| Literature DB >> 22649081 |
Heike Lindner1, Michael T Raissig, Christian Sailer, Hiroko Shimosato-Asano, Rémy Bruggmann, Ueli Grossniklaus.
Abstract
We present a generally applicable method allowing rapid identification of causal alleles in mutagenized genomes by next-generation sequencing. Currently used approaches rely on recovering homozygotes or extensive backcrossing. In contrast, SNP-ratio mapping allows rapid cloning of lethal and/or poorly transmitted mutations and second-site modifiers, which are often in complex genetic/transgenic backgrounds.Mesh:
Year: 2012 PMID: 22649081 PMCID: PMC3416015 DOI: 10.1534/genetics.112.141341
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562