Multi-nucleotide de novo Mutations in Humans

Mutation of the DNA molecule is one of the most fundamental processes in biology. In this study, we use 283 parent-offspring trios to estimate the rate of mutation for both single nucleotide variants (SNVs) and short length variants (indels) in humans and examine the mutation process. We found 17812...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:PLoS Genet
Päätekijät: Besenbacher, Søren, Sulem, Patrick, Helgason, Agnar, Helgason, Hannes, Kristjansson, Helgi, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Magnusson, Olafur Th., Thorsteinsdottir, Unnur, Masson, Gisli, Kong, Augustine, Gudbjartsson, Daniel F., Stefansson, Kari
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2016
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5147774/
https://ncbi.nlm.nih.gov/pubmed/27846220
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006315
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