Prediction of disease-causing alleles from sequence context

作者: Alexander Pertsemlidis , Monica Horvath , Harold Garner , John Fondon

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摘要: An apparatus, system and method for predicting single nucleotide polymorphisms (SNPs) is disclosed. The present invention generally includes steps obtaining a variation predictiveness matrix one or more variations of nucleic acid sequence based on the matrix. may be made by calculating frequency from first base to second in dataset two bases determining value calculated frequency.

参考文章(2)
John D. Minna, Jonathan D. Wren, Harold R. Garner, John W. Fondon, Polymorphic repeats in human genes ,(1999)
Laura L. Stuve, Tod M. Klingler, Philippe E. Rigault, David A. Hadley, Anne L. Curtis, Robert E. Lagace, Michael P. Wood, Michael G. Walker, Harold H. Hibbert, Richard D. Goold, System and method for a precompiled database for biomolecular sequence information ,(2001)