Helen Firth

[The DECIPHER Project @deciphergenomic]

This #RareDiseaseDay we’re highlighting how open data sharing supports diagnosis, research & families living with rare conditions.
Watch to find out how access to rare disease data can help families better understand their children’s rare conditions
@Unique_charity @GeneticAll_UK

[The DECIPHER Project @deciphergenomic]

Approved genetic drugs/therapies, from the @N1Collaborative, N1C Gene Registry are now displayed in DECIPHER on a new Therapies tab - available from gene pages and patient records.

[The DECIPHER Project @deciphergenomic]

Links to @Unique_charity single gene disorder guides are now displayed in DECIPHER on gene pages, therapies tabs and patient records #inclusion #informationforeveryone

[The DECIPHER Project @deciphergenomic]

I'm excited to be speaking at #FOGLondon this January.

Have a question you'd like me to answer during my session? Drop it in the comments or message me, I'd love to hear your thoughts.

Further information: https://t.co/PpLfaSPEhp

#FOGLondon #genomics #biodata

[Centre for Personalised Medicine, Oxford (+ bsky) @CPMOxford]

🎙️ Extra episode from the Centre for Personalised Medicine podcast!

We look back at the highlights for the CPM in 2024-25, and look forward to the next year.

🎧Listen:
Apple: https://t.co/rvlZ15F6vB
Spotify: https://t.co/vvSFAxQDJ6

[Helen Firth @HelenVFirth]

Super cool new feature in DECIPHER!

[The DECIPHER Project @deciphergenomic]

Links to ProtVar are now available from the protein browser which provide functional and structural annotations for missense variants #protein @emblebi

[The DECIPHER Project @deciphergenomic]

Mitochondrial gene predictive scores are now displayed on gene pages which indicate the observed depletion or enrichment of specific variants classes in @gnomad_project compared to a mitochondrial genome constraint model under neutrality selection @NicoleLake

[The DECIPHER Project @deciphergenomic]

ClinGen Variant Curation Expert Panel Recommendations are now displayed more clearly on gene pages and in the pathogenicity evidence interface, especially for genes with recommendations for more than one disease @ClinGenResource @TheACMG

[The DECIPHER Project @deciphergenomic]

The bespoke PubMed search on gene pages is now displayed in bold. This link opens a browser tab with a PubMed search displaying publications that include the gene of interest @NIH

[The DECIPHER Project @deciphergenomic]

Descriptive names for gene and protein predictive scores are now displayed on gene pages to assist in demystifying these scores and making them easier to understand.

[The DECIPHER Project @deciphergenomic]

18 additional @gnomad_project short tandem repeats are now displayed; 9 recently discovered and 9 which are not currently linked to rare diseases but have historically appeared in various catalogs as suspected disease-causing loci.

[James Fasham @JamesFasham]

Kym Boycott #ESHG2025

What is matchmaking
One? Two? Zero? sided

Why do we do it (see the photo below ☺️)

👍👍@deciphergenomics.bsky.social second largest contributor to MatchMaker Exchange

❓sadly, 94% of genematcher entries have no phenotype DECIPHER is much better

[The DECIPHER Project @deciphergenomic]

Cancer case frequency data compiled by the National Disease Registration Service from diagnostic laboratories in England is now displayed on the protein browser. Data is available for ~4,500 variants in 13 cancer susceptibility genes including BRCA1, BRCA2, MSH2, PTEN and SMAD4.

[The DECIPHER Project @deciphergenomic]

Human Developmental Cell Atlas (HDCA) expression data is now displayed. Expression is displayed in 12 sections of a 6-7 post-conception week human embryo, alongside a sagittal view which displays the region of the embryo represented by each section @HaniffaLab @Muzz_Haniffa

[Centre for Personalised Medicine, Oxford (+ bsky) @CPMOxford]

Come and join us @StAnnesCollege on Tuesday 29th April at 17:30 for an evening of talks on the discovery of ReNU syndrome, from the key people involved. Register here for your free place: https://t.co/ht5oJ7PpEi

[Unique @Unique_charity]

It's Undiagnosed Children’s Day! 🙌 🎈

Many families spend years searching for answers, living with the unknown, without a name for their child’s condition. Please consider sharing this post, taking part in a fundraiser, or donating to support SWAN UK’s work.

#SWANUK

[Centre for Personalised Medicine, Oxford (+ bsky) @CPMOxford]

We're so pleased to share the winners and finalists from our latest art competition, which focused on the theme of how personalised medicine affects our planet.
Huge thank you to everyone who entered and congratulations to the winners and finalists!
https://t.co/iQgBDgcmsr

[The DECIPHER Project @deciphergenomic]

Can you spare 5 minutes to help shape the future development of DECIPHER?
Your views are extremely important to us.

Please access our user survey here: https://t.co/Y84zPWSSGj

[Cat in the Hat 🐈‍⬛ 🎩 🇬🇧 @_CatintheHat]

CAN YOU HELP US REACH 5K TONIGHT?

If you think health & social care settings should have clean air and new PPE standards to better protect patients & staff from airborne infections, please sign the petition below:

✍🏻 https://t.co/Ie1c1HL1qP