Valentina Cipriani
148 posts
Valentina Cipriani
@Val3Cipriani
I (P-)value diversity. Senior Lecturer in Statistical Genomics @QMULWHRI Mendelian & Complex Diseases. Enthusiastic cyclist & Londoner. European.
London, England Katılım Mart 2019
399 Takip Edilen232 Takipçiler
@mnweedon What's the exact address for the meeting please? Thanks
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Truly collaborative science will always be acknowledged and stay the best 🙌🙌🙌 Very happy for you and your team!!!
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Valentina Cipriani retweetledi
We are hosting the South of England Genetic Epidemiology Group (SEGEG) meeting at the University of Exeter on July 1st!
Registration is free and now open - forms.office.com/e/tengc4eKLk
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Valentina Cipriani retweetledi
#ESHG2024
Any #bioinformaticians interested in joining my lab in Cape Town? #postdoc position available- benefit real ppl with #RareDiseases, work on interesting datasets, and live in the most beautiful city in the world!
Pls get in touch! Open to international candidates.
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Look forward to the #genomes for #undiagnosed session at 10:30AM and delivering our talk on gene burden analysis of the #100KGP data!
Also so exciting to be at the #ESHG2024 with the whole team @WHRIPhenGeno @QMULWHRI @QMUL_C4TB @QMULBartsTheLon
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Big shout out to many #gecip, and beyond, contributors for their help with triaging and annotating such a varied multi-disease analysis! Really grateful and eager for more collaborations!
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📢 In time for Xmas!
📝 Our pre-print of large-scale gene burden analysis of #100KGP 🧬 @GenomicsEngland data
🧐 Check table S2 for novel strong #raredisease gene associations and turn them into many new molecular #diagnoses!
@SmedleyDamian
@letizia_ve
medrxiv.org/content/10.110…
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🙏 re-tweet or apply! We are #hiring!
📢📢A 3-year Research Fellow post in #genomics is available @UCLchildhealth with close links with @QMUL @dundeeuni to study the #genetics of #RareDisease bronchiectasis
** Deadline: 21 March 2023
👇👇👇
ucl.ac.uk/work-at-ucl/se…
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Valentina Cipriani retweetledi
Two of our lab's projects are finalists for the open data science prize, please vote for #N3C or @MonarchInit #raredisease #openscience #covid #omop #ontologies #teamscience #dataintegration #standards herox.com/dataworks @AMIAinformatics @biocurator @OHDSI @iscb
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📢#LGN2022 folks, please share your thoughts
Is there still a divide between #RareDisease and common #ComplexGenetics?
Thrilled to share my thoughts with you after lunch at the @LdnGeneNet annual meeting, before keynote rare disease speaker @KorbonitsL
@QMULWHRI @QMUL_C4TB
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Think quantitatively!
Common disorders are quantitative traits.
Fascinating talk by prof Robert Plomin at the #LGN2022 annual meeting @LdnGeneNet
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Valentina Cipriani retweetledi
The Mundlos lab has open postdoc positions in the field of gene regulation, lncRNAs and evolutionary genomics. Fantastic environment at the MPI for Molecular Genetics. nature.com/naturecareers/…
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Valentina Cipriani retweetledi
‼️Reminder‼️
ECRs are encouraged to submit abstracts for flash talks (3min) on genetics of #rareDiseases or #complexTraits. There will be prizes for the best talks!🏅💷
Send abstracts to londongeneticsnetwork@gmail.com. More info on our website londongeneticsnetwork.com/annualmeeting/
London Genetics Network@LdnGeneNet
🚨We are thrilled to announce the LGN annual meeting on 2nd Dec! LGN members, check your inbox to sign up for an event on the genetics of complex traits & rare diseases, including keynotes from Prof Marta Korbonits & Prof Robert Plomin. ECRs can submit abstracts for flash talks!
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🙏 re-tweet or apply!
📢📢A #DataScientist/#Bioinformatician post is available within @QMUL @SmedleyDamian's team to work on data from the @NIH - funded MorPhiC project (Molecular Phenotypes of Null Alleles in Cells)
** Deadline: 25 Nov
👇👇👇
qmul.ac.uk/jobs/vacancies…
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📢#RareDisease talks are now part of the annual meeting programme of the @LdnGeneNet, together with #CommonComplex genetics 🙌
Are you an ECR? You can submit an #abstract for flash talks - *prices* available! 🎉
Sign up for the event and check out the full programme below
👇
London Genetics Network@LdnGeneNet
🚨We are thrilled to announce the LGN annual meeting on 2nd Dec! LGN members, check your inbox to sign up for an event on the genetics of complex traits & rare diseases, including keynotes from Prof Marta Korbonits & Prof Robert Plomin. ECRs can submit abstracts for flash talks!
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