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Best practices for the interpretation and reporting of clinical whole genome sequencing
by
Rehman, Atteeq U
, Belmont, John W
, Boczek Nicole
, Venner, Eric
, Kulkarni Shashikant
, Rehm, Heidi L
, Ellsworth, Katarzyna A
, Marcou Cherisse
, Barnett, Sarah
, Thomas-Wilson, Amanda
, Young, Ted
, Guha Saurav
, Jobanputra Vaidehi
, Austin-Tse, Christina A
, Perry, Denise L
, Bick, David
, Gibbs, Richard A
, Meng Linyan
, Kearney, Hutton M
, Chowdhury Shimul
, Taft, Ryan J
, Spiteri, Elizabeth
, Murdock, David R
in
Genetic disorders
/ Genomes
/ Health care
/ Whole genome sequencing
2022
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Best practices for the interpretation and reporting of clinical whole genome sequencing
by
Rehman, Atteeq U
, Belmont, John W
, Boczek Nicole
, Venner, Eric
, Kulkarni Shashikant
, Rehm, Heidi L
, Ellsworth, Katarzyna A
, Marcou Cherisse
, Barnett, Sarah
, Thomas-Wilson, Amanda
, Young, Ted
, Guha Saurav
, Jobanputra Vaidehi
, Austin-Tse, Christina A
, Perry, Denise L
, Bick, David
, Gibbs, Richard A
, Meng Linyan
, Kearney, Hutton M
, Chowdhury Shimul
, Taft, Ryan J
, Spiteri, Elizabeth
, Murdock, David R
in
Genetic disorders
/ Genomes
/ Health care
/ Whole genome sequencing
2022
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Do you wish to request the book?
Best practices for the interpretation and reporting of clinical whole genome sequencing
by
Rehman, Atteeq U
, Belmont, John W
, Boczek Nicole
, Venner, Eric
, Kulkarni Shashikant
, Rehm, Heidi L
, Ellsworth, Katarzyna A
, Marcou Cherisse
, Barnett, Sarah
, Thomas-Wilson, Amanda
, Young, Ted
, Guha Saurav
, Jobanputra Vaidehi
, Austin-Tse, Christina A
, Perry, Denise L
, Bick, David
, Gibbs, Richard A
, Meng Linyan
, Kearney, Hutton M
, Chowdhury Shimul
, Taft, Ryan J
, Spiteri, Elizabeth
, Murdock, David R
in
Genetic disorders
/ Genomes
/ Health care
/ Whole genome sequencing
2022
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Best practices for the interpretation and reporting of clinical whole genome sequencing
Journal Article
Best practices for the interpretation and reporting of clinical whole genome sequencing
2022
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Overview
Whole genome sequencing (WGS) shows promise as a first-tier diagnostic test for patients with rare genetic disorders. However, standards addressing the definition and deployment practice of a best-in-class test are lacking. To address these gaps, the Medical Genome Initiative, a consortium of leading health care and research organizations in the US and Canada, was formed to expand access to high quality clinical WGS by convening experts and publishing best practices. Here, we present best practice recommendations for the interpretation and reporting of clinical diagnostic WGS, including discussion of challenges and emerging approaches that will be critical to harness the full potential of this comprehensive test.
Publisher
Nature Publishing Group
Subject
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