[작성자:] cms3billion
-
Introduction to 3billion’s Genomic Testing Services
Join us for an insightful webinar where you can learn all about 3billion’s services in one go. What content does the webinar cover?– An overview of our services and comparisons– A step-by-step guide to using our services– The unique advantages of 3billion’s services– Real case examples showcasing our impact How can I watch it?Click the…
-
Rethinking Clinical Practice for Rare Neurodevelopmental Disorders in the Genomic Era
Webinar at the 10th Alexandria Pediatric Neurology Conference Speaker: Dr. Hane Lee, Chief Genomics Officer (CGO) of 3billion 3billion’s Chief Genomics Officer, Dr. Hane Lee, presented as a speaker at the Annual Alexandria Pediatric Neurology Conference. The Annual Alexandria Pediatric Neurology Conference was held in collaboration with Child Neurology Society and the British Paediatric Neurology Association. Dr.…
-
Practical Paediatrics Update 2022
EMERGING TRENDS IN PAEDIATRIC CARE Clinical Practice for Rare Genetic Disease in Genomic Era Go Hun Seo MD, Ph.D. (Chief Medical Officer of 3billion) In this talk, Go Hun Seo introduced the CAP (College of American Pathologists)-accredited genomic sequencing tests that 3billion currently offers and talked about the bioinformatics pipeline and variant interpretation tool, EVIDENCE,…
-
Pediatric Diagnostic Odysseys: Exome Success Stories in Arab Countries
In this webinar, with a clinical genetic expert from 3billion and pediatricians from Egypt, get insights into the use of genetic testing in pediatrics with examples. What content does the webinar cover?– Types and characteristics of genetic tests that can be used in clinical practice– Why genetic testing is useful, especially in pediatrics– Diagnostic cases…
-
How 3billion’s WES Overcomes Exome Sequencing Limitations
Exome sequencing (ES) has established itself as a pivotal tool in molecular diagnostics due to its cost-effectiveness and ability to identify pathogenic variants within coding exons, where approximately 80% of reported pathogenic variants reside. Despite its advantages, ES faces several limitations. Limitations of Standard Exome Sequencing For a more detailed exploration of the limitations of…
-
The Importance and Evolution of Informed Consent
Informed consent has been officially around for over half a century with its first legal discussion beginning in 1905 and its establishment by law in 19571. Whether this sounds young or old, the advances and spread of modern medicine and research have undoubtedly made informed consent now a universal principle of medical and research ethics.…
-
Global rare disease diagnosis cooperation using ClinVar
What is ClinVar? ClinVar is a public database operated by the U.S.A. National Institutes of Health (N.I.H.), in which information about variants associated with human phenotypic information is saved. Since the celebration of the submission of a million cases by 73 countries in 2019, as of Aug. 3rd, 2022, more than 2.3 million cases have…