Abstract

We present an ultrafast method for comparing personal genomes. We transform the standard genome representation (lists of variants relative to a reference) into “genome fingerprints” via locality sensitive hashing. The resulting genome fingerprints can be meaningfully compared even when the input data were obtained using different sequencing technologies, processed using different pipelines, represented in different data formats and relative to different reference versions. Furthermore, genome fingerprints are robust to up to 30% missing data. Because of their reduced size, computation on the genome fingerprints is fast and requires little memory. For example, we could compute all-against-all pairwise comparisons among the 2504 genomes in the 1000 Genomes data set in 67 s at high quality (21 μs per comparison, on a single processor), and achieved a lower quality approximation in just 11 s. Efficient computation enables scaling up a variety of important genome analyses, including quantifying relatedness, recognizing duplicative sequenced genomes in a set, population reconstruction, and many others. The original genome representation cannot be reconstructed from its fingerprint, effectively decoupling genome comparison from genome interpretation; the method thus has significant implications for privacy-preserving genome analytics.

Highlights

  • Personal genome sequences contain the information required for assessing genetic risks, matching genetic backgrounds between cases and controls in medical research, and detecting duplicate individuals or close relatives for medical, legal, or historical reasons

  • Our algorithm summarizes a personal genome as a “fingerprint” (Figure 1)

  • We developed a novel algorithm for computing “fingerprints” from genome data; the algorithm is akin to locality-sensitive hashing (Indyk and Motwani, 1998)

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Summary

Introduction

Personal genome sequences contain the information required for assessing genetic risks, matching genetic backgrounds between cases and controls in medical research, and detecting duplicate individuals or close relatives for medical, legal, or historical reasons. Research purposes served by personal genome sequencing include classifying individuals by population, reconstructing human history, assessing and controlling the quality of the sequence information itself, computing kinship matrices to support genome-wide association studies, and combining data sets for meta-analysis. Many of these applications involve comparison of two or more personal genomes. The recent UNICORN method enables independent mapping of individuals onto ancestry spaces based on detailed maps of minor allele frequency distributions (Bodea et al, 2016) These strategies offer better speed at the expense of limited applicability, severely reduced accuracy, or strong reliance on detailed prior knowledge about the population being studied

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