These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
66 related articles for article (PubMed ID: 22311482)
1. [Application of SNPstream for medical genetics research]. Fei LJ; Ji LD; Zhang LN; Hua S; Jin JQ; Xu J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):9-12. PubMed ID: 22311482 [TBL] [Abstract][Full Text] [Related]
2. SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery. Bell PA; Chaturvedi S; Gelfand CA; Huang CY; Kochersperger M; Kopla R; Modica F; Pohl M; Varde S; Zhao R; Zhao X; Boyce-Jacino MT; Yassen A Biotechniques; 2002 Jun; Suppl():70-2, 74, 76-7. PubMed ID: 12083401 [TBL] [Abstract][Full Text] [Related]
3. High-throughput genotyping system as a robust and useful tool in oncology: experience from a single institution. Henríquez-Hernández LA; Valenciano A; Herrera-Ramos E; Lloret M; Riveros-Perez A; Lara PC Biologicals; 2013 Nov; 41(6):424-9. PubMed ID: 24103542 [TBL] [Abstract][Full Text] [Related]
4. Comparison of PrASE and Pyrosequencing for SNP Genotyping. Käller M; Hultin E; Holmberg K; Persson ML; Odeberg J; Lundeberg J; Ahmadian A BMC Genomics; 2006 Nov; 7():291. PubMed ID: 17107626 [TBL] [Abstract][Full Text] [Related]
5. Typing of 49 autosomal SNPs by single base extension and capillary electrophoresis for forensic genetic testing. Børsting C; Tomas C; Morling N Methods Mol Biol; 2012; 830():87-107. PubMed ID: 22139655 [TBL] [Abstract][Full Text] [Related]
6. Genotyping of human platelet antigen-15 by single closed-tube Tm-shift method. Zhou SH; Liu M; An WX; Liang XH; Yu WJ; Gong BL; Piao FY Int J Lab Hematol; 2012 Feb; 34(1):41-6. PubMed ID: 21668657 [TBL] [Abstract][Full Text] [Related]
7. The GoldenGate genotyping assay: custom design, processing, and data analysis. González-Neira A Methods Mol Biol; 2013; 1015():147-53. PubMed ID: 23824854 [TBL] [Abstract][Full Text] [Related]
8. A comparison between SNaPshot, pyrosequencing, and biplex invader SNP genotyping methods: accuracy, cost, and throughput. Pati N; Schowinsky V; Kokanovic O; Magnuson V; Ghosh S J Biochem Biophys Methods; 2004 Jul; 60(1):1-12. PubMed ID: 15236905 [TBL] [Abstract][Full Text] [Related]
9. Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers. Goddard KA; Wijsman EM Genet Epidemiol; 2002 Mar; 22(3):205-20. PubMed ID: 11921081 [TBL] [Abstract][Full Text] [Related]
10. [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]
11. Enhanced discrimination of single nucleotide polymorphism in genotyping by phosphorothioate proofreading allele-specific amplification. Hu YJ; Li ZF; Diamond AM Anal Biochem; 2007 Oct; 369(1):54-9. PubMed ID: 17631854 [TBL] [Abstract][Full Text] [Related]
12. Towards low cost, multiplex clinical genotyping: 4-fluorescent Kompetitive Allele-Specific PCR and its application on pharmacogenetics. Suo W; Shi X; Xu S; Li X; Lin Y PLoS One; 2020; 15(3):e0230445. PubMed ID: 32176732 [TBL] [Abstract][Full Text] [Related]
13. Quantitative genotyping of single nucleotide polymorphism by single-molecule multi-color fluorescence resonance energy transfer. Koh HR; Han KY; Jung J; Kim SK Chem Commun (Camb); 2011 Oct; 47(37):10362-4. PubMed ID: 21847490 [TBL] [Abstract][Full Text] [Related]
14. Further development of multiplex single nucleotide polymorphism typing method, the DigiTag2 assay. Nishida N; Tanabe T; Takasu M; Suyama A; Tokunaga K Anal Biochem; 2007 May; 364(1):78-85. PubMed ID: 17359929 [TBL] [Abstract][Full Text] [Related]
15. Hot topic: performance of bovine high-density genotyping platforms in Holsteins and Jerseys. Rincon G; Weber KL; Eenennaam AL; Golden BL; Medrano JF J Dairy Sci; 2011 Dec; 94(12):6116-21. PubMed ID: 22118099 [TBL] [Abstract][Full Text] [Related]
16. Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry. Werner M; Sych M; Herbon N; Illig T; König IR; Wjst M Hum Mutat; 2002 Jul; 20(1):57-64. PubMed ID: 12112658 [TBL] [Abstract][Full Text] [Related]
17. Specificity of genetic diversity in D1S80 revealed by SNP-VNTR haplotyping. Limborska SA; Khrunin AV; Flegontova OV; Tasitz VA; Verbenko DA Ann Hum Biol; 2011 Sep; 38(5):564-9. PubMed ID: 21834750 [TBL] [Abstract][Full Text] [Related]
18. A fast modified protocol for random-access ultra-high density whole-genome scan: a tool for personalized genomic medicine, positional mapping, and cytogenetic analysis. Lau KC; Mak CM; Leung KY; Tsoi TH; Tang HY; Lee P; Lam CW Clin Chim Acta; 2009 Aug; 406(1-2):31-5. PubMed ID: 19445911 [TBL] [Abstract][Full Text] [Related]
19. Automation in genotyping of single nucleotide polymorphisms. Gut IG Hum Mutat; 2001 Jun; 17(6):475-92. PubMed ID: 11385706 [TBL] [Abstract][Full Text] [Related]
20. Pharmacogenetics and genotyping: on the trail of SNPs. Melton L Nature; 2003 Apr; 422(6934):917, 919, 921, 923. PubMed ID: 12712209 [No Abstract] [Full Text] [Related] [Next] [New Search]