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Human Knockout Carriers: Dead, Diseased, Healthy, or Improved?

Whole-genome and whole-exome sequence data from large numbers of individuals reveal that we all carry many variants predicted to inactivate genes (knockouts). This discovery raises questions about the phenotypic consequences of these knockouts and potentially allows us to study human gene function t...

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Detalles Bibliográficos
Autores principales: Narasimhan, Vagheesh M., Xue, Yali, Tyler-Smith, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826344/
https://www.ncbi.nlm.nih.gov/pubmed/26988438
http://dx.doi.org/10.1016/j.molmed.2016.02.006
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author Narasimhan, Vagheesh M.
Xue, Yali
Tyler-Smith, Chris
author_facet Narasimhan, Vagheesh M.
Xue, Yali
Tyler-Smith, Chris
author_sort Narasimhan, Vagheesh M.
collection PubMed
description Whole-genome and whole-exome sequence data from large numbers of individuals reveal that we all carry many variants predicted to inactivate genes (knockouts). This discovery raises questions about the phenotypic consequences of these knockouts and potentially allows us to study human gene function through the investigation of homozygous loss-of-function carriers. Here, we discuss strategies, recent results, and future prospects for large-scale human knockout studies. We examine their relevance to studying gene function, population genetics, and importantly, the implications for accurate clinical interpretations.
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spelling pubmed-48263442016-04-19 Human Knockout Carriers: Dead, Diseased, Healthy, or Improved? Narasimhan, Vagheesh M. Xue, Yali Tyler-Smith, Chris Trends Mol Med Review Whole-genome and whole-exome sequence data from large numbers of individuals reveal that we all carry many variants predicted to inactivate genes (knockouts). This discovery raises questions about the phenotypic consequences of these knockouts and potentially allows us to study human gene function through the investigation of homozygous loss-of-function carriers. Here, we discuss strategies, recent results, and future prospects for large-scale human knockout studies. We examine their relevance to studying gene function, population genetics, and importantly, the implications for accurate clinical interpretations. Elsevier Science Ltd 2016-04 /pmc/articles/PMC4826344/ /pubmed/26988438 http://dx.doi.org/10.1016/j.molmed.2016.02.006 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Narasimhan, Vagheesh M.
Xue, Yali
Tyler-Smith, Chris
Human Knockout Carriers: Dead, Diseased, Healthy, or Improved?
title Human Knockout Carriers: Dead, Diseased, Healthy, or Improved?
title_full Human Knockout Carriers: Dead, Diseased, Healthy, or Improved?
title_fullStr Human Knockout Carriers: Dead, Diseased, Healthy, or Improved?
title_full_unstemmed Human Knockout Carriers: Dead, Diseased, Healthy, or Improved?
title_short Human Knockout Carriers: Dead, Diseased, Healthy, or Improved?
title_sort human knockout carriers: dead, diseased, healthy, or improved?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826344/
https://www.ncbi.nlm.nih.gov/pubmed/26988438
http://dx.doi.org/10.1016/j.molmed.2016.02.006
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