Illumina’s constellation tech a star in Genedx pilot
Genedx LLC partnered with Illumina Inc. to test whether Illumina’s constellation map read technology could shed light on…
Genetic investigation of sinopulmonary diseases in Vietnam: seeking specific causes from non-specific symptoms | Orphanet Journal of Rare Diseases
O’Donnell AE. Bronchiectasis – a clinical review. N Engl J Med. 2022;387(6):533–45. Article PubMed Google Scholar Flume PA,…
From genotype to phenotype with 1,086 near telomere-to-telomere yeast genomes
Strain culture and DNA extraction We used a collection of S. cerevisiae isolates that were previously sequenced using…
Expanding PRRT2 Syndrome: A Case Study
A recent case study has delved into a Chinese family grappling with the complexities of infantile convulsion and…
The rise of consumer eugenics
In a recent interview with New York Times columnist Ross Douthat, Noor Siddiqui, founder of the Silicon Valley…
Longevity gene from supercentenarians offers hope for disease that causes rapid aging in children
Credit: Pixabay/CC0 Public Domain A new breakthrough in a rare genetic disease which causes children to age rapidly…
Massapequa couple seeks cure for daughter with rare genetic mutation
Madeline Norton was diagnosed with a rare genetic mutation, causing her family to change their outlook on life.…
Genetic variation and genome-enabled selection of white lupin for key seed quality traits | BMC Genomics
Foyer CH, Lam H-M, Nguyen HT, Siddique KHM, Varshney RK, Colmer TD, et al. Neglecting legumes has compromised…
Bacterial Transporter Hijacked for Genetic Expansion
In a groundbreaking study poised to revolutionize the field of synthetic biology and genetic code expansion, researchers have…
Integrating Proteomics with Global Genetic Meta-Analysis
Ankylosing Spondylitis (AS) is a debilitating, immune-mediated disease which causes inflammation of the joints between the vertebrae, leading…
What part of ‘autism is genetic’ doesn’t RFK Jr. understand?
My father has blue eyes, but I do not. Mine are a lovely green. My older son nevertheless…
Nabsys Highlights OhmX™ Platform’s Ability to Accurately Verify Structural Variants in Undiagnosed Disorders and Workflow Optimizations at American Society of Human Genetics (ASHG) 2025 Annual Meeting
Newswise — PROVIDENCE, R.I., Oct. 15, 2025 — Nabsys 2.0, LLC (Nabsys), a pioneer in electronic genome mapping…