bio-samtools-wrapper 2.7.0
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- data/README.md +501 -0
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- data/lib/bio/db/alignment.rb +64 -0
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- data/lib/bio/db/pileup.rb +273 -0
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- data/lib/bio-samtools-wrapper.rb +9 -0
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- data/test/test_bio-samtools-wrapper.rb +1 -0
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class Bio::DB
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<h3>Table of Contents</h3>
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<li><a href="#module-Bio-label-Bio%3A%3ADB%3A%3APileup+">Bio::DB::Pileup </a>
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<li><a href="#module-Bio-label-Vcf+">Vcf </a>
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module Bio
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<h1 id="module-Bio-label-Bio%3A%3ADB%3A%3APileup+"><a href="Bio/DB/Pileup.html">Bio::DB::Pileup</a> <span><a href="#module-Bio-label-Bio%3A%3ADB%3A%3APileup+">¶</a> <a href="#documentation">↑</a></span></h1>
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<p>A class representing information in SAMTools pileup format</p>
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<dl class="rdoc-list note-list"><dt>Author
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<dd>
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<p>Dan MacLean (dan.maclean@tsl.ac.uk)</p>
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</dd></dl>
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<p>Pileup is described at <a
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href="http://sourceforge.net/apps/mediawiki/samtools/index.php?title=SAM_FAQ#I_do_not_understand_the_columns_in_the_pileup_output">sourceforge.net/apps/mediawiki/samtools/index.php?title=SAM_FAQ#I_do_not_understand_the_columns_in_the_pileup_output</a>.
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Briefly (when you invoke pileup with the -c option):</p>
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<ul><li>
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<p>1 reference sequence name</p>
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</li><li>
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<p>2 reference coordinate</p>
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</li><li>
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<p>(3) reference base, or `*' for an indel line</p>
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</li><li>
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<p>(4) genotype where heterozygotes are encoded in the IUB code: M=A/C, R=A/G,
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W=A/T, S=C/G, Y=C/T and K=G/T; indels are indicated by, for example, +A,
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-A or +CC/-C. There is no difference between */+A or +A/*.</p>
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</li><li>
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<p>(5) Phred-scaled likelihood that the genotype is wrong, which is also
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called `consensus quality'.</p>
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</li><li>
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<p>(6) Phred-scaled likelihood that the genotype is identical to the
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reference, which is also called `SNP quality'. Suppose the reference
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base is A and in alignment we see 17 G and 3 A. We will get a low consensus
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quality because it is difficult to distinguish an A/G heterozygote from a
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G/G homozygote. We will get a high SNP quality, though, because the
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evidence of a SNP is very strong.</p>
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</li><li>
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<p>(7) root mean square (RMS) mapping quality</p>
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</li><li>
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<p>8 # reads covering the position</p>
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</li><li>
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<p>9 read bases at a SNP line (check the manual page for more information);
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the 1st indel allele otherwise</p>
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</li><li>
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<p>10 base quality at a SNP line; the 2nd indel allele otherwise</p>
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</li><li>
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<p>(11) indel line only: # reads directly supporting the 1st indel allele</p>
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</li><li>
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<p>(12) indel line only: # reads directly supporting the 2nd indel allele</p>
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</li><li>
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<p>(13) indel line only: # reads supporting a third indel allele</p>
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</li></ul>
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<p>If pileup is invoked without `-c', indel lines and columns between 3
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and 7 inclusive will not be outputted.</p>
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<p>NB mpileup uses the 6 column output format eg
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“seq2t151tGtGt36t0t99t12t.….……At:9<;;7=<<<<<” Pileup
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provides accessors for all columns (6 or 10 column format) and a few other
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useful methods</p>
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<p>require 'rubygems' require'ffi' require
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'bio/db/sam/bam'</p>
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<h1 id="module-Bio-label-Vcf+">Vcf <span><a href="#module-Bio-label-Vcf+">¶</a> <a href="#documentation">↑</a></span></h1>
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<p>A class representing information in Variant Call Format Forked from vcfruby
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at <a
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href="https://github.com/jesserod/vcfruby">github.com/jesserod/vcfruby</a>
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