Mercurial > repos > saketkc > condel
diff tools/condel/condel_web.xml @ 0:742c7ee37f8b
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author | Saket Choudhary <saketkc@gmail.com> |
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date | Wed, 20 Nov 2013 00:48:30 +0530 |
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children | 5915ae11d9cd |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tools/condel/condel_web.xml Wed Nov 20 00:48:30 2013 +0530 @@ -0,0 +1,35 @@ +<tool id="condel_web" name="condel"> + <description>Condel web service</description> + <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> + <help> + **What it does** + 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. + Condel was developed to integrate the outputs of five 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 + + + 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 Galaxy tool in work leading to a scientific publication 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> +