Fast forward genetics: mutation mapping and identification using next-generation sequencing and enrichment of bulk segregant pools
Ontology highlight
ABSTRACT: Phenotype-driven forward genetic experiments are among the most powerful approaches for linking biology and disease to genomic elements. Although widely used in a range of model organisms, positional cloning of causal variants is still a very laborious process. Here, we describe a novel universal approach, named fast forward genetics that combines traditional bulk segregant techniques with next-generation sequencing technology and targeted genomic enrichment, to dramatically improve the process of mapping and cloning multiple mutants in a single experiment. In a two-step procedure the mutation is first roughly mapped by ‘light’ sequencing of the bulk segregant pool, followed by genomic enrichment and deep-sequencing of the mutant pool for the linked genomic region. The latter step allows f
ORGANISM(S): Arabidopsis thaliana
SUBMITTER: Michal Mokry
PROVIDER: E-GEOD-24511 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
ACCESS DATA