Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array
about
Specific and complete human genome amplification with improved yield achieved by phi29 DNA polymerase and a novel primer at elevated temperatureHuman genetics and genomics a decade after the release of the draft sequence of the human genomeEvaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individualsChallenges in the association of human single nucleotide polymorphism mentions with unique database identifiersInferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arraysMultiplex amplification enabled by selective circularization of large sets of genomic DNA fragmentsHighly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assayMapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of functionAssociation of single nucleotide polymorphisms in PIM-1 gene with the risk of Korean lung cancerA comprehensive assay for targeted multiplex amplification of human DNA sequencesThe application of single nucleotide polymorphism microarrays in cancer researchComparative linkage analysis and visualization of high-density oligonucleotide SNP array dataPPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays.Identification of disease causing loci using an array-based genotyping approach on pooled DNA.SNiPer: improved SNP genotype calling for Affymetrix 10K GeneChip microarray dataEvaluation of multiple displacement amplification in a 5 cM STR genome-wide scan.Effects of DNA mass on multiple displacement whole genome amplification and genotyping performance.CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Genomic-Wide Analysis with Microarrays in Human OncologyWhole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellitesWhole-genome association study of bipolar disorderCranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 geneLoss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosisGenomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arraysMutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disabilityA HapMap harvest of insights into the genetics of common diseaseGenome-wide association studies for common diseases and complex traitsPrecision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae statisticsAccuTyping: new algorithms for automated analysis of data from high-throughput genotyping with oligonucleotide microarrays.Contribution of Asian mouse subspecies Mus musculus molossinus to genomic constitution of strain C57BL/6J, as defined by BAC-end sequence-SNP analysisGenomic profiling by DNA amplification of laser capture microdissected tissues and array CGHComparing single-nucleotide polymorphism marker-based and microsatellite marker-based linkage analyses.Bias of allele-sharing linkage statistics in the presence of intermarker linkage disequilibriumEvaluation of linkage disequilibrium and its effect on non-parametric multipoint linkage analysis using two high density single-nucleotide polymorphism mapping panels.TAMGeS: a Three-array Method for Genotyping of SNPs by a dual-colour approach.A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer.High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays.Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes
P2860
Q21202149-3FCC87AA-F1CD-4021-8D69-A740F9856BF8Q21245451-4F5B115F-1BEB-4C09-BF84-DB4FA0A21755Q21263176-10F44281-D4EE-4679-97C1-E960ADDB713DQ21284327-7F93004D-FB35-45AD-BE51-BADC6D2D8FC3Q21563517-A14CF068-5531-43EC-AE29-C0EFAD872695Q24523669-4FA8EF2D-62FB-4750-8C70-7E582AE0D0F5Q24557419-BDDB1369-207F-43A0-9C3A-A57458FE9996Q24564082-099A5FD7-7E2C-478D-902B-25203E7329F9Q24645195-2FCD96CC-F6B5-4E04-8772-61F342B15B64Q24647956-76E6CA19-612D-4DF6-B02C-B4F601F84C49Q24653582-A8E00387-8ECE-4087-8CD8-FF9E5A7853D2Q24797003-95343C6B-9575-47F3-AFE6-985DC675D08EQ24810725-32102741-6220-48E1-8D4F-25CEB139F4F4Q24815025-CE454D35-F8A9-4AB2-B824-F9FE227410E5Q24815814-8194BABA-6796-4B8A-AAEE-02F9A9A7D2DCQ24816052-D4F51E35-70AC-4476-8B61-9DDA7539F60BQ24816650-FD5E9F65-04B3-4E18-B1C8-C12A8CACFCC5Q25257143-CD1DFEC1-2FA8-4E0C-B089-8B3F672F05E8Q28081059-50E4100C-B7C2-4B9A-8B7F-473BD3949FBFQ28262660-F2D9448E-27C0-4C65-9E59-6C1086B5238DQ28271419-C13873E4-946F-46A1-8A32-4704D6343655Q28283137-1DC8C685-2D9C-460A-927B-7E0E46B4EA76Q28288338-3B450817-BA28-40B7-AB52-D84575FF564DQ28294932-DDAAC38D-53AB-45A5-B208-B150A783D0D9Q28302878-85A6D6E6-F66F-4227-A870-F23FC4DD2B51Q28757788-89A961B9-C3DA-4A1B-A784-0B68D1A0D937Q29147451-5345083C-A13C-4BA3-93DC-24F016AAAD89Q29614875-678603CE-CC6A-4E13-9F50-568B7A81309DQ29615822-516A220A-7F3C-46E3-BC8F-02127AD93F14Q31031507-82993F74-4BA1-4410-9820-96432A642814Q31061489-9BD7A7DB-BF03-4229-8B38-4971C917EC85Q31133403-1B88A3D4-9D98-4548-B1E1-CD35B5110521Q33208489-E12A1D93-B904-4482-8FD4-8421DDE92075Q33232722-9C20A0D9-A9E2-4C44-B381-699DF9D3F292Q33232837-3C695939-3BF9-4F9D-9CDA-77040F35014EQ33232839-E81C1782-895B-451C-8FF2-C4709BC40860Q33268700-09626581-ED34-452D-8478-C8E39F035C52Q33269177-186ABA11-8953-4AA3-970E-BBC6058E8B93Q33271277-9AE3D96D-DEF0-4D93-9C57-98D3A5D8C136Q33326165-6723D581-0F9D-4F78-A4D1-841077FE5757
P2860
Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Parallel genotyping of over 10 ...... -density oligonucleotide array
@ast
Parallel genotyping of over 10 ...... -density oligonucleotide array
@en
type
label
Parallel genotyping of over 10 ...... -density oligonucleotide array
@ast
Parallel genotyping of over 10 ...... -density oligonucleotide array
@en
prefLabel
Parallel genotyping of over 10 ...... -density oligonucleotide array
@ast
Parallel genotyping of over 10 ...... -density oligonucleotide array
@en
P2093
P2860
P356
P1433
P1476
Parallel genotyping of over 10 ...... -density oligonucleotide array
@en
P2093
Geoffrey Yang
Giulia C Kennedy
Gregory A Marcus
Guoying Liu
Hajime Matsuzaki
Halina Loi
Jennifer M Puck
Jing Huang
P2860
P304
P356
10.1101/GR.2014904
P577
2004-03-01T00:00:00Z