<p>In this study, we analyzed a series of colorectal cancers using a new sequencing technology that sequences more than 200 microsatellite regions in parallel. With this technology, we evaluated mono-, di- , tri- and tetranucleotide repeats to provide a broad spectrum of microsatellite instability (MSI) events. This deep sequencing technology provides greater than 2000X coverage and eliminates the need for PCR amplification. Because every read corresponds to a single DNA molecule, we eliminated artifacts introduced by PCR that obscured true MSI events. Also included in our analysis is a new method for detection of somatic copy number changes in 83 cancer genes, with which we can infer chromosomal instability (CIN) status.</p>

Improved Detection and Identification of Microsatellite Instability Features in Colorectal Cancer

Efficient targeted resequencing of human germline and cancer genomes by oligonucleotide-selective sequencing

CRISPR–Cas9-targeted fragmentation and selective sequencing enable massively parallel microsatellite analysis

A programmable method for massively parallel targeted sequencing