root/galaxy-central/tools/human_genome_variation/sift.xml @ 3

<tool id="hgv_sift" name="SIFT" version="1.0.0">
  <description>predictions of functional sites</description>

  <command interpreter="bash">
    sift_variants_wrapper.sh "$input" "$output" "${input.metadata.dbkey}" "${GALAXY_DATA_INDEX_DIR}/sift_db.loc" "$chrom_col" "$pos_col" "$base" "$allele_col" "$strand_source.strand_col" "$output_opts"
  </command>

  <inputs>
    <param name="input" type="data" format="tabular" label="Dataset">
      <validator type="unspecified_build"/>
      <validator type="dataset_metadata_in_file" filename="sift_db.loc" metadata_name="dbkey" metadata_column="0" message="Data is currently not available for the specified build."/>
    </param>
    <param name="chrom_col"  type="data_column" data_ref="input" label="Column with chromosome"/>
    <param name="pos_col"    type="data_column" data_ref="input" numerical="true" label="Column with position"/>
    <param name="base" type="select" label="Position coordinates are">
      <option value="0">zero-based</option>
      <option value="1" selected="true">one-based</option>
    </param>
    <param name="allele_col" type="data_column" data_ref="input" label="Column with allele"/>
    <conditional name="strand_source">
      <param name="choice" type="select" label="Strand info">
        <option value="data_column" selected="true">a column in the dataset</option>
        <option value="all_pos">all on sense/forward/+ strand</option>
        <option value="all_neg">all on antisense/reverse/- strand</option>
      </param>
      <when value="data_column">
        <param name="strand_col" type="data_column" data_ref="input" label="Column with strand"/>
      </when>
      <when value="all_pos">
        <param name="strand_col" type="hidden" value="+"/>
      </when>
      <when value="all_neg">
        <param name="strand_col" type="hidden" value="-"/>
      </when>
    </conditional>
    <param name="output_opts" type="select" multiple="true" display="checkboxes" label="Include the following additional fields in the output">
      <option value="A">Ensembl Gene ID</option>
      <option value="B">Gene Name</option>
      <option value="C">Gene Description</option>
      <option value="D">Ensembl Protein Family ID</option>
      <option value="E">Ensembl Protein Family Description</option>
      <option value="F">Ensembl Transcript Status (Known / Novel)</option>
      <option value="G">Protein Family Size</option>
      <option value="H">Ka/Ks (Human-mouse)</option>
      <option value="I">Ka/Ks (Human-macaque)</option>
      <option value="J">OMIM Disease</option>
      <option value="K">Allele Frequencies (All Hapmap Populations - weighted average)</option>
      <option value="L">Allele Frequencies (CEU Hapmap population)</option>
    </param>
  </inputs>

  <outputs>
    <data format="tabular" name="output" />
  </outputs>

  <requirements>
    <requirement type="binary">awk</requirement>
    <requirement type="binary">rm</requirement>
    <requirement type="binary">sed</requirement>
  </requirements>

  <tests>
    <test>
      <param name="input" value="sift_variants.tab" ftype="tabular" dbkey="hg18"/>
      <param name="chrom_col" value="1"/>
      <param name="pos_col" value="3"/>
      <param name="base" value="1"/>
      <param name="allele_col" value="5"/>
      <param name="choice" value="data_column"/>
      <param name="strand_col" value="4"/>
      <param name="output_opts" value="A"/>
      <output name="output" file="sift_variants_result.tab"/>
    </test>
  </tests>

  <help>
.. class:: warningmark

This currently works only for builds hg18 or hg19.

