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Latest 2022 news articles, blog posts & updates from industry experts
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Study uncovers mechanisms underlying microglia-driven neuroinflammation in Alzheimer's disease 
Study identifies how three novel genes cause neurodevelopmental disorders 
Personalis, Tempus Partner to Commercialize Blood-Based Minimal Residual Disease Test 
Thermo Fisher Scientific, Pfizer Canada Grant C$300K to Study NGS in Colorectal Cancer Care 
Inferring multi-locus selection in admixed populations 
Cancer Shredder Utilizes CRISPR, Targets Glioblastoma 
Nucleus RadioPharma: Building CDMO Sites to Ride the Radioligand Therapy Wave 
Quest Diagnostics, Scipher Medicine Collaborate on Rheumatoid Arthritis Test 
Nvidia Looks to Genentech for Its Next Leap in AI Drug Discovery 
Lung Cancer May Be Halted by Tumor Suppressor Protein 
More Accurate Pediatric Neural Organoids Capture Features of the Cortex 
Fetal Exome Sequencing Studies Point to Noninvasive Prenatal Screening Applications 
Transfer learning with false negative control improves polygenic risk prediction 
An allele-sharing, moment-based estimator of global, population-specific and population-pair FST under a general model of population structure 
Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves 
Phosphate starvation decouples cell differentiation from DNA replication control in the dimorphic bacterium Caulobacter crescentus 
Infant face preference linked to genetics 
Quadram Institute Leads €1.1M Consortium Using Nanopore Sequencing for AMR Surveillance 
Molecular characterization of novel and rare DNA variants in patients with galactosemia 
What to know about brain aneurysm growth 
Hemochromatosis: Primary, secondary, and neonatal 
What does genetic testing for hypertrophic cardiomyopathy involve? 
Obesity linked to prostate cancer risk: New study uncovers inherited dangers from fathers 
Breakthrough decoding of the Y chromosome revolutionizes digestive disease research 
A comprehensive preimplantation genetic testing approach for SEA-type α-thalassemia by fluorescent gap-polymerase chain reaction combined with haplotype analysis 
Association of SDF-1 and its receptor CXCR4 polymorphisms on the susceptibility of diabetic retinopathy in the Taiwanese population 
Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 
Expanding the phenotype and metabolic basis of ATP6AP2-congenital disorder of glycosylation in a Chinese patient with a novel variant c.185G>A (p.Gly62Glu) 
Heterozygous hemochromatosis: What to know 
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