Skip to main content
Premium Trial:

Request an Annual Quote

New Products: Oxford Gene Technology's CytoSure ISCA+SNP Array; Scienion's SciReader CL

Premium

Oxford Gene Technology this week launched its CytoSure ISCA +SNP Array. Agilent Technologies manufactures the chip. Four, 180,000-marker arrays are printed on each slide.

OGT said its new array combines array comparative genomic hybridization probes, endorsed by the International Standards for Cytogenomic Arrays Consortium, with validated SNP content that allows users to detect copy number changes and loss of heterozygosity. The array includes content designed to focus on disease and syndrome-associated regions, in addition to offering whole-genome coverage.

OGT provides all users of its CytoSure arrays with its CytoSure Interpret Software.


Scienion this week introduced its SciReader CL array imaging platform. SciReader CL enables the colorimetric detection of multiplex assays and is suitable for all kinds of multiplex assays in planar array formats such as microtiter plates and slides, according to the Berlin-based firm. Image acquisition and analysis software are also optimized for 96-well formats.

SciReader comes with software and multiple features, including automated spot finding and evaluation of single arrays or array batches. It also allows for customization of array analysis and report formats. Ready to use applications include DNA and protein multi-parameter analysis, genotyping and pathogen identification, the firm said.

The Scan

Study Tracks Off-Target Gene Edits Linked to Epigenetic Features

Using machine learning, researchers characterize in BMC Genomics the potential off-target effects of 19 computed or experimentally determined epigenetic features during CRISPR-Cas9 editing.

Coronary Artery Disease Risk Loci, Candidate Genes Identified in GWAS Meta-Analysis

A GWAS in Nature Genetics of nearly 1.4 million coronary artery disease cases and controls focused in on more than 200 candidate causal genes, including the cell motility-related myosin gene MYO9B.

Multiple Sclerosis Contributors Found in Proteome-Wide Association Study

With a combination of genome-wide association and brain proteome data, researchers in the Annals of Clinical and Translational Neurology tracked down dozens of potential multiple sclerosis risk proteins.

Quality Improvement Study Compares Molecular Tumor Boards, Central Consensus Recommendations

With 50 simulated cancer cases, researchers in JAMA Network Open compared molecular tumor board recommendations with central consensus plans at a dozen centers in Japan.