Incorporating linkage information into a common disease/rare variant framework.
about
PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markersLinkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide associationLessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysisFamily-based approaches: design, imputation, analysis, and beyond.Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysisIdentification of rare variants from exome sequence in a large pedigree with autism.Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes.Population-based and family-based designs to analyze rare variants in complex diseases.
P2860
Q30984320-B8E0F037-A5AE-42C0-9781-68411C63BE01Q34319603-A0D1726A-3954-4B7E-B5EC-A248F6477504Q35751969-75B60A37-72B0-4626-A777-863CFB656C4DQ35920732-0067BA15-646D-4156-8BE0-936E7A40F7B3Q36686743-CB9720F1-88C4-438D-80B3-A0943A14F402Q37042364-48285116-029B-4C6D-BD0B-4CB0A7919922Q37646569-0FBEFF36-6E07-4F6F-85F0-7BE5A5487FCCQ41886407-DAFE8A52-D47E-448C-8112-948E6C3ECC53
P2860
Incorporating linkage information into a common disease/rare variant framework.
description
2011 nî lūn-bûn
@nan
2011年の論文
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2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Incorporating linkage information into a common disease/rare variant framework.
@ast
Incorporating linkage information into a common disease/rare variant framework.
@en
type
label
Incorporating linkage information into a common disease/rare variant framework.
@ast
Incorporating linkage information into a common disease/rare variant framework.
@en
prefLabel
Incorporating linkage information into a common disease/rare variant framework.
@ast
Incorporating linkage information into a common disease/rare variant framework.
@en
P2860
P356
P1433
P1476
Incorporating linkage information into a common disease/rare variant framework.
@en
P2093
Anthony L Hinrichs
Brian K Suarez
P2860
P356
10.1002/GEPI.20654
P478
35 Suppl 1
P577
2011-01-01T00:00:00Z