-----

**Dataset formats**

The input and output datasets are tabular_. 
(`Dataset missing?`_)

.. _tabular: ./static/formatHelp.html#tab
.. _Dataset missing?: ./static/formatHelp.html

-----

**What it does**

SIFT predicts whether an amino-acid substitution affects protein function,
based on sequence homology and the physical properties of amino acids.
SIFT can be applied to naturally occurring non-synonymous polymorphisms
and laboratory-induced missense mutations.  This tool uses SQLite databases
containing pre-computed SIFT scores and annotations for all possible nucleotide
substitutions at each position in the human exome.  Allele frequency data
are from the HapMap frequency database, and additional transcript and 
gene-level data are from Ensembl BioMart.

The input dataset must contain columns for the chromosome, position, and
alleles.  The alleles must be two nucleotides separated by '/',
usually the reference allele and the allele of interest.
The strand must either be in another column or all the same.
The output contains a standard set of columns plus the additional ones that
have been selected from the list above.

Website: http://sift.jcvi.org/

-----

**Example**

- input file::

    chr3   81780820   +  T/C
    chr2   230341630  +  G/A
    chr2   43881517   +  A/T
    chr2   43857514   +  T/C
    chr6   88375602   +  G/A
    chr22  29307353   -  T/A
    chr10  115912482  -  G/T
    chr10  115900918  -  C/T
    chr16  69875502   +  G/T
    etc.

- output file::

    #Chrom  Position   Strand  Allele  Codons   Transcript ID    Protein ID       Substitution  Region    dbSNP ID      SNP Type       Prediction  Score  Median Info  Num seqs at position  User Comment
    chr3    81780820   +       T/C     AGA-gGA  ENST00000264326  ENSP00000264326  R190G         EXON CDS  rs2229519:C   Nonsynonymous  DAMAGING    0.04   3.06         149
    chr2    230341630  +       G/T     -        ENST00000389045  ENSP00000373697  NA            EXON CDS  rs1803846:A   Unknown        Not scored  NA     NA           NA
    chr2    43881517   +       A/T     ATA-tTA  ENST00000260605  ENSP00000260605  I230L         EXON CDS  rs11556157:T  Nonsynonymous  TOLERATED   0.47   3.19         7
    chr2    43857514   +       T/C     TTT-TcT  ENST00000260605  ENSP00000260605  F33S          EXON CDS  rs2288709:C   Nonsynonymous  TOLERATED   0.61   3.33         6
    chr6    88375602   +       G/A     GTT-aTT  ENST00000257789  ENSP00000257789  V217I         EXON CDS  rs2307389:A   Nonsynonymous  TOLERATED   0.75   3.17         13
    chr22   29307353   +       T/A     ACC-tCC  ENST00000335214  ENSP00000334612  T264S         EXON CDS  rs42942:A     Nonsynonymous  TOLERATED   0.4    3.14         23
    chr10   115912482  +       C/A     CGA-CtA  ENST00000369285  ENSP00000358291  R179L         EXON CDS  rs12782946:T  Nonsynonymous  TOLERATED   0.06   4.32         2
    chr10   115900918  +       G/A     CAA-tAA  ENST00000369287  ENSP00000358293  Q271*         EXON CDS  rs7095762:T   Nonsynonymous  N/A         N/A    N/A          N/A
    chr16   69875502   +       G/T     ACA-AaA  ENST00000338099  ENSP00000337512  T608K         EXON CDS  rs3096381:T   Nonsynonymous  TOLERATED   0.12   3.41         3
    etc.

-----

**References**

Ng PC, Henikoff S. (2001) Predicting deleterious amino acid substitutions.
Genome Res. 11(5):863-74.

Ng PC, Henikoff S. (2002) Accounting for human polymorphisms predicted to affect protein function.
Genome Res. 12(3):436-46.

Ng PC, Henikoff S. (2003) SIFT: Predicting amino acid changes that affect protein function.
Nucleic Acids Res. 31(13):3812-4.

Kumar P, Henikoff S, Ng PC. (2009) Predicting the effects of coding non-synonymous variants
on protein function using the SIFT algorithm.
Nat Protoc. 4(7):1073-81. Epub 2009 Jun 25.

  </help>
</tool>