Mutation detection with next-generation resequencing through a mediator genome.
Ontology highlight
ABSTRACT: The affordability of next generation sequencing (NGS) is transforming the field of mutation analysis in bacteria. The genetic basis for phenotype alteration can be identified directly by sequencing the entire genome of the mutant and comparing it to the wild-type (WT) genome, thus identifying acquired mutations. A major limitation for this approach is the need for an a-priori sequenced reference genome for the WT organism, as the short reads of most current NGS approaches usually prohibit de-novo genome assembly. To overcome this limitation we propose a general framework that utilizes the genome of relative organisms as mediators for comparing WT and mutant bacteria. Under this framework, both mutant and WT genomes are sequenced with NGS, and the short sequencing reads are mapped to the me
SUBMITTER: Wurtzel O
PROVIDER: S-EPMC3013116 | biostudies-literature | 2010 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA