février 2020 - Rare Cancers Genomics

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Lynnette Fernandez Cuesta and Matthieu Foll presented the Rare Cancer Genomics initiative at the International Symposium on Human Genomics – February 10-12, 2020 in Paris (France)

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Hilary Robbins @hilaryarobbins·

18 Nov

📢 Please RT! Come work with me as a #postdoc in lung cancer risk prediction at @IARCWHO in France.

Required skills: epidemiology, biostatistics, longitudinal data analysis. Experience in lung cancer, cancer screening, cost-effectiveness is a plus.

https://www.iarc.fr/wp-content/uploads/2020/11/PostDoc_GEP_lung_cancer_risk_prediction.pdf

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Charles Swanton @CharlesSwanton·

2 Sep

1/24 - Can we decipher order from cancer genomes? Our new paper “Pervasive chromosomal instability and karyotype order in tumour evolution” comes out in Nature today: https://www.nature.com/articles/s41586-020-2698-6 @BCRFcure @TheCrick @CRUKresearch @RosetreesT @uclcancer @SwantonLab @royalsociety

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GigaScience @GigaScience·

4 Nov

Accessing and reviewing Controlled Access Data of Rare Cancers. Q&A with @m_foll from @IARCWHO on new & reproducible work presenting multi-omic data from rare lung neuroendocrine neoplasms http://gigasciencejournal.com/blog/controlled-access-data/

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Jamie Blundell @jrblundell·

9 Oct

How many driver mutations in healthy tissues are missed by gene-focussed sequencing panels? How much driver mutation “dark matter” is there? @gladyspoon1 uses synonymous mutations, which act like naturally occurring barcodes, to tell us the answer…[1/7] https://www.biorxiv.org/content/10.1101/2020.10.08.331405v1

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Justo P. Castaño 🔬🧬🧫🧪#SinCienciaNoHayFuturo @JustoCastano·

29 Sep

Finalizó la Reunión de #GETNE Andalucía sobre tumores Neuroendocrinos #TNEs #NETs
GRACIAS a
🧑‍💼Todos los ponentes x sus presentaciones, didácticas e interesantes

Nuestros patrocinadores @adacap_news @NovartisSpain @IpsenGroup @pfizer_spain x su apoyo🙏
Y @GrupoGetne y @GrupoMfar

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