Skip to main content
Premium Trial:

Request an Annual Quote

ABI to Acquire Agencourt Personal Genomics for $120M, Plans Early-Access Placements in '07

NEW YORK, May 30 (GenomeWeb News) - Applied Biosystems plans to acquire Agencourt Personal Genomics for approximately $120 million in cash, ABI said today.

 

As part of the deal, Beckman Coulter will sell to ABI its minority interest in APG for approximately $50 million in cash. Beckman acquired a 49-percent stake in APG as part of its May 2005 acquisition of Agencourt Biosciences.

 

APG's massively parallel sequencing method, based on fluorescence stepwise ligation technology, is expected to complement current ABI platforms and will be applicable to genetic analysis applications such as de novo genome sequencing and high-throughput genotyping. ABI said that it expects to place initial systems with early-access customers in 2007.

 

APG's R&D team will continue to be based in Beverly, Mass., and will become part of ABI's molecular and cell biology division in Foster City, Calif.

 

The acquisition is expected to close in the third quarter, ABI and Beckman said.

 

ABI said that it expects the acquisition to be dilutive in both fiscal 2007 and 2008, primarily due to R&D spending, commercialization activities, and acquisition-related amortization associated.

 

ABI in October 2005 bought a stake in next-generation sequencing company Visigen and stressed one month later that it wasn't done shopping.

The Scan

Suicidal Ideation-Linked Loci Identified Using Million Veteran Program Data

Researchers in PLOS Genetics identify risk variants within and across ancestry groups with a genome-wide association study involving veterans with or without a history of suicidal ideation.

Algorithm Teases Out Genetic Ancestry in Individuals at Biobank Scale

Researchers develop an algorithm known as Rye to tease apart ancestry fractions in admixed individuals at a biobank-scale, applying it to 488,221 UK Biobank participants in Nucleic Acids Research.

Multi-Ancestry Analysis Highlights Comparable Common Variants at Complex Trait-Linked Loci

Researchers in Nature Genetics examine common variants implicated in more than three dozen conditions, estimating genetic effect similarities across ancestry tracts in admixed individuals.

Sick Newborns Selected for WGS With Automated Pipeline

Researchers successfully prioritized infants with potential Mendelian conditions for whole-genome sequencing or rapid whole-genome sequencing, as they report in Genome Medicine.