Genome mapping by nonrandom anchoring: a discrete theoretical analysis.
Genome mapping by nonrandom anchoring: a discrete theoretical analysis.
复制标题
通过非随机锚定进行基因组作图:离散理论分析。
DOI:
10.1073/pnas.90.2.600
复制
发表时间:
1993
影响因子:
11.1
通讯作者:
Marr,TG
中科院分区:
文献类型:
--
作者:
Zhang,MQ;Marr,TG
As part of our effort to construct a physical map of the genome of the fission yeast Schizosaccharomyces pombe, we have made theoretical predictions for the progress expected, as measured by the expected length fraction of island coverage and by the expected properties of the anchored islands such as the number and the size of islands. Our experimental strategy is to construct a random clone library and screen the library for clones having unique sequence at both ends. This scheme is essentially the same as the clone-limited double sequence-tagged-site selection scheme which was used in a computer simulation by Palazzolo et al. [Palazzolo, M. J., Sawyer, S. A., Martin, C. H., Smoller, D. A. & Hartl, D. L. (1991) Proc. Natl. Acad. Sci. USA 88, 8034-8038]. Both simulation and ongoing experiments in our laboratory have shown that the nonrandom anchoring method is far superior to random anchoring. In this paper, we propose a theoretical model to explain the simulated data and the experimental data.