PRIMUS: Rapid Reconstruction of Pedigrees from Genome-wide Estimates of Identity by Descent
Understanding and correctly utilizing relatedness among samples is essential for genetic analysis; however, managing sample records and pedigrees can often be error prone and incomplete. Data sets ascertained by random sampling often harbor cryptic relatedness that can be leveraged in genetic analys...
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Veröffentlicht in: | American journal of human genetics 2014-11, Vol.95 (5), p.553-564 |
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creator | Staples, Jeffrey Qiao, Dandi Cho, Michael H. Silverman, Edwin K. Nickerson, Deborah A. Below, Jennifer E. |
description | Understanding and correctly utilizing relatedness among samples is essential for genetic analysis; however, managing sample records and pedigrees can often be error prone and incomplete. Data sets ascertained by random sampling often harbor cryptic relatedness that can be leveraged in genetic analyses for maximizing power. We have developed a method that uses genome-wide estimates of pairwise identity by descent to identify families and quickly reconstruct and score all possible pedigrees that fit the genetic data by using up to third-degree relatives, and we have included it in the software package PRIMUS (Pedigree Reconstruction and Identification of the Maximally Unrelated Set). Here, we validate its performance on simulated, clinical, and HapMap pedigrees. Among these samples, we demonstrate that PRIMUS can verify reported pedigree structures and identify cryptic relationships. Finally, we show that PRIMUS reconstructed pedigrees, all of which were previously unknown, for 203 families from a cohort collected in Starr County, TX (1,890 samples). |
doi_str_mv | 10.1016/j.ajhg.2014.10.005 |
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Data sets ascertained by random sampling often harbor cryptic relatedness that can be leveraged in genetic analyses for maximizing power. We have developed a method that uses genome-wide estimates of pairwise identity by descent to identify families and quickly reconstruct and score all possible pedigrees that fit the genetic data by using up to third-degree relatives, and we have included it in the software package PRIMUS (Pedigree Reconstruction and Identification of the Maximally Unrelated Set). Here, we validate its performance on simulated, clinical, and HapMap pedigrees. Among these samples, we demonstrate that PRIMUS can verify reported pedigree structures and identify cryptic relationships. Finally, we show that PRIMUS reconstructed pedigrees, all of which were previously unknown, for 203 families from a cohort collected in Starr County, TX (1,890 samples).</description><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>DOI: 10.1016/j.ajhg.2014.10.005</identifier><identifier>PMID: 25439724</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Base Sequence ; Computer Simulation ; Exome - genetics ; Families & family life ; Gene Frequency ; Genetics, Population - methods ; Genomics ; Humans ; Molecular Sequence Data ; Pedigree ; Pulmonary Disease, Chronic Obstructive - genetics ; Sequence Analysis, DNA ; Simulation ; Software ; Texas</subject><ispartof>American journal of human genetics, 2014-11, Vol.95 (5), p.553-564</ispartof><rights>2014 The American Society of Human Genetics</rights><rights>Copyright © 2014 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.</rights><rights>Copyright Cell Press Nov 6, 2014</rights><rights>2014 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2014 The American Society of Human Genetics</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c582t-eec05148e406691678cea17aa2c2ff5a44039ca4130df566311db1f82cb089543</citedby><cites>FETCH-LOGICAL-c582t-eec05148e406691678cea17aa2c2ff5a44039ca4130df566311db1f82cb089543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225580/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ajhg.2014.10.005$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3550,27924,27925,45995,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25439724$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Staples, Jeffrey</creatorcontrib><creatorcontrib>Qiao, Dandi</creatorcontrib><creatorcontrib>Cho, Michael H.</creatorcontrib><creatorcontrib>Silverman, Edwin K.</creatorcontrib><creatorcontrib>Nickerson, Deborah A.</creatorcontrib><creatorcontrib>Below, Jennifer E.</creatorcontrib><creatorcontrib>University of Washington Center for Mendelian Genomics</creatorcontrib><title>PRIMUS: Rapid Reconstruction of Pedigrees from Genome-wide Estimates of Identity by Descent</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><description>Understanding and correctly utilizing relatedness among samples is essential for genetic analysis; however, managing sample records and pedigrees can often be error prone and incomplete. Data sets ascertained by random sampling often harbor cryptic relatedness that can be leveraged in genetic analyses for maximizing power. We have developed a method that uses genome-wide estimates of pairwise identity by descent to identify families and quickly reconstruct and score all possible pedigrees that fit the genetic data by using up to third-degree relatives, and we have included it in the software package PRIMUS (Pedigree Reconstruction and Identification of the Maximally Unrelated Set). Here, we validate its performance on simulated, clinical, and HapMap pedigrees. Among these samples, we demonstrate that PRIMUS can verify reported pedigree structures and identify cryptic relationships. Finally, we show that PRIMUS reconstructed pedigrees, all of which were previously unknown, for 203 families from a cohort collected in Starr County, TX (1,890 samples).