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Created: 03/03/09 @ 13:17:27 | Last updated: 02/11/09 @ 10:13:38
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License: Creative Commons Attribution-Share Alike 3.0 Unported License
This workflow searches OMIM for entries associated with a particular disease in OMIM, returns the IDs and maps them to Kegg Gene IDs. For each gene, it then gets the description and any corresponding pathways those genes are involved with
Rating: 4.0 / 5 (1 rating) | Versions: 2 | Reviews: 0 | Comments: 0 | Citations: 0 Viewed: 93 times | Downloaded: 35 times Tags (9): |
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Created: 06/09/11 @ 09:24:22 | Last updated: 06/09/11 @ 09:26:48
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License: Creative Commons Attribution-Share Alike 3.0 Unported License
Analysis of the exome sequencing data for the following article:
Nat Genet. 2011 Mar 6;43(4):306-8.
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis.
Isidor B, Lindenbaum P, Pichon O, Bézieau S, Dina C, Jacquemont S, Martin-Coignard D, Thauvin-Robinet C, Le Merrer M, Mandel JL, David A, Faivre L, Cormier-Daire V, Redon R, Le Caignec C.
using knime4bio
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Created: 08/02/12 @ 16:08:08 | Last updated: 09/05/12 @ 09:52:18
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License: Creative Commons Attribution-Share Alike 3.0 Unported License
Defines regions and genes from associated SNPs
A JAVA MySQL connector is required to run the workflow and must be placed in the $TAVERNA_HOME/lib directory.
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