RT Journal Article SR Electronic T1 CRISPR-directed mitotic recombination enables genetic mapping without crosses JF bioRxiv FD Cold Spring Harbor Laboratory SP 040428 DO 10.1101/040428 A1 Meru J. Sadhu A1 Joshua S. Bloom A1 Laura Day A1 Leonid Kruglyak YR 2016 UL http://biorxiv.org/content/early/2016/04/27/040428.abstract AB Linkage and association studies have mapped thousands of genomic regions that contribute to phenotypic variation, but narrowing these regions to the underlying causal genes and variants has proven much more challenging. Resolution of genetic mapping is limited by the recombination rate. We developed a method that uses CRISPR to build mapping panels with targeted recombination events. We tested the method by generating a panel with recombination events spaced along a yeast chromosome arm, mapping trait variation, and then targeting a high density of recombination events to the region of interest. Using this approach, we fine-mapped manganese sensitivity to a single polymorphism in the transporter Pmr1. Targeting recombination events to regions of interest allows us to rapidly and systematically identify causal variants underlying trait differences.