92 related articles for article (PubMed ID: 19957144)
1. SNP-PHAGE: high-throughput SNP discovery pipeline.
Aransay AM; Matthiesen R; Regueiro MM
Methods Mol Biol; 2010; 593():49-65. PubMed ID: 19957144
[TBL] [Abstract][Full Text] [Related]
2. High-throughput methods for SNP genotyping.
Ding C; Jin S
Methods Mol Biol; 2009; 578():245-54. PubMed ID: 19768599
[TBL] [Abstract][Full Text] [Related]
3. SNP-PHAGE--High throughput SNP discovery pipeline.
Matukumalli LK; Grefenstette JJ; Hyten DL; Choi IY; Cregan PB; Van Tassell CP
BMC Bioinformatics; 2006 Oct; 7():468. PubMed ID: 17059604
[TBL] [Abstract][Full Text] [Related]
4. New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies.
De La Vega FM; Dailey D; Ziegle J; Williams J; Madden D; Gilbert DA
Biotechniques; 2002 Jun; Suppl():48-50, 52, 54. PubMed ID: 12083398
[TBL] [Abstract][Full Text] [Related]
5. Tag SNP selection for association studies.
Stram DO
Genet Epidemiol; 2004 Dec; 27(4):365-74. PubMed ID: 15372618
[TBL] [Abstract][Full Text] [Related]
6. Assessment of two flexible and compatible SNP genotyping platforms: TaqMan SNP Genotyping Assays and the SNPlex Genotyping System.
De la Vega FM; Lazaruk KD; Rhodes MD; Wenz MH
Mutat Res; 2005 Jun; 573(1-2):111-35. PubMed ID: 15829242
[TBL] [Abstract][Full Text] [Related]
7. Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels.
Goode EL; Jarvik GP
Genet Epidemiol; 2005; 29 Suppl 1():S72-6. PubMed ID: 16342185
[TBL] [Abstract][Full Text] [Related]
8. Basic molecular techniques for the detection of single nucleotide polymorphisms: genome-wide applications in search for endocrine tumor related genes.
Horvath A; Stratakis C
Methods Mol Biol; 2009; 590():143-63. PubMed ID: 19763502
[TBL] [Abstract][Full Text] [Related]
9. High-throughput single-nucleotide polymorphism analysis of the IL1RN locus in patients with ankylosing spondylitis by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry.
Maksymowych WP; Reeve JP; Reveille JD; Akey JM; Buenviaje H; O'Brien L; Peloso PM; Thomson GT; Jin L; Russell AS
Arthritis Rheum; 2003 Jul; 48(7):2011-8. PubMed ID: 12847695
[TBL] [Abstract][Full Text] [Related]
10. High-throughput identification, database storage and analysis of SNPs in EST sequences.
Useche FJ; Gao G; Harafey M; Rafalski A
Genome Inform; 2001; 12():194-203. PubMed ID: 11791238
[TBL] [Abstract][Full Text] [Related]
11. A haplotype sharing method for determining the relative age of SNP alleles.
de Vries AR; te Meerman GJ
Hum Hered; 2010; 69(1):52-9. PubMed ID: 19797909
[TBL] [Abstract][Full Text] [Related]
12. Two-Stage sampling designs for gene association studies.
Thomas D; Xie R; Gebregziabher M
Genet Epidemiol; 2004 Dec; 27(4):401-14. PubMed ID: 15543639
[TBL] [Abstract][Full Text] [Related]
13. [Host genetic epidemiology by single nucleotide polymorphism(SNP) analysis].
Shin HD
Exp Mol Med; 2001 Apr; 33(1 Suppl):51-69. PubMed ID: 11708326
[TBL] [Abstract][Full Text] [Related]
14. [Analysis and application of SNP and haplotype in the human genome].
Li J; Pan YC; Li YX; Shi TL
Yi Chuan Xue Bao; 2005 Aug; 32(8):879-89. PubMed ID: 16231744
[TBL] [Abstract][Full Text] [Related]
15. Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes.
Morris AP
Genet Epidemiol; 2005 Sep; 29(2):91-107. PubMed ID: 15940704
[TBL] [Abstract][Full Text] [Related]
16. Quantifying the amount of missing information in genetic association studies.
Nicolae DL
Genet Epidemiol; 2006 Dec; 30(8):703-17. PubMed ID: 16986163
[TBL] [Abstract][Full Text] [Related]
17. SNP genotyping by the 5'-nuclease reaction: advances in high-throughput genotyping with nonmodel organisms.
Seeb JE; Pascal CE; Ramakrishnan R; Seeb LW
Methods Mol Biol; 2009; 578():277-92. PubMed ID: 19768601
[TBL] [Abstract][Full Text] [Related]
18. Single nucleotide polymorphism genotyping: biochemistry, protocol, cost and throughput.
Chen X; Sullivan PF
Pharmacogenomics J; 2003; 3(2):77-96. PubMed ID: 12746733
[TBL] [Abstract][Full Text] [Related]
19. The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers.
Ohashi J; Tokunaga K
J Hum Genet; 2001; 46(8):478-82. PubMed ID: 11501946
[TBL] [Abstract][Full Text] [Related]
20. A whole genome scan to map QTL for milk production traits and somatic cell score in Canadian Holstein bulls.
Kolbehdari D; Wang Z; Grant JR; Murdoch B; Prasad A; Xiu Z; Marques E; Stothard P; Moore SS
J Anim Breed Genet; 2009 Jun; 126(3):216-27. PubMed ID: 19646150
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