</description><subject>Base Sequence</subject><subject>Computer Simulation</subject><subject>Exome - genetics</subject><subject>Families & family life</subject><subject>Gene Frequency</subject><subject>Genetics, Population - methods</subject><subject>Genomics</subject><subject>Humans</subject><subject>Molecular Sequence Data</subject><subject>Pedigree</subject><subject>Pulmonary Disease, Chronic Obstructive - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>Simulation</subject><subject>Software</subject><subject>Texas</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EosvCH-CAInHhkmX8mQShSqiUdqUiqoWeOFheZ7J1tIkXOynaf4-jbauWA5wszzzz9b6EvKawoEDV-3Zh2uvNggEVKbAAkE_IjEpe5EqBfEpmAMDyilXFEXkRYwtAaQn8OTliUvCqYGJGfl6ull-vvn_IVmbn6myF1vdxCKMdnO8z32SXWLtNQIxZE3yXnWHvO8x_uxqz0zi4zgwplbhljf3ghn223mefMdr0e0meNWYb8dXtOydXX05_nJznF9_OliefLnIrSzbkiBYkFSUKUKqiqigtGloYwyxrGmmEAF5ZIyiHupFKcUrrNW1KZtdQVumSOTk-9N2N6w7raXQwW70Labuw1944_TjTu2u98TdaMCZlUmRO3t02CP7XiHHQnUsXbLemRz9GTRWXSXBIK_wfZVVVcMlkQt_-hbZ-DH1SYqJKJgQvi0SxA2WDjzFgc783BT3ZrFs92awnm6dYsjkVvXl48X3Jna8J-HgAMOl-4zDoaB32NpkZ0A669u5f_f8AJyO3yw</recordid><startdate>20141106</startdate><enddate>20141106</enddate><creator>Staples, Jeffrey</creator><creator>Qiao, Dandi</creator><creator>Cho, Michael H.</creator><creator>Silverman, Edwin K.</creator><creator>Nickerson, Deborah A.</creator><creator>Below, Jennifer E.</creator><general>Elsevier Inc</general><general>Cell Press</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20141106</creationdate><title>PRIMUS: Rapid Reconstruction of Pedigrees from Genome-wide Estimates of Identity by Descent</title><author>Staples, Jeffrey ; Qiao, Dandi ; Cho, Michael H. ; Silverman, Edwin K. ; Nickerson, Deborah A. ; Below, Jennifer E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c582t-eec05148e406691678cea17aa2c2ff5a44039ca4130df566311db1f82cb089543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Base Sequence</topic><topic>Computer Simulation</topic><topic>Exome - genetics</topic><topic>Families & family life</topic><topic>Gene Frequency</topic><topic>Genetics, Population - methods</topic><topic>Genomics</topic><topic>Humans</topic><topic>Molecular Sequence Data</topic><topic>Pedigree</topic><topic>Pulmonary Disease, Chronic Obstructive - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>Simulation</topic><topic>Software</topic><topic>Texas</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Staples, Jeffrey</creatorcontrib><creatorcontrib>Qiao, Dandi</creatorcontrib><creatorcontrib>Cho, Michael H.</creatorcontrib><creatorcontrib>Silverman, Edwin K.</creatorcontrib><creatorcontrib>Nickerson, Deborah A.</creatorcontrib><creatorcontrib>Below, Jennifer E.</creatorcontrib><creatorcontrib>University of Washington Center for Mendelian Genomics</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Staples, Jeffrey</au><au>Qiao, Dandi</au><au>Cho, Michael H.</au><au>Silverman, Edwin K.</au><au>Nickerson, Deborah A.</au><au>Below, Jennifer E.</au><aucorp>University of Washington Center for Mendelian Genomics</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PRIMUS: Rapid Reconstruction of Pedigrees from Genome-wide Estimates of Identity by Descent</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>2014-11-06</date><risdate>2014</risdate><volume>95</volume><issue>5</issue><spage>553</spage><epage>564</epage><pages>553-564</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><abstract>Understanding and correctly utilizing relatedness among samples is essential for genetic analysis; however, managing sample records and pedigrees can often be error prone and incomplete. Data sets ascertained by random sampling often harbor cryptic relatedness that can be leveraged in genetic analyses for maximizing power. We have developed a method that uses genome-wide estimates of pairwise identity by descent to identify families and quickly reconstruct and score all possible pedigrees that fit the genetic data by using up to third-degree relatives, and we have included it in the software package PRIMUS (Pedigree Reconstruction and Identification of the Maximally Unrelated Set). Here, we validate its performance on simulated, clinical, and HapMap pedigrees. Among these samples, we demonstrate that PRIMUS can verify reported pedigree structures and identify cryptic relationships. Finally, we show that PRIMUS reconstructed pedigrees, all of which were previously unknown, for 203 families from a cohort collected in Starr County, TX (1,890 samples).</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25439724</pmid><doi>10.1016/j.ajhg.2014.10.005</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence Computer Simulation Exome - genetics Families & family life Gene Frequency Genetics, Population - methods Genomics Humans Molecular Sequence Data Pedigree Pulmonary Disease, Chronic Obstructive - genetics Sequence Analysis, DNA Simulation Software Texas |
title | PRIMUS: Rapid Reconstruction of Pedigrees from Genome-wide Estimates of Identity by Descent |
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