Workflow Entry: The NOTCH2 workflow

Created at: 06/09/11 @ 09:24:22      Last updated: 06/09/11 @ 09:26:48
Information Version 1 (of 1)

Version created on: 06/09/11 @ 09:24:22 by: Pierre Lindenbaum   |   Revision comments Expand

Last edited on: 06/09/11 @ 09:26:48 by: Pierre Lindenbaum

Title: The NOTCH2 workflow

Type: KNIME


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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.

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Version History

Earliest Version:
[1] - The NOTCH2 workflow

Created on: Tuesday 06 September 2011 @ 09:24:22 (GMT)

Created by: Pierre Lindenbaum

Last edited on: Tuesday 06 September 2011 @ 09:26:48 (GMT)

Last edited by: Pierre Lindenbaum

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Non-Information Resource URI: http://www.myexperiment.org/workflows/2320


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