Evidence map›Paper›PMID 36263419›Full record

ArticleFrontiers in genetics2022

A machine learning approach for missing persons cases with high genotyping errors.

Meng Huang, Muyi Liu, Hongmin Li, Jonathan King, Amy Smuts, Bruce Budowle, Jianye Ge

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Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Meng HuangCenter for Human Identification, University of North Texas Health Science Center, Fort Worth, TX, United States.
Muyi LiuCenter for Human Identification, University of North Texas Health Science Center, Fort Worth, TX, United States.
Hongmin LiDepartment of Computer Science, College of Science, California State University, East Bay, Hayward, CA, United States.
Jonathan KingCenter for Human Identification, University of North Texas Health Science Center, Fort Worth, TX, United States.
Amy SmutsCenter for Human Identification, University of North Texas Health Science Center, Fort Worth, TX, United States.
Bruce BudowleCenter for Human Identification, University of North Texas Health Science Center, Fort Worth, TX, United States.
Jianye GeCenter for Human Identification, University of North Texas Health Science Center, Fort Worth, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estimating the relationships between individuals is one of the fundamental challenges in many fields. In particular, relationship.ip estimation could provide valuable information for missing persons cases. The recently developed investigative genetic genealogy approach uses high-density single nucleotide polymorphisms (SNPs) to determine close and more distant relationships, in which hundreds of thousands to tens of millions of SNPs are generated either by microarray genotyping or whole-genome sequencing. The current studies usually assume the SNP profiles were generated with minimum errors. However, in the missing person cases, the DNA samples can be highly degraded, and the SNP profiles generated from these samples usually contain lots of errors. In this study, a machine learning approach was developed for estimating the relationships with high error SNP profiles. In this approach, a hierarchical classification strategy was employed first to classify the relationships by degree and then the relationship types within each degree separately. As for each classification, feature selection was implemented to gain better performance. Both simulated and real data sets with various genotyping error rates were utilized in evaluating this approach, and the accuracies of this approach were higher than individual measures; namely, this approach was more accurate and robust than the individual measures for SNP profiles with genotyping errors. In addition, the highest accuracy could be obtained by providing the same genotyping error rates in train and test sets, and thus estimating genotyping errors of the SNP profiles is critical to obtaining high accuracy of relationship estimation.

Indexed as

feature selectiongenetic genealogygenotyping errorhierarchical classificationkinship estimationmachine learningmissing personsingle nucleotide polymorphisms

Identifiers

PMID36263419
PMCPMC9573995

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.