Mercurial > repos > saketkc > condel
diff condel_web/condel_web.xml @ 3:65a71127f1fa draft
Uploaded
| author | saketkc |
|---|---|
| date | Mon, 14 Apr 2014 21:20:43 -0400 |
| parents | |
| children | 328c3e782d31 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/condel_web/condel_web.xml Mon Apr 14 21:20:43 2014 -0400 @@ -0,0 +1,50 @@ +<tool id="condel_web" name="condel"> + <description>Condel web service</description> + <requirements> + <requirement type="package" version="2.2.1">requests</requirement> + <requirement type="python-module">requests</requirement> + </requirements> + <command interpreter="python"> + condel_web.py --input $input --output $output + </command> + <inputs> + <param name="input" format="text" type="data" label="Input Variants" /> + </inputs> + <outputs> + <data name="output" format="tabular"/> + </outputs> + <tests> + <test> + <param name="input" value="condel_input.txt"/> + <output name="output" file="condel_output.txt"/> + </test> + </tests> + <help> + **What it does** + + This script calls condel web api at http://bg.upf.edu/condel/ + + Condel stands for CONsensus DELeteriousness score of non-synonymous single nucleotide variants (SNVs). + The idea behind it is to integrate the output of computational tools aimed at assessing the impact of non synonymous SNVs on protein function. + To do this, it computes a weighted average of the scores (WAS) of these tools : SIFT, Polyphen2, MAPP, LogR Pfam E-value + (implemented ad hoc following the instructions at Clifford RJ, Edmonson MN, Nguyen C, and Buetow KH (2004) + Large-scale analysis of non-synonymous coding region single nucleotide polymorphisms. Bioinformatics 20, 1006-1014) and MutationAssessor + + **How does it work** + + The scores of different methods are weighted using the complementary cumulative distributions produced by the five methods on a + dataset of approximately 20000 missense SNPs, both deleterious and neutral. The probability that a predicted deleterious mutation is not a + false positive of the method and the probability that a predicted neutral mutation is not a false negative are employed as weights. + + **Citation** + + + If you use this tool please cite: + + + Improving the Assessment of the Outcome of Nonsynonymous SNVs with a Consensus Deleteriousness Score, Condel (2011) Abel González-Pérez and Nuria López-Bigas, American Journal of Human Genetics 10.1016/j.ajhg.2011.03.004 + + + </help> +</tool> +
