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RRID:SCR_006552 RRID Copied    
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Resource Information

URL: http://decipher.sanger.ac.uk/

Description: Interactive database which incorporates a suite of tools designed to aid the interpretation of submicroscopic chromosomal imbalance. Used to enhance clinical diagnosis by retrieving information from bioinformatics resources relevant to the imbalance found in the patient. Contributing to the DECIPHER database is a Consortium, comprising an international community of academic departments of clinical genetics. Each center maintains control of its own patient data (which are password protected within the center''''s own DECIPHER project) until patient consent is given to allow anonymous genomic and phenotypic data to become freely viewable within Ensembl and other genome browsers. Once data are shared, consortium members are able to gain access to the patient report and contact each other to discuss patients of mutual interest, thus facilitating the delineation of new microdeletion and microduplication syndromes.

Resource Name: DECIPHER

Proper Citation: DECIPHER (RRID:SCR_006552)

Resource Type: Resource, data or information resource, database

Keywords: chromosomal imbalance, phenotype, chromosome, gene, genome, deletion, duplication, copy number, genotype, polymorphism

Resource ID: SCR_006552

Parent Organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom

Related Condition: Developmental disorder, Microdeletion Syndrome, Overgrowth syndrome, Microduplication syndrome, Deletion syndrome, Duplication syndrome, Wolf-Hirschhorn Syndrome, Williams-Beuren Syndrome, Smith-Magenis Syndrome, Etc

Funding Agency: Wellcome Trust

Related resources: Deciphering Developmental Disorders, Ensembl

References: PMID:19344873

Availability: Acknowledgement required

Website Status: Last checked up

Alternate IDs: nlx_151653, OMICS_00265

Abbreviations: DECIPHER

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