z-logo
open-access-imgOpen Access
Genetic and epigenetic contribution to complex traits
Author(s) -
Helena Kilpinen,
Emmanouil T. Dermitzakis
Publication year - 2012
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/dds383
Subject(s) - biology , epigenome , epigenetics , genomics , genetics , computational biology , functional genomics , dna sequencing , genome , phenotype , human genetics , human genetic variation , human genome , genetic variation , population genomics , context (archaeology) , inheritance (genetic algorithm) , dna methylation , gene , gene expression , paleontology
Much of the recent advances in functional genomics owe to developments in next-generation sequencing technology, which has contributed to the exponential increase of genomic data available for different human disease and population samples. With functional sequencing assays available to query both the transcriptome and the epigenome, annotation of the non-coding, regulatory genome is steadily improving and providing means to interpret the functional consequences of genetic variants associated with human complex traits. This has highlighted the need to better understand the normal variation in various cellular phenotypes, such as epigenetic modifications, and their transgenerational inheritance. In this review, we discuss different aspects of epigenetic variation in the context of DNA sequence variation and its contribution to complex phenotypes.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom