130 related articles for article (PubMed ID: 15977179)
1. dbQSNP: a database of SNPs in human promoter regions with allele frequency information determined by single-strand conformation polymorphism-based methods.
Tahira T; Baba S; Higasa K; Kukita Y; Suzuki Y; Sugano S; Hayashi K
Hum Mutat; 2005 Aug; 26(2):69-77. PubMed ID: 15977179
[TBL] [Abstract][Full Text] [Related]
2. Estimation of SNP allele frequencies by SSCP analysis of pooled DNA.
Tahira T; Kukita Y; Higasa K; Okazaki Y; Yoshinaga A; Hayashi K
Methods Mol Biol; 2009; 578():193-207. PubMed ID: 19768595
[TBL] [Abstract][Full Text] [Related]
3. QSNPlite, a software system for quantitative analysis of SNPs based on capillary array SSCP analysis.
Tahira T; Okazaki Y; Miura K; Yoshinaga A; Masumoto K; Higasa K; Kukita Y; Hayashi K
Electrophoresis; 2006 Oct; 27(19):3869-78. PubMed ID: 16960832
[TBL] [Abstract][Full Text] [Related]
4. Identification of disease causing loci using an array-based genotyping approach on pooled DNA.
Craig DW; Huentelman MJ; Hu-Lince D; Zismann VL; Kruer MC; Lee AM; Puffenberger EG; Pearson JM; Stephan DA
BMC Genomics; 2005 Sep; 6():138. PubMed ID: 16197552
[TBL] [Abstract][Full Text] [Related]
5. Direct determination of single nucleotide polymorphism haplotype of NFKBIL1 promoter polymorphism by DNA conformation analysis and its application to association study of chronic inflammatory diseases.
Shibata H; Yasunami M; Obuchi N; Takahashi M; Kobayashi Y; Numano F; Kimura A
Hum Immunol; 2006; 67(4-5):363-73. PubMed ID: 16720219
[TBL] [Abstract][Full Text] [Related]
6. SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries.
Van Tassell CP; Smith TP; Matukumalli LK; Taylor JF; Schnabel RD; Lawley CT; Haudenschild CD; Moore SS; Warren WC; Sonstegard TS
Nat Methods; 2008 Mar; 5(3):247-52. PubMed ID: 18297082
[TBL] [Abstract][Full Text] [Related]
7. Characterization of single-nucleotide polymorphisms in coding regions of human genes.
Cargill M; Altshuler D; Ireland J; Sklar P; Ardlie K; Patil N; Shaw N; Lane CR; Lim EP; Kalyanaraman N; Nemesh J; Ziaugra L; Friedland L; Rolfe A; Warrington J; Lipshutz R; Daley GQ; Lander ES
Nat Genet; 1999 Jul; 22(3):231-8. PubMed ID: 10391209
[TBL] [Abstract][Full Text] [Related]
8. Single nucleotide polymorphism (SNP) allele frequency estimation in DNA pools using Pyrosequencing.
Lavebratt C; Sengul S
Nat Protoc; 2006; 1(6):2573-82. PubMed ID: 17406511
[TBL] [Abstract][Full Text] [Related]
9. High-throughput single nucleotide polymorphism typing by fluorescent single-strand conformation polymorphism analysis with capillary electrophoresis.
Doi K; Doi H; Noiri E; Nakao A; Fujita T; Tokunaga K
Electrophoresis; 2004 Mar; 25(6):833-8. PubMed ID: 15004843
[TBL] [Abstract][Full Text] [Related]
10. SNP-VISTA: an interactive SNP visualization tool.
Shah N; Teplitsky MV; Minovitsky S; Pennacchio LA; Hugenholtz P; Hamann B; Dubchak IL
BMC Bioinformatics; 2005 Dec; 6():292. PubMed ID: 16336665
[TBL] [Abstract][Full Text] [Related]
11. Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection.
Fredman D; Sawyer SL; Strömqvist L; Mottagui-Tabar S; Kidd KK; Wahlestedt C; Chanock SJ; Brookes AJ
Hum Mutat; 2006 Feb; 27(2):173-86. PubMed ID: 16429399
[TBL] [Abstract][Full Text] [Related]
12. Single nucleotide polymorphism in transcriptional regulatory regions and expression of environmentally responsive genes.
Wang X; Tomso DJ; Liu X; Bell DA
Toxicol Appl Pharmacol; 2005 Sep; 207(2 Suppl):84-90. PubMed ID: 16002116
[TBL] [Abstract][Full Text] [Related]
13. A single-strand conformation polymorphism method for the large-scale analysis of mutations/polymorphisms using capillary array electrophoresis.
Kukita Y; Higasa K; Baba S; Nakamura M; Manago S; Suzuki A; Tahira T; Hayashi K
Electrophoresis; 2002 Jul; 23(14):2259-66. PubMed ID: 12210231
[TBL] [Abstract][Full Text] [Related]
14. Allelotyping of pooled DNA with 250 K SNP microarrays.
Wilkening S; Chen B; Wirtenberger M; Burwinkel B; Försti A; Hemminki K; Canzian F
BMC Genomics; 2007 Mar; 8():77. PubMed ID: 17367522
[TBL] [Abstract][Full Text] [Related]
15. The distribution of SNPs in human gene regulatory regions.
Guo Y; Jamison DC
BMC Genomics; 2005 Oct; 6():140. PubMed ID: 16209714
[TBL] [Abstract][Full Text] [Related]
16. Direct determination of MUC5B promoter haplotypes based on the method of single-strand conformation polymorphism and their statistical estimation.
Kamio K; Matsushita I; Tanaka G; Ohashi J; Hijikata M; Nakata K; Tokunaga K; Azuma A; Kudoh S; Keicho N
Genomics; 2004 Sep; 84(3):613-22. PubMed ID: 15498469
[TBL] [Abstract][Full Text] [Related]
17. In silico discrimination of single nucleotide polymorphisms and pathological mutations in human gene promoter regions by means of local DNA sequence context and regularity.
Khan IA; Mort M; Buckland PR; O'Donovan MC; Cooper DN; Chuzhanova NA
In Silico Biol; 2006; 6(1-2):23-34. PubMed ID: 16789908
[TBL] [Abstract][Full Text] [Related]
18. Usefulness of direct sequencing of pooled DNA for SNP identification and allele-frequency determination compatible with a common disease/common variant hypothesis.
Kim MK; Nam TS; Choi KH; Jang SY; Kim YO; Lee MC
Genet Mol Res; 2010 Apr; 9(2):772-9. PubMed ID: 20449810
[TBL] [Abstract][Full Text] [Related]
19. Frequency Finder: a multi-source web application for collection of public allele frequencies of SNP markers.
Nguyen TH; Liu C; Gershon ES; McMahon FJ
Bioinformatics; 2004 Feb; 20(3):439-43. PubMed ID: 14960477
[TBL] [Abstract][Full Text] [Related]
20. Pyrosequencing-based SNP allele frequency estimation in DNA pools.
Lavebratt C; Sengul S; Jansson M; Schalling M
Hum Mutat; 2004 Jan; 23(1):92-7. PubMed ID: 14695537
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
