Challenges in medical applications of whole exome/genome sequencing discoveries (Q26824047)

main subject

whole genome sequencing

1 reference

Ali J. Marian

1

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Crossref

language of work or name

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November 2012

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Trends in Cardiovascular Medicine

published in

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volume

22

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issue

8

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page(s)

219-23

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The diploid genome sequence of an Asian individual

cites work

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Genetic variation in an individual human exome

7 April 2017

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Mapping and sequencing of structural variation from eight human genomes

7 April 2017

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The complete genome of an individual by massively parallel DNA sequencing

7 April 2017

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Paired-end mapping reveals extensive structural variation in the human genome

7 April 2017

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The diploid genome sequence of an individual human

7 April 2017

1 reference

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Initial sequencing and analysis of the human genome

7 April 2017

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

7 April 2017

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

7 April 2017

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Exome sequencing and the genetic basis of complex traits

7 April 2017

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The predictive capacity of personal genome sequencing

28 September 2017

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Elements of 'missing heritability'.

28 September 2017

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Truncations of titin causing dilated cardiomyopathy.

28 September 2017

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Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy

28 September 2017

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Strategic approaches to unraveling genetic causes of cardiovascular diseases

28 September 2017

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Recent explosive human population growth has resulted in an excess of rare genetic variants

28 September 2017

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Nature's genetic gradients and the clinical phenotype

31 May 2018

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An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

31 May 2018

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Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies.

28 November 2018

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Genomics. 1000 Genomes Project gives new map of genetic diversity

28 November 2018

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