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Archives des Non classé - Rare Cancers Genomics

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By RCG
14 février 2020

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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Alex Di Genova @digenoma·

They demonstrate that evolutionary genomic measures (dN/dS) can predict clinical response to immunotherapy. Nice work of my friend @LuisglsZ https://twitter.com/biorxivpreprint/status/1286082330315169793

bioRxiv@biorxivpreprint

dN/dS dynamics quantify tumour immunogenicity and predict response to immunotherapy https://biorxiv.org/cgi/content/short/2020.07.21.215038v1 #bioRxiv

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Muin J. Khoury @MuinJKhoury·

Genomics has a robust culture of data sharing. Data sharing anchors reproducible science, but expectations and best practices are often nebulous. Excellent @NatureRevGenet review. https://www.nature.com/articles/s41576-020-0257-5

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Nuria Lopez-Bigas @nlbigas·

Just out in @nature one of the most interesting discoveries I have had the privilege to witness and participate

Pervasive lesion segregation shapes cancer genome evolution.

https://rdcu.be/b49w4

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Lior Pachter @lpachter·

Haven't been able to work much but took a moment to read https://nature.com/articles/s41592-020-0854-4. Cool to see they agreed w/ us that "using transcript-level..[for] gene expression analyses in #scRNASeq..reveal[s] subtle differences across cell populations that would otherwise be left undetected"

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paoloditommaso @PaoloDiTommaso·

I’m very excited to announce the release of Tower Launch for AWS Batch and Google Cloud LifeSciences along with a bunch of new features! Deployment of Nextflow pipelines couldn't be easier! 🎉🎉
https://seqera.io/blog/tower-cloud-launch/

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Multidisciplinary and multi-omics molecular characterisation of rare cancers

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