Comparison of GenFlex Tag array and Pyrosequencing in SNP genotyping.
暂无分享,去创建一个
[1] L. Peltonen,et al. Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24. , 2002, Human molecular genetics.
[2] P. Visscher,et al. SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis. , 2002, Nucleic acids research.
[3] Ching Yu Austin Huang,et al. SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery. , 2002, BioTechniques.
[4] A. Syvänen. Accessing genetic variation: genotyping single nucleotide polymorphisms , 2001, Nature Reviews Genetics.
[5] A Chakravarti,et al. High-throughput variation detection and genotyping using microarrays. , 2001, Genome research.
[6] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .
[7] K. Lindblad-Toh,et al. SBE-TAGS: an array-based method for efficient single-nucleotide polymorphism genotyping. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[8] P. S. White,et al. Flow cytometry-based minisequencing: a new platform for high-throughput single-nucleotide polymorphism scoring. , 2000, Genomics.
[9] A Chakravarti,et al. Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays. , 2000, Genome research.
[10] B. Beghé,et al. Comparison of three methods for single nucleotide polymorphism typing for DNA bank studies: Sequence‐specific oligonucleotide probe hybridisation, TaqMan liquid phase hybridisation, and microplate array diagonal gel electrophoresis (MADGE) , 1999, Human mutation.
[11] D Ryan,et al. Non-PCR-dependent detection of the factor V Leiden mutation from genomic DNA using a homogeneous invader microtiter plate assay. , 1999, Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology.
[12] P. Kwok,et al. Fluorescence polarization in homogeneous nucleic acid analysis. , 1999, Genome research.
[13] M. Ronaghi,et al. A Sequencing Method Based on Real-Time Pyrophosphate , 1998, Science.
[14] K. Livak,et al. A homogeneous, ligase-mediated DNA diagnostic test. , 1998, Genome research.
[15] M. Daly,et al. Genomewide scan of multiple sclerosis in Finnish multiplex families. , 1997, American journal of human genetics.
[16] A. Palotie,et al. Towards automatic detection of point mutations: use of scintillating microplates in solid-phase minisequencing. , 1994, BioTechniques.
[17] K Kontula,et al. A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E. , 1990, Genomics.
[18] Mats Nilsson,et al. Oligonucleotide ligation assay. , 2003, Methods in molecular biology.
[19] E. Eichler,et al. Segmental duplications and the evolution of the primate genome , 2002, Nature Reviews Genetics.
[20] C. Cantor,et al. Automated genotyping using the DNA MassArray technology. , 2001, Methods in molecular biology.
[21] E. Lander,et al. Characterization of single-nucleotide polymorphisms in coding regions of human genes , 1999, Nature Genetics.