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The human noncoding genome defined by genetic diversity.
di Iulio, Julia; Bartha, Istvan; Wong, Emily H M; Yu, Hung-Chun; Lavrenko, Victor; Yang, Dongchan; Jung, Inkyung; Hicks, Michael A; Shah, Naisha; Kirkness, Ewen F; Fabani, Martin M; Biggs, William H; Ren, Bing; Venter, J Craig; Telenti, Amalio.
Afiliação
  • di Iulio J; Human Longevity, Inc., San Diego, CA, USA.
  • Bartha I; Scripps Research Institute , La Jolla, CA, USA.
  • Wong EHM; Human Longevity, Inc., San Diego, CA, USA.
  • Yu HC; Swiss Federal Institute of Technology, Lausanne, Switzerland.
  • Lavrenko V; Human Longevity, Inc., San Diego, CA, USA.
  • Yang D; Human Longevity, Inc., San Diego, CA, USA.
  • Jung I; Human Longevity, Inc., San Diego, CA, USA.
  • Hicks MA; Department of Biological Science, Korea Advanced Institute of Science & Technology, Daejeon, Korea.
  • Shah N; Department of Biological Science, Korea Advanced Institute of Science & Technology, Daejeon, Korea.
  • Kirkness EF; Human Longevity, Inc., San Diego, CA, USA.
  • Fabani MM; Human Longevity, Inc., San Diego, CA, USA.
  • Biggs WH; Human Longevity, Inc., San Diego, CA, USA.
  • Ren B; Human Longevity, Inc., San Diego, CA, USA.
  • Venter JC; Verogen , San Diego, CA, USA.
  • Telenti A; Human Longevity, Inc., San Diego, CA, USA.
Nat Genet ; 50(3): 333-337, 2018 03.
Article em En | MEDLINE | ID: mdl-29483654
Understanding the significance of genetic variants in the noncoding genome is emerging as the next challenge in human genomics. We used the power of 11,257 whole-genome sequences and 16,384 heptamers (7-nt motifs) to build a map of sequence constraint for the human species. This build differed substantially from traditional maps of interspecies conservation and identified regulatory elements among the most constrained regions of the genome. Using new Hi-C experimental data, we describe a strong pattern of coordination over 2 Mb where the most constrained regulatory elements associate with the most essential genes. Constrained regions of the noncoding genome are up to 52-fold enriched for known pathogenic variants as compared to unconstrained regions (21-fold when compared to the genome average). This map of sequence constraint across thousands of individuals is an asset to help interpret noncoding elements in the human genome, prioritize variants and reconsider gene units at a larger scale.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Genoma Humano / RNA não Traduzido Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Genoma Humano / RNA não Traduzido Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos