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Selecting Clustering Algorithms for Identity-By-Descent Mapping
Groups of distantly related individuals who share a short segment of their genome identical-by-descent (IBD) can provide insights about rare traits and diseases in massive biobanks using IBD mapping. Clustering algorithms play an important role in finding these groups accurately and at scale. We set...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782725/ https://www.ncbi.nlm.nih.gov/pubmed/36540970 |
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author | Shemirani, Ruhollah Belbin, Gillian M Burghardt, Keith Lerman, Kristina Avery, Christy L Kenny, Eimear E Gignoux, Christopher R Ambite, José Luis |
author_facet | Shemirani, Ruhollah Belbin, Gillian M Burghardt, Keith Lerman, Kristina Avery, Christy L Kenny, Eimear E Gignoux, Christopher R Ambite, José Luis |
author_sort | Shemirani, Ruhollah |
collection | PubMed |
description | Groups of distantly related individuals who share a short segment of their genome identical-by-descent (IBD) can provide insights about rare traits and diseases in massive biobanks using IBD mapping. Clustering algorithms play an important role in finding these groups accurately and at scale. We set out to analyze the fitness of commonly used, fast and scalable clustering algorithms for IBD mapping applications. We designed a realistic benchmark for local IBD graphs and utilized it to compare the statistical power of clustering algorithms via simulating 2.3 million clusters across 850 experiments. We found Infomap and Markov Clustering (MCL) community detection methods to have high statistical power in most of the scenarios. They yield a 30% increase in power compared to the current state-of-art approach, with a 3 orders of magnitude lower runtime. We also found that standard clustering metrics, such as modularity, cannot predict statistical power of algorithms in IBD mapping applications. We extend our findings to real datasets by analyzing the Population Architecture using Genomics and Epidemiology (PAGE) Study dataset with 51,000 samples and 2 million shared segments on Chromosome 1, resulting in the extraction of 39 million local IBD clusters. We demonstrate the power of our approach by recovering signals of rare genetic variation in the Whole-Exome Sequence data of 200,000 individuals in the UK Biobank. We provide an efficient implementation to enable clustering at scale for IBD mapping for various populations and scenarios. |
format | Online Article Text |
id | pubmed-9782725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-97827252023-01-01 Selecting Clustering Algorithms for Identity-By-Descent Mapping Shemirani, Ruhollah Belbin, Gillian M Burghardt, Keith Lerman, Kristina Avery, Christy L Kenny, Eimear E Gignoux, Christopher R Ambite, José Luis Pac Symp Biocomput Article Groups of distantly related individuals who share a short segment of their genome identical-by-descent (IBD) can provide insights about rare traits and diseases in massive biobanks using IBD mapping. Clustering algorithms play an important role in finding these groups accurately and at scale. We set out to analyze the fitness of commonly used, fast and scalable clustering algorithms for IBD mapping applications. We designed a realistic benchmark for local IBD graphs and utilized it to compare the statistical power of clustering algorithms via simulating 2.3 million clusters across 850 experiments. We found Infomap and Markov Clustering (MCL) community detection methods to have high statistical power in most of the scenarios. They yield a 30% increase in power compared to the current state-of-art approach, with a 3 orders of magnitude lower runtime. We also found that standard clustering metrics, such as modularity, cannot predict statistical power of algorithms in IBD mapping applications. We extend our findings to real datasets by analyzing the Population Architecture using Genomics and Epidemiology (PAGE) Study dataset with 51,000 samples and 2 million shared segments on Chromosome 1, resulting in the extraction of 39 million local IBD clusters. We demonstrate the power of our approach by recovering signals of rare genetic variation in the Whole-Exome Sequence data of 200,000 individuals in the UK Biobank. We provide an efficient implementation to enable clustering at scale for IBD mapping for various populations and scenarios. 2023 /pmc/articles/PMC9782725/ /pubmed/36540970 Text en https://creativecommons.org/licenses/by-nc/4.0/Open Access chapter published by World Scientific Publishing Company and distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC) 4.0 License. |
spellingShingle | Article Shemirani, Ruhollah Belbin, Gillian M Burghardt, Keith Lerman, Kristina Avery, Christy L Kenny, Eimear E Gignoux, Christopher R Ambite, José Luis Selecting Clustering Algorithms for Identity-By-Descent Mapping |
title | Selecting Clustering Algorithms for Identity-By-Descent Mapping |
title_full | Selecting Clustering Algorithms for Identity-By-Descent Mapping |
title_fullStr | Selecting Clustering Algorithms for Identity-By-Descent Mapping |
title_full_unstemmed | Selecting Clustering Algorithms for Identity-By-Descent Mapping |
title_short | Selecting Clustering Algorithms for Identity-By-Descent Mapping |
title_sort | selecting clustering algorithms for identity-by-descent mapping |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782725/ https://www.ncbi.nlm.nih.gov/pubmed/36540970 |
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