Modeling and optimization of genetic screens via RNA interference and FACS
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Abstract: We study mathematically a method for discovering which gene is related to a cell phenotype of interest. The method is based on RNA interference -- a molecular process for gene deactivation -- and on coupling the phenotype with fluorescence in a FACS machine. A small number of candidate genes are thus isolated, and then tested individually. We model probabilistically this process, prove a limit theorem for its outcome, and derive operational guidelines for maximizing the probability of successful gene discovery.
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- A hybrid algorithm for the DNA sequencing problem
- A hyper-heuristic approach to sequencing by hybridization of DNA sequences
- DNA Sequencing by Hybridization via Genetic Search
- Immortal branching Markov processes: Averaging properties and PCR applications.
- On estimation of a class of efficacy-related parameters
- Optimal Protein Structure Alignment Using Maximum Cliques
- Some operations research methods for analyzing protein sequences and structures
- Weak convergence and empirical processes. With applications to statistics
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