Skip to main content
Premium Trial:

Request an Annual Quote

Illumina Acquires HLA Typing Solutions Company Conexio Genomics

NEW YORK (GenomeWeb) – Illumina announced today that it has acquired Australian HLA typing solutions provider Conexio Genomics.

Terms of the deal were not disclosed.

Illumina first partnered with Conexio in March 2015 to offer the TruSight HLA Solution, a sequencing-based product for accurate HLA typing across thousands of known and novel HLA alleles. The product uses Conexio's Assign software for analysis and reporting.

The acquisition will enable Illumina to develop NGS-based transplant diagnostics assays, including a new solution for interrogating genomic variants in the gamma genomic block of the major histocompatibility complex, the company said in a statement.

"The addition of Conexio products and people solidify our HLA capabilities and demonstrate Illumina's ongoing commitment to HLA and ultimately to the field of transplant science," Alex Lindell, Illumina's associate director of market development for HLA, said in the statement.

Conexio's NGS development programs will be folded into Illumina's existing business units.

The Scan

Positive Framing of Genetic Studies Can Spark Mistrust Among Underrepresented Groups

Researchers in Human Genetics and Genomics Advances report that how researchers describe genomic studies may alienate potential participants.

Small Study of Gene Editing to Treat Sickle Cell Disease

In a Novartis-sponsored study in the New England Journal of Medicine, researchers found that a CRISPR-Cas9-based treatment targeting promoters of genes encoding fetal hemoglobin could reduce disease symptoms.

Gut Microbiome Changes Appear in Infants Before They Develop Eczema, Study Finds

Researchers report in mSystems that infants experienced an enrichment in Clostridium sensu stricto 1 and Finegoldia and a depletion of Bacteroides before developing eczema.

Acute Myeloid Leukemia Treatment Specificity Enhanced With Stem Cell Editing

A study in Nature suggests epitope editing in donor stem cells prior to bone marrow transplants can stave off toxicity when targeting acute myeloid leukemia with immunotherapy.