Excited to attend #ISMB2026 next week and learn from great #ISCB computational biologists. Also, present my poster: Please stop by poster D-380, Track: #VarI: Variant Interpretation; July 16, 2026 at 10:00 - 11:00 and 16:00 - 16:40
Li et al. discovered a novel FOXG1(p.Tyr254Cys) variant that causes congenital male Rett syndrome in a 6-year-old. Also highlights microcephaly and intellectual disability as key clinical features of this condition.
https://t.co/Q4OUBYN6W1 #Rettsyndrome#FOXG1
Introducing VarViz: a free, open-source web app for interpreting missense variants.
Multiple interactive evidence tracks. Automated ACMG/AMP Tags. All in one protein-level view. https://t.co/bI94SYnfAv #genomics#variantinterpretation#ACMG#RareDiseases#bioinformatics