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IP Roundup: Meso Scale Technologies, Fluidigm, Affymetrix, Luminex, Honeywell, Samsung Electronics


Title: Assay plates, reader systems and methods for luminescence test measurements.
Patent Number: 8,808,627
Filed: Nov. 11, 2010
Lead Inventor: Jacob Wohlstadter, Meso Scale Technologies

Title: Method and system for microfluidic device and imaging thereof.
Patent Number: 8,808,640
Filed: Jan. 31, 2013
Lead Inventor: Emerson Quan, Fluidigm

Title: Methods for genotyping selected polymorphism.
Patent Number: 8,808,995
Filed: Jan. 11, 2012
Lead Inventor: Ketih Jones, Affymetrix

Title: Method for immobilizing biologic molecules on solid surfaces.
Patent Number: 8,809,071
Filed: Nov. 29, 2002
Lead Inventor: Marcella Chiari

Title: Method for nucleic acids isolation.
Patent Number: 8,809,519
Filed: June 18, 2009
Lead Inventor: Jesus Ching, Luminex

Title: Microarray reader based on evanescent wave detection.
Patent Number: 8,809,810
Filed: May 20, 2010
Lead Inventor: Xuanbin Liu, Honeywell International

Title: Method, medium, and system for encrypting and/or decrypting information of microarray.
Patent Number: 8,811,610
Filed: Sept. 17, 2008
Lead Inventor: Taejin Ahn, Samsung Electronics

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.