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dc.contributor.authorBedoya Berrío, Gabriel de Jesús-
dc.contributor.authorLin, Chia-Ho-
dc.contributor.authorService, Susan-
dc.contributor.authorChen, Yuguo-
dc.contributor.authorFreimer, Nelson-
dc.contributor.authorSabatti, Chiara-
dc.contributor.authorWang, Hui-
dc.contributor.authorOspina Duque, Jorge-
dc.date.accessioned2024-08-28T01:01:59Z-
dc.date.available2024-08-28T01:01:59Z-
dc.date.issued2006-
dc.identifier.issn0001-5652-
dc.identifier.urihttps://hdl.handle.net/10495/41530-
dc.description.abstractABSTRACT: Objective: Analyze the information contained in homozygous haplotypes detected with high density genotyping. Methods: We analyze the genotypes of ∼2,500 markers on chr 22 in 12 population samples, each including 200 individuals. We develop a measure of disequilibrium based on haplotype homozygosity and an algorithm to identify genomic segments characterized by non-random homozygosity (NRH), taking into account allele frequencies, missing data, genotyping error, and linkage disequilibrium. Results: We show how our measure of linkage disequilibrium based on homozygosity leads to results comparable to those of R2, as well as the importance of correcting for small sample variation when evaluating D′. We observe that the regions that harbor NRH segments tend to be consistent across populations, are gene rich, and are characterized by lower recombination. Conclusions: It is crucial to take into account LD patterns when interpreting long stretches of homozygous markers.spa
dc.format.extent15 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherKargerspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc/2.5/co/*
dc.titleLinkage Disequilibrium and Haplotype Homozygosity in Population Samples Genotyped at a High Marker Densityspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGenética Molecular (GENMOL)spa
dc.publisher.groupGrupo de Investigación en Psiquiatría GIPSIspa
dc.identifier.doi10.1159/000096599-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1423-0062-
oaire.citationtitleHuman Heredityspa
oaire.citationstartpage175spa
oaire.citationendpage189spa
oaire.citationvolume62spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc/4.0/spa
dc.publisher.placeBasilea, Suizaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsConsanguinidad-
dc.subject.decsConsanguinity-
dc.subject.decsCromosomas Humanos Par 22-
dc.subject.decsChromosomes, Human, Pair 22-
dc.subject.decsFrecuencia de los Genes-
dc.subject.decsGene Frequency-
dc.subject.decsMarcadores Genéticos-
dc.subject.decsGenetic Markers-
dc.subject.decsCadenas de Markov-
dc.subject.decsMarkov Chains-
dc.subject.decsHomocigoto-
dc.subject.decsHomozygote-
dc.description.researchgroupidCOL0006723spa
dc.description.researchgroupidCOL0029147spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D003241-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D002892-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D005787-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D005819-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D008390-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D006720-
dc.relation.ispartofjournalabbrevHum. Hered.spa
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