Whole-genome genotyping with the single-base extension assay.
about
Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variantsMicroRNA-related genetic variations as predictors for risk of second primary tumor and/or recurrence in patients with early-stage head and neck cancerCopy number variation at 1q21.1 associated with neuroblastomaAn integrated genomic analysis of human glioblastoma multiformeIntegrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancersSequencing by Cyclic Ligation and Cleavage (CycLiC) directly on a microarray captured template.The application of single nucleotide polymorphism microarrays in cancer researchChromosome 6p22 locus associated with clinically aggressive neuroblastomaAssociation of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's diseaseGenomic Regions Associated With Interspecies Communication in Dogs Contain Genes Related to Human Social Disorders.Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's diseaseSingleton SNPs in the human genome and implications for genome-wide association studiesDevelopment of a large SNP genotyping array and generation of high-density genetic maps in tomatoA large maize (Zea mays L.) SNP genotyping array: development and germplasm genotyping, and genetic mapping to compare with the B73 reference genomeResolving the evolution of extant and extinct ruminants with high-throughput phylogenomicsCommon variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastomaMassive screening of copy number population-scale variation in Bos taurus genomeFollow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.A HapMap harvest of insights into the genetics of common diseaseLoci influencing lipid levels and coronary heart disease risk in 16 European population cohortsImproving the accuracy and efficiency of identity-by-descent detection in population dataMeta-analysis of human methylation data for evidence of sex-specific autosomal patterns.Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray.QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.A new model calling procedure for Illumina BeadArray data.High quality genome-wide genotyping from archived dried blood spots without DNA amplification.Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project.Sequencing-based variant detection in the polyploid crop oilseed rape.Comparison of PrASE and Pyrosequencing for SNP Genotyping.TAMGeS: a Three-array Method for Genotyping of SNPs by a dual-colour approach.Efficient target-selected mutagenesis in Caenorhabditis elegans: toward a knockout for every gene.Power to detect risk alleles using genome-wide tag SNP panelsEnhancing genetic mapping of complex genomes through the design of highly-multiplexed SNP arrays: application to the large and unsequenced genomes of white spruce and black spruceGoldsurfer2 (Gs2): a comprehensive tool for the analysis and visualization of genome wide association studies.Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies.A flexible rank-based framework for detecting copy number aberrations from array data.Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.Assessment of DNA extracted from FTA cards for use on the Illumina iSelect BeadChip.
P2860
Q24624194-C2A9377E-293F-4B44-BE43-44A969479F15Q24629078-B056858B-1C33-4F14-9826-E8E3A32B5333Q24642330-5983B216-A78F-4EDC-A620-EB749C04FBC8Q24648860-57C526EA-DB8C-4099-BADD-22A9DF0EF613Q24649562-47D72588-22B8-4B6D-BE77-B032EABD4330Q24652505-43C45B2E-C0B1-446F-A4FE-DA7FE28877B6Q24653582-35597937-820B-4239-BA74-F5E0F818C01EQ24656264-9D085D15-13B9-462C-BA51-750D055795BCQ24673589-A1036047-084D-495B-83EE-03665165D73DQ27347958-FD7092BF-0BCD-4C64-BAB6-7C38167469C7Q28235756-E29FC138-33B2-479A-BDC9-BA005F3F1951Q28264742-9FA15FE1-6AC1-427D-B287-A40282B04C62Q28727319-6519FE7E-A1BB-4EB6-B44C-08F74047B18FQ28741696-EA894388-4B41-4415-9D69-167FF4800344Q28750433-D30F0F62-6D29-41A5-A58E-CCCC90DE2CACQ28943271-BC46F1E7-5380-4A2B-B69F-CF05B814FF14Q29048172-9378DF25-221B-491B-915E-476B7700CBF7Q29417127-A9F59725-E534-4B42-9E50-62458AE77891Q29614875-25D3A3B4-734C-4703-9BFE-1F8A5275A8F6Q29614946-0D179E5D-6A2B-4526-B719-43E199F5A293Q30608038-B4630C2E-A80B-4929-A769-170EDD08DA5FQ30870463-29824864-8CE5-46C7-94BF-8E540C3F4570Q31002427-A6AA4C84-12EC-49E9-B4EA-C18D861B3B39Q31104515-493F6D1D-96BA-4D3D-82EA-F4192F204736Q31110585-D2BD1B00-F150-4151-AAF1-29E345A6DC62Q31118824-79D8AD17-B218-4FC8-99BF-078F2BF76067Q31120402-60D002B1-D7F3-4723-9FAC-D6DC8041D239Q31125811-18AD0297-E9E7-4083-A14D-BB4B0B7294D7Q33263696-48C72451-AD51-469C-90D8-E5999A85DB5CQ33268700-EB6C83AF-755A-4B2C-ABA4-9D8E82CE44CDQ33281454-5B0DDF15-8817-42AC-9627-EABF7A7BCB54Q33301926-B0FEF5F3-5871-477F-9F84-61250DDE86E6Q33315464-C5A9D0F6-EB9C-465C-A0C0-F5B71284129FQ33322404-1E4A87D7-732E-4C59-94B7-0E4A6735022DQ33323357-2014CDE6-BF63-4C84-9B8F-8EF0A60C8DACQ33373518-53C80B92-05EF-4ED1-AF4E-10AC2C20329FQ33381588-7991A168-357D-4026-980B-88DC52E8FB09Q33403709-4F32C8E2-E7F2-4775-B4F3-4F56A9BE2F10Q33455772-B3A35A57-57D6-4983-AD19-FC1AE76EDA18Q33468651-DED1DA16-09F7-4D8F-A859-63A7E27F6A65
P2860
Whole-genome genotyping with the single-base extension assay.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Whole-genome genotyping with the single-base extension assay.
@en
Whole-genome genotyping with the single-base extension assay.
@nl
type
label
Whole-genome genotyping with the single-base extension assay.
@en
Whole-genome genotyping with the single-base extension assay.
@nl
prefLabel
Whole-genome genotyping with the single-base extension assay.
@en
Whole-genome genotyping with the single-base extension assay.
@nl
P2093
P356
P1433
P1476
Whole-genome genotyping with the single-base extension assay.
@en
P2093
David L Barker
Frank J Steemers
Kevin L Gunderson
Richard Shen
Weihua Chang
P2888
P356
10.1038/NMETH842
P577
2006-01-01T00:00:00Z