May 25th is Huntington Awareness Day ๐
Iโve added early HTT gene support to Gene Exon Editor, with a slider
to explore CAG repeat changes visually.
Try the WIP version:
https://t.co/Jxu6t5oOi0
Feedback welcome.
#LetsTalkAboutHD#HuntingtonsDisease
Happy World DNA Day! ๐งฌ
Decoding DNA โก๏ธ mRNA โก๏ธ Protein shouldn't be a mystery. I built DNAGCat to help #RareDisease families learn the science of genetics through play! ๐
Empower your journey and play today:๐ https://t.co/YVJB7vIDIc
#WorldDNADay#Genetics#STEM#BioTech#DNA
What if AI could invent enzymes that nature hasnโt seen? ๐ฉโ๐ฌ๐งโ๐ฌ
Introducing ๐ชฉ DISCO: Diffusion for Sequence-structure CO-design
14 rounds of directed evolution and over a year of wet lab work. That's what it took to engineer an enzyme for selective C(spยณ)โH insertion, one of the most challenging transformations in organic chemistry.
DISCO surpasses this with a single plate. No pre-specified catalytic residues, no template, no theozyme, no inverse folding, just joint diffusion over protein sequence and structure.
๐ Blog: https://t.co/j9Za0JigfO
๐ Paper: https://t.co/ficrYNBBrM
๐ป Code: https://t.co/p81sSwoaPH
This is another WIP - Rare Disease Planet - allow families to place their location on the map, and also add in current medical trials they are on for their particular rare disease ( Huntingtons, DMD etc ), and get a global view of potential treatment in other parts of the world.
Hereโs a sneak keep at one of a new WIP app, allowing families to become more familiar with chromosomes and genes ( where their gene is located, where other genes for things like eye colour are located - what other genes are located on the chromosome etc )
Itโs Rare Disease Day 2026. ๐
Iโm a rare disease dad building FREE web apps to support families, patients & advocates.
No paywalls. Just tools that help.
Explore & share ๐ https://t.co/WGws0n2GK6โจ#RareDiseaseDay#MakeRareVisible#RareDisease
Two sneak peeks at switching between multiple related genes, live now for testing but not unlocked yet in public UI
SGCA/B/D/G
https://t.co/PioSync11w
OCA1/2/3/4
https://t.co/e8c2m7ZI0w
#raredisease#RareDiseaseDay#exon
Some rare diseases have multiple associated genes - latest development build allows you to pick multiple genes and easily switch between them using tabs ( in this case, SGCA/B/D/G )
Navigating a rare disease? You're not alone. ๐ Just 1 week until #RareDiseaseDay! We've launched Rare Disease Appsโ100% FREE tools to map & compare your medical journey. You stay in total control of your data.
Watch below! ๐ https://t.co/yr7dtAMj3U
Adding in group label support to the Exon Editor, as part of supporting other genes
@Lovable@lovableshipped@rarediseaseday@RareDiseases
Check out other free rare disease apps in development atโฆ
https://t.co/yr7dtAMj3U
๐ 2 weeks to @RareDiseaseDay (Feb 28).
As a parent, a hard part of a rare diagnosis is feeling alone.
I built Shared Footsteps so families can map & compare medical timelines.
https://t.co/yr7dtAMj3U
Opt in/out anytime. GDPR/Privacy first.
Please try it. Invite others. ๐