(2008) VarDetect: a nucleotide sequence variation exploratory tool, BMC Bioinformatics 9 Suppl 12, S9. Ngamphiw, C., Kulawonganunchai, S., Assawamakin, A., Jenwitheesuk, E., Tongsima, S.(2007) PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data, Genome Res 17, 659–666. (2007) AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes, Bioinformatics 23, 1689–1691. W., Stephens, P., Raine, K., Yates, A., Mattocks, C., Tarpey, P., Butler, A., Menzies, A., Richardson, D., Jenkinson, A., Davies, H., Edkins, S., Forbes, S., Gray, K., Greenman, C., Shepherd, R., Stratton, M. Error probabilities, Genome Res 8, 186–194. (1998) Base-calling of automated sequencer traces using Phred. (2005) SeqDoC: rapid SNP and mutation detection by direct comparison of DNA sequence chromatograms, BMC Bioinformatics 6, 133. (2005) InSNP: a tool for automated detection and visualization of SNPs and InDels, Hum Mutat 26, 11–19. Manaster, C., Zheng, W., Teuber, M., Wachter, S., Doring, F., Schreiber, S., Hampe, J.(2005) novoSNP, a novel computational tool for sequence variation discovery, Genome Res 15, 436–442. Weckx, S., Del-Favero, J., Rademakers, R., Claes, L., Cruts, M., De Jonghe, P., Van Broeckhoven, C., De Rijk, P.(2005) SNPdetector: a software tool for sensitive and accurate SNP detection, PLoS Comput Biol 1, e53. A., Yakub, I., Wei, S., Sood, R., Rowe, W., Liu, P. (2003) Automated identification of single nucleotide polymorphisms from sequencing data, J Bioinform Comput Biol 1, 253–265. Takahashi, M., Matsuda, F., Margetic, N., Lathrop, M.(1999) A general approach to single-nucleotide polymorphism discovery, Nat Genet 23, 452–456. (2001) Automated fluorescent DNA sequencing on the ABI PRISM 377, Methods Mol Biol 167, 119–152. (1992) DNA sequencing with chain-terminating inhibitors.
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