Emily Hodges
Faculty Member
Last active: 4/26/2017

Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencing.

Hodges E, Rooks M, Xuan Z, Bhattacharjee A, Benjamin Gordon D, Brizuela L, Richard McCombie W, Hannon GJ
Nat Protoc. 2009 4 (6): 960-74

PMID: 19478811 · PMCID: PMC2990409 · DOI:10.1038/nprot.2009.68

Complementary techniques that deepen information content and minimize reagent costs are required to realize the full potential of massively parallel sequencing. Here, we describe a resequencing approach that directs focus to genomic regions of high interest by combining hybridization-based purification of multi-megabase regions with sequencing on the Illumina Genome Analyzer (GA). The capture matrix is created by a microarray on which probes can be programmed as desired to target any non-repeat portion of the genome, while the method requires only a basic familiarity with microarray hybridization. We present a detailed protocol suitable for 1-2 microg of input genomic DNA and highlight key design tips in which high specificity (>65% of reads stem from enriched exons) and high sensitivity (98% targeted base pair coverage) can be achieved. We have successfully applied this to the enrichment of coding regions, in both human and mouse, ranging from 0.5 to 4 Mb in length. From genomic DNA library production to base-called sequences, this procedure takes approximately 9-10 d inclusive of array captures and one Illumina flow cell run.

MeSH Terms (13)

Animals Base Sequence DNA Primers Gene Library Genomics Genomics Humans Mice Nucleic Acid Hybridization Oligonucleotide Array Sequence Analysis Polymerase Chain Reaction Sensitivity and Specificity Sequence Analysis, DNA

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