Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance

Author:

Yoon Christopher J.ORCID,Kim Su Yeon,Nam Chang Hyun,Lee Junehawk,Park Jung Woo,Mun Jihyeob,Park Seongyeol,Lee Soyoung,Yi Boram,Min Kyoung Il,Wiley Brian,Bolton Kelly L.,Lee Jeong Ho,Kim Eunjoon,Yoo Hee Jeong,Jun Jong Kwan,Choi Ji Seon,Griffith MalachiORCID,Griffith Obi L.ORCID,Ju Young SeokORCID

Abstract

With the increasing number of sequencing projects involving families, quality control tools optimized for family genome sequencing are needed. However, accurately quantifying contamination in a DNA mixture is particularly difficult when genetically related family members are the sources. We developed TrioMix, a maximum likelihood estimation (MLE) framework based on Mendel's law of inheritance, to quantify DNA mixture between family members in genome sequencing data of parent–offspring trios. TrioMix can accurately deconvolute any intrafamilial DNA contamination, including parent–offspring, sibling–sibling, parent–parent, and even multiple familial sources. In addition, TrioMix can be applied to detect genomic abnormalities that deviate from Mendelian inheritance patterns, such as uniparental disomy (UPD) and chimerism. A genome-wide depth and variant allele frequency plot generated by TrioMix facilitates tracing the origin of Mendelian inheritance deviations. We showed that TrioMix could accurately deconvolute genomes in both simulated and real data sets.

Funder

National Institutes of Health

National Research Foundation of Korea

Korean government, Ministry of Science and ICT

KREONET

Korea Institute of Science and Technology Information

Publisher

Cold Spring Harbor Laboratory

Subject

Genetics (clinical),Genetics

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