Making 'random amplification' predictable in whole genome analysis.
暂无分享,去创建一个
[1] Timothy B. Stockwell,et al. The Sequence of the Human Genome , 2001, Science.
[2] N. Carter,et al. Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. , 1992, Genomics.
[3] C. Nusbaum,et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. , 1998, Science.
[4] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[5] L. Kruglyak. Prospects for whole-genome linkage disequilibrium mapping of common disease genes , 1999, Nature Genetics.
[6] P. Kwok,et al. Methods for genotyping single nucleotide polymorphisms. , 2003, Annual review of genomics and human genetics.
[7] David E. Housman,et al. Genome complexity reduction for SNP genotyping analysis , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[8] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[9] H. Himmelbauer,et al. Interspersed repetitive sequence (IRS)-PCR for typing of whole genome radiation hybrid panels. , 2000, Nucleic acids research.