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Introduction
Massively parallel DNA and RNA sequencing have become widely available, reducing the cost by several orders of magnitude and placing the capacity to generate gigabases to terabases of sequence data into the hands of individual investigators. These next-generation technologies have the potential to dramatically accelerate biological and biomedical research by enabling the comprehensive analysis of genomes and transcriptomes to become inexpensive, routine and widespread. The exploding volume of data has spurred the development of novel algorithmic approaches for primary analyses of sequence data in such areas as error correction, de novo genome assembly, novel transcript discovery, virus quasispecies assembly, etc. This workshop will bring together specialists to discuss the various mathematical and computational challenges presented by next-generation sequencing technologies.
Call for paper

Submission Topics

Workshop topics of interest include but are not limited to: · NGS error correction · Read mapping · Variant detection and genotyping · Characterization of structural variants · De novo genome and transcriptome assembly · Hap
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Important Date
  • Conference Date

    Jun 02

    2014

    to

    Jun 04

    2014

  • Jun 04 2014

    Registration deadline

Sponsored By
IEEE Computer Society
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