| Literature DB >> 27938323 |
Michael Giolai1, Pirita Paajanen1, Walter Verweij1, Lawrence Percival-Alwyn1, David Baker1, Kamil Witek2, Florian Jupe2,3, Glenn Bryan4, Ingo Hein4, Jonathan D G Jones2, Matthew D Clark1,5.
Abstract
Targeted capture provides an efficient and sensitive means for sequencing specific genomic regions in a high-throughput manner. To date, this method has mostly been used to capture exons from the genome (the exome) using short insert libraries and short-read sequencing technology, enabling the identification of genetic variants or new members of large gene families. Sequencing larger molecules results in the capture of whole genes, including intronic and intergenic sequences that are typically more polymorphic and allow the resolution of the gene structure of homologous genes, which are often clustered together on the chromosome. Here, we describe an improved method for the capture and single-molecule sequencing of DNA molecules as large as 7 kb by means of size selection and optimized PCR conditions. Our approach can be used to capture, sequence, and distinguish between similar members of the NB-LRR gene family-key genes in plant immune systems.Keywords: NB-LRR gene; PacBio; RenSeq; gene enrichment; resistance gene; targeted capture
Mesh:
Substances:
Year: 2016 PMID: 27938323 DOI: 10.2144/000114484
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993