Genetic analysis of complex diseases
The probability that a heterozygous Bb subject carries A in coupling when B is alpha sub(1) = p + delta /m, and the probability that the same subject carries A in coupling with b is alpha sub(2) = p - delta (1 - m). In a sample of single affected individuals for a Bb parent to transmit B to his affe...
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Veröffentlicht in: | Science (American Association for the Advancement of Science) 1997-02, Vol.275 (5304), p.1328; author reply 1329-1329 |
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creator | Long, A D Grote, M N Langley, C H |
description | The probability that a heterozygous Bb subject carries A in coupling when B is alpha sub(1) = p + delta /m, and the probability that the same subject carries A in coupling with b is alpha sub(2) = p - delta (1 - m). In a sample of single affected individuals for a Bb parent to transmit B to his affected child is P(tr - B) = [1 + ( gamma - 1) alpha sub(1)]/[2 + ( gamma - 1)( alpha sub(1) + alpha sub(2))]. The situation described by Risch and Merikangas corresponds to complete linkage disequilibrium, that is, delta = delta sub(max) with m = p, with P(tr - B) reducing to gamma /(1 + gamma ). In other cases, the number of necessary families increases dramatically as p differs from m even when delta = delta sub(max), and also as delta decreases. Thus, the power of association studies such as the TDT can be quite strong when there is a high probability that the allele studied is the causal allele as shown by Risch and Merikangas. In other cases, researchers should be aware that the power of such association studies can be greatly diminished as soon as the ratio m/p departs from unity and the linkage disequilibrium becomes weaker. |
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In a sample of single affected individuals for a Bb parent to transmit B to his affected child is P(tr - B) = [1 + ( gamma - 1) alpha sub(1)]/[2 + ( gamma - 1)( alpha sub(1) + alpha sub(2))]. The situation described by Risch and Merikangas corresponds to complete linkage disequilibrium, that is, delta = delta sub(max) with m = p, with P(tr - B) reducing to gamma /(1 + gamma ). In other cases, the number of necessary families increases dramatically as p differs from m even when delta = delta sub(max), and also as delta decreases. Thus, the power of association studies such as the TDT can be quite strong when there is a high probability that the allele studied is the causal allele as shown by Risch and Merikangas. In other cases, researchers should be aware that the power of such association studies can be greatly diminished as soon as the ratio m/p departs from unity and the linkage disequilibrium becomes weaker.</description><identifier>ISSN: 0036-8075</identifier><identifier>PMID: 9064790</identifier><language>eng</language><publisher>United States</publisher><subject>Alleles ; Chromosome Mapping ; Genetic Diseases, Inborn - genetics ; Genetic Markers ; Genetic Predisposition to Disease ; Genetics, Population ; Genotype ; Humans ; Polymorphism, Genetic ; Prospective Studies ; Sampling Studies</subject><ispartof>Science (American Association for the Advancement of Science), 1997-02, Vol.275 (5304), p.1328; author reply 1329-1329</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9064790$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Long, A D</creatorcontrib><creatorcontrib>Grote, M N</creatorcontrib><creatorcontrib>Langley, C H</creatorcontrib><title>Genetic analysis of complex diseases</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>The probability that a heterozygous Bb subject carries A in coupling when B is alpha sub(1) = p + delta /m, and the probability that the same subject carries A in coupling with b is alpha sub(2) = p - delta (1 - m). In a sample of single affected individuals for a Bb parent to transmit B to his affected child is P(tr - B) = [1 + ( gamma - 1) alpha sub(1)]/[2 + ( gamma - 1)( alpha sub(1) + alpha sub(2))]. The situation described by Risch and Merikangas corresponds to complete linkage disequilibrium, that is, delta = delta sub(max) with m = p, with P(tr - B) reducing to gamma /(1 + gamma ). In other cases, the number of necessary families increases dramatically as p differs from m even when delta = delta sub(max), and also as delta decreases. Thus, the power of association studies such as the TDT can be quite strong when there is a high probability that the allele studied is the causal allele as shown by Risch and Merikangas. In other cases, researchers should be aware that the power of such association studies can be greatly diminished as soon as the ratio m/p departs from unity and the linkage disequilibrium becomes weaker.