N - --print-qual Print quality values for mismatched bases - --delta Print POS field as +/- delta from previous - --require-mdz Quit with error unless MD:Z field exists everywhere it's - expected - --no-head Don't print sequence names and lengths in header - -Coverage and quantification: - --coverage Print per-base coverage (slow but totally worth it) - --auc Print per-base area-under-coverage, will generate it for the genome - and for the annotation if --annotation is also passed in - Writes to a TSV file .auc.tsv - --bigwig Output coverage as BigWig file(s). Writes to .all.bw - (also .unique.bw when --min-unique-qual is specified). - Requires libBigWig. - --annotation - Path to BED file containing list of regions to sum coverage over - (tab-delimited: chrm,start,end) - --min-unique-qual - Output second bigWig consisting built only from alignments - with at least this mapping quality. --bigwig must be specified. - Also produces second set of annotation sums based on this coverage - if --annotation is enabled - --double-count Allow overlapping ends of PE read to count twice toward - coverage - --num-bases Report total sum of bases in alignments processed (that pass filters) - -Other outputs: - --read-ends Print counts of read starts/ends, if --min-unique-qual is set - then only the alignments that pass that filter will be counted here - Writes to 2 TSV files: .starts.tsv, .ends.tsv - --frag-dist Print fragment length distribution across the genome - Writes to a TSV file .frags.tsv - --echo-sam Print a SAM record for each aligned read - --ends Report end coordinate for each read (useful for debugging) - ]]> - -