Simple scalable nucleotic FPGA based short read aligner for exhaustive search of substitution errors

With the advent of the new and continuously improving technologies, in a couple of years DNA sequencing can be as commonplace as a simple blood test. The growth of sequencing efficiency has a larger exponent than the Moore’s law of standard processors, hence alignment and further processing of seque...

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Bibliographic Details
Main Authors: Fehér Péter, Fülöp Ágnes, Debreczeni Gergely, Nagy-Egri Máté, Vesztergombi György
Format: Article
Language:English
Published: Sciendo 2015-12-01
Series:Acta Universitatis Sapientiae: Informatica
Subjects:
Online Access:https://doi.org/10.1515/ausi-2015-0017