Duke
Cancer Centers Look to New NGS-Based 'Frankenpanel' to Get Fast Info on Clinically Actionable Genes
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Memorial Sloan Kettering Cancer Center is among the first healthcare systems to implement the rapid sequencing assay, which can consolidate single-gene tests.
Genotype-Centered Screen Points to Unexpected Prevalence of Heart Condition-Related Mutations
Hereditary cardiac transthyretin amyloidosis-related mutations appeared in 0.1 percent of UK Biobank participants, with higher prevalence in African ancestry participants.
Dengue Virus Study IDs Mutation Linked to Attenuated Disease
Researchers identified a single amino acid change in a dengue virus type 2 strain from Tonga that led to reduced viremia in mammalian cells.
GenieUs Genomics Aims to Stratify ALS Patients Using Bioinformatics Platform, Long-Read Sequencing
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The Australian firm seeks to validate its DiGAP platform in a clinical study by categorizing ALS patients according to their most affected biological pathways.
The researchers built on prior work on a prognostic model of overall survival that relied only on clinical factors.