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SNP-Ratio Mapping (SRM): Identifying Lethal Alleles and Mutations in Complex Genetic Backgrounds by Next-Generation Sequencing
Author(s) -
Heike Lindner,
Michael T. Raissig,
Christian Sailer,
Hiroko Shimosato-Asano,
Rémy Bruggmann,
Ueli Grossniklaus
Publication year - 2012
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.112.141341
Subject(s) - biology , genetics , allele , snp , dna sequencing , identification (biology) , cloning (programming) , genome , positional cloning , computational biology , backcrossing , mutation , gene , genotype , single nucleotide polymorphism , phenotype , programming language , botany , computer science
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.

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