PHENOTIPS IS MOVING!
@phenotips is now the place for all things PhenoTips the #PrecisionMedicine software tool and company behind the it
@phenotipsOSS is the new hub exclusively for the open-source community, where you can gather and hear about updates
Hospital resources are under enormous strain, so we've made individual PhenoTips Cloud accounts #FREE until June 30th. Read more below about our pledge to support #genetics in this difficult time.
#gcchat#IamaGeneticCounselor#geneticcounselor#COVID19
https://t.co/mE2DY2CIHe
Join our CEO @orionbuske for The Alliance of International #Developers for #RareDiseases#Hackathon in #Kashiwa#Japan (1 hour away from #Tokyo)
Be part of a team of international developers working to address key challenges in #RareDisease diagnosis
https://t.co/HAyKgydrd6
Change is scary, so we’ve done our best to answer your questions. Huge thank you to our amazing PhenoTips open-source community for your invaluable contribution. None of this would've been possible without you.
#PrecisionMedicine#Genomics#Genetics
https://t.co/K6FKNUuYRe
The news is out!
Gene42 is now PhenoTips, we’ve got a new website https://t.co/YBiRHRqdHG, and we’re offering a brand new web-hosted #genomics software tool, PhenoTips Cloud.
These changes come at an exciting time for us, read all about it here:
https://t.co/fg9X6aoFib
Wishing you the very best during this festive season, #HappyHolidays from our team to yours!
Here we are at the @UofTStartup#ONRamp holiday party to get you in the spirit 🎄🤶🎅
#TBT to this interview in @nature of @PhenoTips founder Michael Brudno.
"The main goal is to help researchers find and group patients, search for genomic data on these individuals and explore the genes shared by patients with similar phenotypes."
https://t.co/Yb8s8QleLq
"#PrecisionMedicine puts insights [...] into practitioners’ hands via the software that they use every day to support the decisions they make as part of the patient care journey.”
Of which the integration of @PhenoTips into EHRs is a perfect example.
https://t.co/9wqL1Yk4EV
We are proud to work with @ConnectRD, providing @PhenoTips to simplify clinical data entry using the @hp_ontology. #RDConnect is a platform for #RareDisease research that facilitates data sharing and collaboration.
https://t.co/TrsNXg8Vuw
Dr. Knoppers, from @GA4GH, led the activation of a dormant right from the 1948 #UniversalDeclaration of #HumanRights that both protects and enables health data sharing, an incredibly important step towards innovation & the work we do #HumanRightsDay
https://t.co/wiVRbFeAPl
A shout out to the #Canadian#raredisease repository, #Genomics4RD based on @PhenoTips software & built by @gene42inc. Great example of how industry & academia can work together to push the needle towards faster diagnosis & greater efficiency in #healthcare. #ONGenomics2019