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Updated: Nov 1, 2025

Characterizing Mutational Load and Clonal Composition of Human Blood
Published on: July 11, 2019
The origin of human mutation in light of genomic data
Vladimir B Seplyarskiy1,2, Shamil Sunyaev3,4
1Division of Genetics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Abstract:
Despite years of active research into the role of DNA repair and replication in mutagenesis, surprisingly little is known about the origin of spontaneous human mutation in the germ line. With the advent of high-throughput sequencing, genome-scale data have revealed statistical properties of mutagenesis in humans. These properties include variation of the mutation rate and spectrum along the genome at different scales in relation to epigenomic features and dependency on parental age. Moreover, mutations originated in mothers are less frequent than mutations originated in fathers and have a distinct genomic distribution. Statistical analyses that interpret these patterns in the context of known biochemistry can provide mechanistic models of mutagenesis in humans.
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