GateKeeper: a new hardware architecture for accelerating pre-alignment in DNA short read mapping

Date

2017-11-01

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Alser, M.
Hassan, H.
Xin, H.
Ergin, O.
Mutlu, O.
Alkan C.

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Abstract

High throughput DNA sequencing (HTS) technologies generate an excessive number of small DNA segments -called short reads- that cause significant computational burden. To analyze the entire genome, each of the billions of short reads must be mapped to a reference genome based on the similarity between a read and ‘candidate’ locations in that reference genome. The similarity measurement, called alignment, formulated as an approximate string matching problem, is the computational bottleneck because: (i) it is implemented using quadratic-time dynamic programming algorithms and (ii) the majority of candidate locations in the reference genome do not align with a given read due to high dissimilarity. Calculating the alignment of such incorrect candidate locations consumes an overwhelming majority of a modern read mapper’s execution time. Therefore, it is crucial to develop a fast and effective filter that can detect incorrect candidate locations and eliminate them before invoking computationally costly alignment algorithms.

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Bioinformatics

Publisher

Oxford University Press

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Published Version (Please cite this version)

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English