Mercurial > repos > xuebing > sharplabtool
diff tools/human_genome_variation/funDo.xml @ 0:9071e359b9a3
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author | xuebing |
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date | Fri, 09 Mar 2012 19:37:19 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tools/human_genome_variation/funDo.xml Fri Mar 09 19:37:19 2012 -0500 @@ -0,0 +1,101 @@ +<tool id="hgv_funDo" name="FunDO" version="1.0.0"> + <description>human genes associated with disease terms</description> + + <command interpreter="perl"> + disease_ontology_gene_fuzzy_selector.pl $build $out_file1 ${GALAXY_DATA_INDEX_DIR}/funDo.loc '$term' + </command> + + <inputs> + <param name="build" type="select" label="Database build"> + <options from_file="funDo.loc"> + <column name="name" index="0"/> + <column name="value" index="0"/> + <filter type="unique_value" column="0"/> + </options> + </param> + <param name="term" size="40" type="text" label="Disease term(s)" /> + </inputs> + + <outputs> + <data format="interval" name="out_file1"> + </data> + </outputs> + + <tests> + <test> + <param name="term" value="lung"/> + <param name="build" value="hg18"/> + <output name="out_file1" file="funDo_output1.interval" /> + </test> + </tests> + + <help> +**Dataset formats** + +There is no input dataset. The output is in interval_ format. + +.. _interval: ./static/formatHelp.html#interval + +----- + +**What it does** + +This tool searches the disease-term field of the DOLite mappings +used by the FunDO project and returns a set of genes that +are associated with terms matching the specified pattern. (This is the +reverse of what FunDO's own server does.) + +The search is case insensitive, and selects terms that contain any of +the given words, either exactly or within a longer word (e.g. "nemia" +selects not only "anemia", but also "hyperglycinemia", "tyrosinemias", +and many other things). Multiple words should be separated by spaces, +not commas. As a special case, entering the word "disease" returns all +genes associated with any disease, even if that word does not actually +appear in the term field. + +Website: http://django.nubic.northwestern.edu/fundo/ + +----- + +**Example** + +Typing:: + + carcinoma + +results in:: + + 1. 2. 3. 4. 5. 6. 7. + chr11 89507465 89565427 + NAALAD2 10003 Adenocarcinoma + chr15 50189113 50192264 - BCL2L10 10017 Carcinoma + chr7 150535855 150555250 - ABCF2 10061 Clear cell carcinoma + chr7 150540508 150555250 - ABCF2 10061 Clear cell carcinoma + chr10 134925911 134940397 - ADAM8 101 Adenocarcinoma + chr10 134925911 134940397 - ADAM8 101 Adenocarcinoma + etc. + +where the column contents are as follows:: + + 1. chromosome name + 2. start position of the gene + 3. end position of the gene + 4. strand + 4. gene name + 6. Entrez Gene ID + 7. disease term + +----- + +**References** + +Du P, Feng G, Flatow J, Song J, Holko M, Kibbe WA, Lin SM. (2009) +From disease ontology to disease-ontology lite: statistical methods to adapt a general-purpose +ontology for the test of gene-ontology associations. +Bioinformatics. 25(12):i63-8. + +Osborne JD, Flatow J, Holko M, Lin SM, Kibbe WA, Zhu LJ, Danila MI, Feng G, Chisholm RL. (2009) +Annotating the human genome with Disease Ontology. +BMC Genomics. 10 Suppl 1:S6. + + </help> +</tool>