</description><subject>Alleles</subject><subject>Chromosome Mapping</subject><subject>Genetic Diseases, Inborn - genetics</subject><subject>Genetic Markers</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetics, Population</subject><subject>Genotype</subject><subject>Humans</subject><subject>Polymorphism, Genetic</subject><subject>Prospective Studies</subject><subject>Sampling Studies</subject><issn>0036-8075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0EtLAzEUBeAslFprf4IwC3E3kDTvpRSthYIbXQ-Z5AZSMg_nzoD99w44e7u6m--cA_eGrCnlqjRUyztyj3imlFpp-YqsLFVCW7omTwdoYUy-cK3LF0xYdLHwXdNn-ClCQnAI-EBuo8sI2-VuyNfb6-f-vTx9HI77l1PZc6XHUjoAr6zytY_SWwFSRsc5Y8YJGiRobaJhNoKwog5BKhu0MCB0rXZUcc835Pmvtx-67wlwrJqEHnJ2LXQTVtoYNaf0VXAeNv9CJg2X4jq4s5qJGT4ucKobCFU_pMYNl2r5KP8FmWFvOA</recordid><startdate>19970228</startdate><enddate>19970228</enddate><creator>Long, A D</creator><creator>Grote, M N</creator><creator>Langley, C H</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19970228</creationdate><title>Genetic analysis of complex diseases</title><author>Long, A D ; Grote, M N ; Langley, C H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p367t-5aeec696cbcf5c94e55fa33118a40d5e778f819fe494bdd569d748e47b62063c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Alleles</topic><topic>Chromosome Mapping</topic><topic>Genetic Diseases, Inborn - genetics</topic><topic>Genetic Markers</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetics, Population</topic><topic>Genotype</topic><topic>Humans</topic><topic>Polymorphism, Genetic</topic><topic>Prospective Studies</topic><topic>Sampling Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Long, A D</creatorcontrib><creatorcontrib>Grote, M N</creatorcontrib><creatorcontrib>Langley, C H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Long, A D</au><au>Grote, M N</au><au>Langley, C H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic analysis of complex diseases</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>1997-02-28</date><risdate>1997</risdate><volume>275</volume><issue>5304</issue><spage>1328; author reply 1329</spage><epage>1329</epage><pages>1328; author reply 1329-1329</pages><issn>0036-8075</issn><abstract>The probability that a heterozygous Bb subject carries A in coupling when B is alpha sub(1) = p + delta /m, and the probability that the same subject carries A in coupling with b is alpha sub(2) = p - delta (1 - m). In a sample of single affected individuals for a Bb parent to transmit B to his affected child is P(tr - B) = [1 + ( gamma - 1) alpha sub(1)]/[2 + ( gamma - 1)( alpha sub(1) + alpha sub(2))]. The situation described by Risch and Merikangas corresponds to complete linkage disequilibrium, that is, delta = delta sub(max) with m = p, with P(tr - B) reducing to gamma /(1 + gamma ). In other cases, the number of necessary families increases dramatically as p differs from m even when delta = delta sub(max), and also as delta decreases. Thus, the power of association studies such as the TDT can be quite strong when there is a high probability that the allele studied is the causal allele as shown by Risch and Merikangas. In other cases, researchers should be aware that the power of such association studies can be greatly diminished as soon as the ratio m/p departs from unity and the linkage disequilibrium becomes weaker.</abstract><cop>United States</cop><pmid>9064790</pmid><tpages>2</tpages></addata></record> |
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language | eng |
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source | MEDLINE; JSTOR Archive Collection A-Z Listing; American Association for the Advancement of Science |
subjects | Alleles Chromosome Mapping Genetic Diseases, Inborn - genetics Genetic Markers Genetic Predisposition to Disease Genetics, Population Genotype Humans Polymorphism, Genetic Prospective Studies Sampling Studies |
title | Genetic analysis of complex diseases |
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