CPC G16B 30/10 (2019.02) [G06N 3/126 (2013.01); G16B 20/00 (2019.02); G16B 20/20 (2019.02); G16B 30/00 (2019.02); G16H 50/00 (2018.01); C12Q 1/68 (2013.01)] | 20 Claims |
1. A method for genetic analysis of a subject, comprising:
(a) subjecting a first nucleic acid sample of said subject to an untargeted sequencing reaction to generate a first set of sequencing data, wherein said first set of sequencing data comprises 300 megabases;
(b) subjecting a second nucleic acid sample of said subject to a target-specific sequencing reaction to generate a second set of sequencing data comprising RNA sequencing data; and
(c) using a computer to generate a combined output from said first set of sequencing data and said second set of sequencing data, which combined output is indicative of a presence or absence of one or more polymorphisms in at least a portion of a genome of said subject.
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