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Published Erratum
. 2021 Mar 9;118(10):e2102070118.
doi: 10.1073/pnas.2102070118.

Correction for Kessler et al., De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

No authors listed
Published Erratum

Correction for Kessler et al., De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

No authors listed. Proc Natl Acad Sci U S A. .
No abstract available

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Figures

Fig. 1.
Fig. 1.
Distribution of single-base and 3-mer mutation types across SNV DNM call set. (A) The distribution of single-base mutation type counts across our SNV DNM call set is shown. Colors represent mutation type, and stars represent associations with paternal age (red, P < 0.05 after Bonferroni correction). (B) The counts across our DNM call set for each of 96 3-mer mutation types is shown. Colors represent the center base mutation, and are the same as those in A. Stars represent associations with paternal age (red, P < 0.05 after Bonferroni correction).
See this image and copyright information in PMC

Erratum for

  • De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
    Kessler MD, Loesch DP, Perry JA, Heard-Costa NL, Taliun D, Cade BE, Wang H, Daya M, Ziniti J, Datta S, Celedón JC, Soto-Quiros ME, Avila L, Weiss ST, Barnes K, Redline SS, Vasan RS, Johnson AD, Mathias RA, Hernandez R, Wilson JG, Nickerson DA, Abecasis G, Browning SR, Zöllner S, O'Connell JR, Mitchell BD; National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium; TOPMed Population Genetics Working Group; O'Connor TD. Kessler MD, et al. Proc Natl Acad Sci U S A. 2020 Feb 4;117(5):2560-2569. doi: 10.1073/pnas.1902766117. Epub 2020 Jan 21. Proc Natl Acad Sci U S A. 2020. PMID: 31964835 Free PMC article.

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