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The Need for a Human Pangenome Reference Sequence.
Miga, Karen H; Wang, Ting.
Afiliação
  • Miga KH; UC Santa Cruz Genomics Institute and Department of Biomedical Engineering, University of California, Santa Cruz, California 95064, USA; email: khmiga@ucsc.edu.
  • Wang T; Department of Genetics, Edison Family Center for Genome Sciences and Systems Biology, and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri 63110, USA; email: twang@wustl.edu.
Annu Rev Genomics Hum Genet ; 22: 81-102, 2021 08 31.
Article em En | MEDLINE | ID: mdl-33929893
The reference human genome sequence is inarguably the most important and widely used resource in the fields of human genetics and genomics. It has transformed the conduct of biomedical sciences and brought invaluable benefits to the understanding and improvement of human health. However, the commonly used reference sequence has profound limitations, because across much of its span, it represents the sequence of just one human haplotype. This single, monoploid reference structure presents a critical barrier to representing the broad genomic diversity in the human population. In this review, we discuss the modernization of the reference human genome sequence to a more complete reference of human genomic diversity, known as a human pangenome.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Genômica Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Genômica Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article