Unknown

Dataset Information

0

Ultrafast Comparison of Personal Genomes via Precomputed Genome Fingerprints.


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 ?s 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.

SUBMITTER: Glusman G 

PROVIDER: S-EPMC5623000 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

altmetric image

Publications

Ultrafast Comparison of Personal Genomes via Precomputed Genome Fingerprints.

Glusman Gustavo G   Mauldin Denise E DE   Hood Leroy E LE   Robinson Max M  

Frontiers in genetics 20170926


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 fi  ...[more]

Similar Datasets

| S-EPMC3556337 | biostudies-literature
| S-EPMC7385432 | biostudies-literature
| S-EPMC3232370 | biostudies-literature
| S-EPMC5057367 | biostudies-literature
| S-EPMC3587605 | biostudies-literature
| S-EPMC5123046 | biostudies-literature
| S-EPMC4678817 | biostudies-literature
| S-EPMC333770 | biostudies-other
| S-EPMC5645203 | biostudies-literature
| S-EPMC293463 | biostudies-literature