Whole genome sequencing: a considered approach to clinical implementation (Q56773312)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23595600%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

title

Whole genome sequencing: a considered approach to clinical implementation (English)

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28 February 2020

main subject

whole genome sequencing

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1

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author name string

David Dimmock

series ordinal

1

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language of work or name

English

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publication date

1 January 2013

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23595600%20AND%20SRC:MED&resulttype=core&format=json

Current protocols in human genetics / editorial board, Nicholas C, Dracapoli ... [et al.]

28 February 2020

published in

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28 February 2020

volume

Chapter 9

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page(s)

Unit9.22

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Accurate and comprehensive sequencing of personal genomes

28 February 2020

cites work

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https://api.crossref.org/works/10.1002%2F0471142905.HG0922S77

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

21 January 2018

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Whole exome and whole genome sequencing

21 January 2018

1 reference

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Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project

21 January 2018

1 reference

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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

21 January 2018

1 reference

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The legal risks of returning results of genomics research

21 January 2018

1 reference

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A personal perspective on returning secondary results of clinical genome sequencing

21 January 2018

1 reference

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Return of results: not that complicated?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0922S77

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0922S77

Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0922S77

Assuring the quality of next-generation sequencing in clinical laboratory practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0922S77

Next-generation sequencing facilitates the diagnosis in a child with twinkle mutations causing cholestatic liver failure.

21 January 2018

1 reference

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Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors

21 January 2018

1 reference

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Exploring concordance and discordance for return of incidental findings from clinical sequencing

21 January 2018

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21 January 2018

1 reference

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Taxonomizing, sizing, and overcoming the incidentalome

21 January 2018

1 reference

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A timely arrival for genomic medicine

21 January 2018

1 reference

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CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network

21 January 2018

1 reference

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

21 January 2018

1 reference

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10.1002/0471142905.HG0922S77

21 January 2018

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23595600%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

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