Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.
about
Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigreesDetection of identity by descent using next-generation whole genome sequencing dataFinding the missing heritability of complex diseasesThe role of large pedigrees in an era of high-throughput sequencingA system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.HapFABIA: identification of very short segments of identity by descent characterized by rare variants in large sequencing data.Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.Assessment of SNP streak statistics using gene drop simulation with linkage disequilibrium.Improved IBD detection using incomplete haplotype information.High-resolution detection of identity by descent in unrelated individualsQuality control issues and the identification of rare functional variants with next-generation sequencing data.A fast, powerful method for detecting identity by descent.Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics.Detecting rare variant associations by identity-by-descent mapping in case-control studies.IBD-Groupon: an efficient method for detecting group-wise identity-by-descent regions simultaneously in multiple individuals based on pairwise IBD relationships.Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees.Maximum-likelihood estimation of recent shared ancestry (ERSA).Whole population, genome-wide mapping of hidden relatednessA genome scan conducted in a multigenerational pedigree with convergent strabismus supports a complex genetic determinismCombinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.Estimation and visualization of identity-by-descent within pedigrees simplifies interpretation of complex trait analysis.FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease StudiesPedigree-Free Descent-Based Gene Mapping from Population SamplesLinkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort.Identity by descent: variation in meiosis, across genomes, and in populationsOptimized selection of unrelated subjects for whole-genome sequencing studies of rare high-penetrance alleles.A population-based analysis of clustering identifies a strong genetic contribution to lethal prostate cancerEstimation of graphical models whose conditional independence graphs are interval graphs and its application to modeling linkage disequilibrium.A method and program for estimating graphical models for linkage disequilibrium that scale linearly with the number of loci, and their application to gene drop simulationReplication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based studyShared genomic segment analysis: the power to find rare disease variantsIdentifying bipolar disorder susceptibility loci in a densely affected pedigree.IBD Sharing between Africans, Neandertals, and Denisovans.Family-based studies to identify genetic variants that cause congenital heart defects.A Genealogical Look at Shared Ancestry on the X Chromosome.HaploShare: identification of extended haplotypes shared by cases and evaluation against controlsIdentification of regions of positive selection using Shared Genomic Segment analysis.Accuracy and computational efficiency of a graphical modeling approach to linkage disequilibrium estimation.
P2860
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P2860
Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Shared genomic segment analysi ...... ees using SNP genotype assays.
@ast
Shared genomic segment analysi ...... ees using SNP genotype assays.
@en
Shared genomic segment analysi ...... ees using SNP genotype assays.
@nl
type
label
Shared genomic segment analysi ...... ees using SNP genotype assays.
@ast
Shared genomic segment analysi ...... ees using SNP genotype assays.
@en
Shared genomic segment analysi ...... ees using SNP genotype assays.
@nl
prefLabel
Shared genomic segment analysi ...... ees using SNP genotype assays.
@ast
Shared genomic segment analysi ...... ees using SNP genotype assays.
@en
Shared genomic segment analysi ...... ees using SNP genotype assays.
@nl
P2093
P2860
P1476
Shared genomic segment analysi ...... rees using SNP genotype assays
@en
P2093
K Allen-Brady
L A Cannon-Albright
P2860
P304
P356
10.1111/J.1469-1809.2007.00406.X
P407
P577
2007-12-18T00:00:00Z