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Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance
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 develope...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808622/ https://www.ncbi.nlm.nih.gov/pubmed/36617634 http://dx.doi.org/10.1101/gr.276794.122 |
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author | Yoon, Christopher J. 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, Malachi Griffith, Obi L. Ju, Young Seok |
author_facet | Yoon, Christopher J. 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, Malachi Griffith, Obi L. Ju, Young Seok |
author_sort | Yoon, Christopher J. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9808622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98086222023-01-20 Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance Yoon, Christopher J. 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, Malachi Griffith, Obi L. Ju, Young Seok Genome Res Method 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. Cold Spring Harbor Laboratory Press 2022 /pmc/articles/PMC9808622/ /pubmed/36617634 http://dx.doi.org/10.1101/gr.276794.122 Text en © 2022 Yoon et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Method Yoon, Christopher J. 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, Malachi Griffith, Obi L. Ju, Young Seok Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance |
title | Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance |
title_full | Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance |
title_fullStr | Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance |
title_full_unstemmed | Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance |
title_short | Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance |
title_sort | estimation of intrafamilial dna contamination in family trio genome sequencing using deviation from mendelian inheritance |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808622/ https://www.ncbi.nlm.nih.gov/pubmed/36617634 http://dx.doi.org/10.1101/gr.276794.122 |
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