A Rapid Molecular Approach for Chromosomal Phasing

John F. Regan(Bio-Rad (United States)), Nolan Kamitaki(Harvard University), Tina C. Legler(Bio-Rad (United States)), Samantha Cooper(Bio-Rad (United States)), Niels Klitgord(Bio-Rad (United States)), George Karlin‐Neumann(Bio-Rad (United States)), Tsz Wai Catherine Wong(Harvard University), Shawn P. Hodges(Bio-Rad (United States)), Ryan Koehler(Bio-Rad (United States)), Svilen Tzonev(Bio-Rad (United States)), Steven A. McCarroll(Stanley Center for Psychiatric Research)
PLoS ONE
March 4, 2015
Cited by 76Open Access
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Abstract

Determining the chromosomal phase of pairs of sequence variants - the arrangement of specific alleles as haplotypes - is a routine challenge in molecular genetics. Here we describe Drop-Phase, a molecular method for quickly ascertaining the phase of pairs of DNA sequence variants (separated by 1-200 kb) without cloning or manual single-molecule dilution. In each Drop-Phase reaction, genomic DNA segments are isolated in tens of thousands of nanoliter-sized droplets together with allele-specific fluorescence probes, in a single reaction well. Physically linked alleles partition into the same droplets, revealing their chromosomal phase in the co-distribution of fluorophores across droplets. We demonstrated the accuracy of this method by phasing members of trios (revealing 100% concordance with inheritance information), and demonstrate a common clinical application by phasing CFTR alleles at genomic distances of 11-116 kb in the genomes of cystic fibrosis patients. Drop-Phase is rapid (requiring less than 4 hours), scalable (to hundreds of samples), and effective at long genomic distances (200 kb).


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