Learning from Data-Rich Problems: A Case Study on Genetic Variant Calling

12 Nov 2019Ren YiPi-Chuan ChangGunjan BaidAndrew Carroll

Next Generation Sequencing can sample the whole genome (WGS) or the 1-2% of the genome that codes for proteins called the whole exome (WES). Machine learning approaches to variant calling achieve high accuracy in WGS data, but the reduced number of training examples causes training with WES data alone to achieve lower accuracy... (read more)

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