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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Multidisciplinary and multi-omics molecular characterisation of rare cancers

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Nuria Lopez-Bigas @nlbigas·

24 Juin

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·

2 Juin

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·

2 Juin

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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NET Research Foundation @CureNETs·

21 Mai

@TalyaDayton's presentation of @CureNETs funded research from @HansClevers lab at @_Hubrecht won Presidential Award for Basic Science at #ENETS20 for their work on #NETCancer #organoids #tumoroids. Learn about this promising cell line. http://ow.ly/hVui50zMvKE

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Matthew Meyerson @meyersonlab·

25 Avr

1) Online today: our article on loss of heterozygosity (LOH) in ileal neuroendocrine tumors (NETs). https://onlinelibrary.wiley.com/doi/epdf/10.1002/gcc.22850
In this study, PhD student Zhouwei Zhang and colleagues address whether there is a germline basis for chromosome 18 LOH in these tumors.

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