databases > DOI:10.25504/FAIRsharing.w8wbyj

ready BRCA Share

General Information
BRCA Share is a novel gene datashare initiative that provides scientists and commercial laboratory organizations around the world with open access to BRCA Share (formerly UMD-BRCA1) contains BRCA1 and BRCA2 genetic data. The program’s goal is to accelerate research on BRCA gene mutations, particularly variants of uncertain significance, to improve the ability of clinical laboratory diagnostics to predict which individuals are at risk of developing these cancers.

Homepage http://www.umd.be/BRCA1/

Countries that developed this resource Belgium , France

Created in 1995

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How to cite this record FAIRsharing.org: BRCA Share; BRCA Share; DOI: https://doi.org/10.25504/FAIRsharing.w8wbyj; Last edited: Jan. 8, 2019, 1:15 p.m.; Last accessed: Apr 10 2021 4:31 p.m.


Record updated: Dec. 5, 2016, 11:31 a.m. by The FAIRsharing Team.

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no versioning but access to historical files is possible No link recorded

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manual curation No link recorded

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web interface No link recorded

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quarterly release No link recorded



Publications

Human Splicing Finder: an online bioinformatics tool to predict splicing signals.

Desmet FO., Hamroun D., Lalande M., Collod-Béroud G., Claustres M., Béroud C.,
Nucleic Acids Res. 2009

View Paper (PubMed)

UMD (Universal mutation database): a generic software to build and analyze locus-specific databases.

Béroud C., Collod-Béroud G., Boileau C., Soussi T., Junien C.,
Hum. Mutat. 2000

View Paper (PubMed)

UMD (Universal Mutation Database): 2005 update.

Béroud C., Hamroun D., Collod-Béroud G., Boileau C., Soussi T., Claustres M.,
Hum. Mutat. 2005

View Paper (PubMed)

Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases.

Caputo S,Benboudjema L,Sinilnikova O,Rouleau E,Beroud C,Lidereau R
Nucleic Acids Res 2011

View Paper (PubMed) View Publication

UMD-predictor, a new prediction tool for nucleotide substitution pathogenicity -- application to four genes: FBN1, FBN2, TGFBR1, and TGFBR2.

Frédéric MY., Lalande M., Boileau C., Hamroun D., Claustres M., Béroud C., Collod-Béroud G.,
Hum. Mutat. 2009

View Paper (PubMed)

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Grant Number(s)

  • 200754 (European Commission FP7)