Tag - rare disease

Illumina unveils PromoterAI, a groundbreaking algorithm to accelerate insights for rare disease diagnosis

AI model trained on de-identified data from 57 million people

Largest ever DNA sequencing dataset on UK child development studies available

TLDR; The Value of Drugs for Rare Disease Indications May Be Higher Than You Think – Assets for Neurodevelopmental Disorders Alone May Be Worth Beyond USD $420B.

The Cheap Genome Is Not Enough – We Need an “Accurate and Good Genome”

Genomenon Raises $20M Series B Financing, Launching a New Era in AI-Powered Genomic Data

2021 – Precision Medicine linked with Genomic Medicine: A Work in Progress

Patient-Centric Rare Disease Genome Maps Join The Web

PacBio and UCLA Health Announce Research Collaboration for Whole Genome Sequencing in Rare Diseases

Illumina and Genetic Alliance Launch $120 Million Global Initiative to Increase Equity and Improve Outcomes for Families Impacted by Genetic Disease

HiberCell Expands Translational Oncology Toolbox by Acquiring Genuity Science, Inc.

Pacific Biosciences and RCIGM Announce its First Collaboration for Whole Genome Sequencing Research

Variantyx Secures $20M in Funding for Whole Genome Sequencing Methodology, Advanced Testing Method that Diagnoses Genetic Disorders

Congenica Completes $50m Series C Funding Round to Advance Clinical Genomic Analysis Software and Data Platform

Invitae and Pacific Biosciences Collaborate to Develop Whole Genome Sequencing-Based Assays for Pediatric Epilepsy Diagnostics

Life of a Clinical Geneticist: Dealing Often With Heartless Bureaucracy

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