A pipeline for local assembly of minisatellite alleles from single-molecule sequencing data
Author(s) -
Denye Ogeh,
Richard M. Badge
Publication year - 2016
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btw687
Subject(s) - sequence assembly , minisatellite , biology , sanger sequencing , computational biology , dna sequencing , genetics , human genome , genome , massive parallel sequencing , hybrid genome assembly , reference genome , allele , dna , gene , microsatellite , gene expression , transcriptome
The advent of Next Generation Sequencing (NGS) has led to the generation of enormous volumes of short read sequence data, cheaply and in reasonable time scales. Nevertheless, the quality of genome assemblies generated using NGS technologies has been greatly affected, compared to those generated using Sanger DNA sequencing. This is largely due to the inability of short read sequence data to scaffold repetitive structures, creating gaps, inversions and rearrangements and resulting in assemblies that are, at best, draft forms. Third generation single-molecule sequencing (SMS) technologies (e.g. Pacific Biosciences Single Molecule Real Time (SMRT) system) address this challenge by generating sequences with increased read lengths, offering the prospect to better recover these complex repetitive structures, concomitantly improving assembly quality.
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