Blueprint Genetics will attend the 13th Asia Pacific Conference on Human Genetics (APCHG) 2019 from November 7-9 held in Manila, Philippines.
More information on the program can be found on the APCHG 2019 website.
We will have three interesting posters on a range of topics from our Cardiology, Nephrology, and Ophthalmology disease categories with specific information on our coverage of difficult to sequence regions of genes associated with X-linked retinal dystrophy and autosomal dominant polycystic kidney disease.
- Improved Clinical Utility of Next Generation Sequencing Panel Testing in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
- RPGR-ORF15 sequencing improves diagnostic yield in patients with inherited retinal dystrophies
- Improved Mapping Quality and Coverage in Highly Homologous PKD1 Gene Enable High Diagnostic Yield in ADPKD