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

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Title
Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance
Author(s)
Yoon, C.J.; Kim, S.Y.; Nam, C.H.; Lee, J.; Park, J.W.; Mun, J.; Park, S.; Lee, S.; Yi, B.; Min, K.I.; Wiley, B.; Bolton, K.L.; Lee, J.H.; Eunjoon Kim; Yoo, H.J.; Jun, J.K.; Choi, J.S.; Griffith, M.; Griffith, O.L.; Ju, Y.S.
Publication Date
2022-11
Journal
Genome Research, v.32, no.11-12, pp.2134 - 2144
Publisher
Cold Spring Harbor Laboratory Press
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. © 2022 Yoon et al.; Published by Cold Spring Harbor Laboratory Press.
URI
https://pr.ibs.re.kr/handle/8788114/12465
DOI
10.1101/gr.276794.122
ISSN
1088-9051
Appears in Collections:
Center for Synaptic Brain Dysfunctions(시냅스 뇌질환 연구단) > 1. Journal Papers (저널논문)
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