Friedreich's Ataxia (FA) Awareness Day
In recognition of Friedreich's Ataxia (FA) Awareness Day, 21 May 2022, we welcome Alex Fielding to talk about his experience of this rare disease.
Unlocking sociocultural and community factors for the global adoption of genomic medicine
Dr Charles Steward PAE lead at Congenica talks about his latest article published in the Orphanet Journal of Rare Diseases
Congenica wins Technology Company of the Year
Congenica wins Technology Company of the Year at the 2022 Cambridge Independent Science and Technology Awards
Discovering Primary Ciliary Dyskinesia (PCD)
Fiona Copeland is mother of two boys with the same rare disease, PCD, but had to wait six years for a genetic diagnosis. Here she shares her story of discovering Primary Ciliary Dyskinesia (PCD).
Congenica Appoints Dr. Tom Barber as Chief Scientific Officer
Congenica appoints Dr. Tom Barber as Chief Scientific Officer to lead the development and delivery of Congenica’s scientific and clinical vision
The Hong Kong Genome Project: Benefits to Patients
Mr. K. P. Tsang, Chairman of Rare Disease Hong Kong, talks about the benefits to patients of the Hong Kong Genome Project.
Congenica 为香港基因组计划提供全基因组测序三级数据分析
康剑尼科(Congenica)是一家数字健康公司，助力快速准确解读复杂基因组数据，为患者提供改变一生的答案。公司于今天宣布其将为香港首个大型基因组测序计划「香港基因组计划」提供全基因组测序三级数据分析。
Congenica to provide Tertiary Analysis for Whole Genome Sequencing for Hong Kong Genome Project
Congenica selected to provide tertiary analysis for whole genome sequencing services for the Hong Kong Genome Project (HKGP).
Rare Disease Framework Action Plan for England
Andrea Haworth, Lead Clinical Scientist Rare Disease, comments on the Rare Diseases Action Plan, launched in England to coincide with Rare Disease Day.
Susannah’s Diagnostic Odyssey
For Rare Disease Day, we interview Luke Rosen and his daughter Susannah’s physician, Wendy Chung about their journey to diagnosis of rare disease KIF1A.
Insights into Rare Disease from the Congenica Team
We work to improve the lives of people living with rare and inherited diseases. Here, some of our team talk about what rare disease means to them.
From Lung Collapse to Ironman
Lea has BHD and shares her empowering story with us for Rare Disease Day. See Lea's inspirational journey from lung collapse to Ironman in this video.