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Perspectives on Allele-Specific Expression.
Cleary, Siobhan; Seoighe, Cathal.
Afiliação
  • Cleary S; School of Mathematics, Statistics and Applied Mathematics, National University of Ireland, Galway H91 H3CY, Ireland; email: cathal.seoighe@nuigalway.ie.
  • Seoighe C; School of Mathematics, Statistics and Applied Mathematics, National University of Ireland, Galway H91 H3CY, Ireland; email: cathal.seoighe@nuigalway.ie.
Annu Rev Biomed Data Sci ; 4: 101-122, 2021 07 20.
Article em En | MEDLINE | ID: mdl-34465174
ABSTRACT
Diploidy has profound implications for population genetics and susceptibility to genetic diseases. Although two copies are present for most genes in the human genome, they are not necessarily both active or active at the same level in a given individual. Genomic imprinting, resulting in exclusive or biased expression in favor of the allele of paternal or maternal origin, is now believed to affect hundreds of human genes. A far greater number of genes display unequal expression of gene copies due to cis-acting genetic variants that perturb gene expression. The availability of data generated by RNA sequencing applied to large numbers of individuals and tissue types has generated unprecedented opportunities to assess the contribution of genetic variation to allelic imbalance in gene expression. Here we review the insights gained through the analysis of these data about the extent of the genetic contribution to allelic expression imbalance, the tools and statistical models for gene expression imbalance, and what the results obtained reveal about the contribution of genetic variants that alter gene expression to complex human diseases and phenotypes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Impressão Genômica / Desequilíbrio Alélico Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Annu Rev Biomed Data Sci Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Impressão Genômica / Desequilíbrio Alélico Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Annu Rev Biomed Data Sci Ano de publicação: 2021 Tipo de documento: Article