(Q57839685)

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Whole-Genome Sequencing: The New Standard of Care?

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title

Whole-Genome Sequencing: The New Standard of Care? (English)

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main subject

whole genome sequencing

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L. R. Brunham

1

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M. R. Hayden

series ordinal

2

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language of work or name

English

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publication date

31 May 2012

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number of pages

2

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published in

Science

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volume

336

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page(s)

1112-1113

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issue

6085

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Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

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The predictive capacity of personal genome sequencing

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The characterization of twenty sequenced human genomes

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A systematic survey of loss-of-function variants in human protein-coding genes

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A timely arrival for genomic medicine

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Bilateral prophylactic mastectomy reduces breast cancer risk in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group

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HLA-B*5701 screening for hypersensitivity to abacavir

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

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Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

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21 January 2018

Identifiers

DOI

10.1126/SCIENCE.1220967

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(Q57839685)

Whole-Genome Sequencing: The New Standard of Care?

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