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RD-Connect

@ConnectRD

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An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research

Europe
Joined February 2013
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@ConnectRD
RD-Connect
7 years
What is RD-Connect and how does it advance research on #RareDiseases? Watch our explanatory video
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@ConnectRD
RD-Connect
5 months
RT @Solve_RD: The data infrastructure is the backbone of @Solve_RD 🔹 RD-Connect GPAP @ConnectRD to collect & analyse 🧬 data 🔹 @EGAarchive t…
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@ConnectRD
RD-Connect
1 year
RT @cnag_eu: ⏰ At 04:10PM, don't miss the session: 👉"Integration of phenotypic and genomic data for the diagnosis of rare conditions" 👩‍🔬By…
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@ConnectRD
RD-Connect
2 years
Join RD colleagues from across Europe for this workshop led by Sergi Beltrán, @LeslieMatalonga and @SteveLaurie42 to find out how the free to use RD-Connect GPAP can help you rapidly diagnose your RD patients.
@ERDERA_org
ERDERA
2 years
Learn about the benefits of using the RD-Connect Genome-Phenome Analysis (GPAP) platform for rare-disease analysis through a FREE @ejprarediseases Webinar! 📍Online 📅28 June 2023 🚨No registration needed! ℹ️Eligibility & complementary information:
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@ConnectRD
RD-Connect
2 years
RT @Solve_RD: Solve-RD webinar on #Genomic data analysis using @ConnectRD GPAP by @LeslieMatalonga now online 👉 L…
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@ConnectRD
RD-Connect
2 years
We are extremely happy to announce the new Genomic Analysis interface with improved user experience and new features! 👉Check it out here: or learn more by joining the webinar organised by @Solve_RD! Wed, 12 April 2023 at 1-2pm CT
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@ConnectRD
RD-Connect
2 years
RT @Solve_RD: Solve-RD webinar on genomic data analysis using @ConnectRD GPAP by @LeslieMatalonga: learn how to navigate through the platfo…
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@ConnectRD
RD-Connect
2 years
RT @cnag_eu: The @ConnectRD GPAP, developed and hosted at @CNAGCRG, enables users to submit, share, analyse and interpret data contributing…
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@ConnectRD
RD-Connect
2 years
Great to see so many people with different areas of expertise working together simultaneously to find new diagnoses for rare disease patients and their families. @Solve_RD has been a great success in fostering collaboration in RD across Europe.
@Solve_RD
Solve-RD
2 years
🔛Our Solvathon kicks off @cnag_eu with 25 on-site +25 online participants trying to solve many #RareDisease cases by integrated omics analysis 👩🏽‍💻👨🏽‍💻🧬 @ConnectRD @vaym88 @gagneurlab @IonSynapse @ERNIthaca @ERN_RND @euro_nmd @EpiCARE_ERN @_ERNRITA @SteveLaurie42 @LeslieMatalonga
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@ConnectRD
RD-Connect
2 years
RT @EGAarchive: Get to know the @GA4GH #htsget implementation that enables @ConnectRD #GPAP users to visualize genomic alignments at the @E
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@ConnectRD
RD-Connect
2 years
RT @Solve_RD: Did you miss our Solve-RD Treatabolome webinar? Here is the recording 👉 Learn how the database can he…
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@ConnectRD
RD-Connect
3 years
RT @Solve_RD: Poster P13.050.D: Identification & characterisation of BMPR1A and SMAD4 germline variants in patients w/ colorectal adenomato…
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@ConnectRD
RD-Connect
3 years
RT @cnag_eu: Right now! Workshop W11 on European Reference Networks #ERN at #ESHG2022 @SteveLaurie42 giving an overview of the main #resea
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