A more complete haplotype prediction is still a mathematical calculation, and storing and providing it adds nothing
In re Board of Trustees of the Leland Stanford Junior University, 989 F.3d 1367, No. 2020-1012 (Fed. Cir. Mar. 11, 2021) (precedential) (Reyna, J., joined by Prost, C.J., and Lourie, J.), affirming the Patent Trial and Appeal Board's rejection of claims 1, 4 through 11, 14 through 25 and 27 through 30 of United States Patent Application No. 13/445,925
United States Patent Application No. 13/445,925, filed by Stanford on April 13, 2012, claims a method for resolving haplotype phase, the determination of which parent an allele was inherited from. Claim 1 recites receiving allele data for a family of two parents and at least two children, receiving pedigree data, determining an inheritance state using a hidden Markov model with specified hidden states, receiving transition probability data and population linkage disequilibrium data, determining a haplotype phase from those inputs, storing it, and providing it in response to a request, each step on a computer system comprising a processor and a memory. The specification reports phase resolution of 97.9 percent of heterozygous positions against roughly 80 percent for the prior method. The examiner rejected the claims under Section 101 of Title 35 of the United States Code, the Board affirmed, and the Federal Circuit affirmed. At step one claim 1 is directed to the abstract idea of mathematically calculating alleles' haplotype phase, recites no concrete application for the haplotype phase beyond storing it and providing it upon request, and a greater number of predictions is not an improved technological process. At step two the hardware was generic, the mathematical steps and data types conventional according to the specification itself, and the ordered combination unexplained. Dependent claims adding diagnosis, drug treatment and prognosis determinations instruct only to apply the algorithm.
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