Top Tweets for #bcb22
Jippi es ist wieder #barconventberlin wir freuen uns hier zu sein
#barconvent #barconventberlin #BCB2022 #barconventber #BCB22 https://t.co/5vkK5KHRf8

KOVAL will be exhibiting at the BCB trade show in Berlin, October 10-12. You'll find us at the DISCUS booth, 20A21, so stop and say hello to your favorite distiller!
#BCB2022 #BCB #BarConvent #BCB22 #BCBBerlin #Berlin #DISCUS
https://t.co/b4onyuOuVk

Multiple reports on TME structure at #BCB22, esp. by #spatialTranscriptomics. But what is cause and what is consequence (inc. tumour genetics)? Can we identify non-cell autonomous interactions without time series? All agreed tremendous opportunities & need for new tools. #BCB22_Q
Multiple reports at #BCB22 of limited mapping between genotypes & phenotypes in cancer. Is #plasticity an intrinsic property of human cells, or do somatic genetic changes cause plasticity? Are clonal dynamics therefore less important for defining disease biology? #BCB22_Q
Final talk of #BCB22 is by Andrew Roth discussing Spatial Omics: The Next
Frontier to Study Tumour
Heterogeneity

The penultimate talk of the meeting is by Agnieszka Geras presenting, Celloscope: A probabilistic model for marker-gene-driven cell type deconvolution in spatial transcriptomics data #BCB22

Opening the final session at #BCB22 is @NickyMcGranahan presenting, Harnessing whole genome sequencing (WGS) data to investigate immune infiltrate in cancer and beyond.

Final session #BCB22. @NickyMcGranahan explains his ExTRECT method to infer T-cell fraction from tumour WES/WGS (detects copy number deletions caused by VDJ rearrangements). https://t.co/WDhG1rg9pC
I find this such a clever & insightful idea. But hope Nicky will rename it T-Rex
Next up is Barbara Bravi presenting, An interpretable machine learning framework to model antigen immunogenicity and T-cell receptor specificity #BCB22

Next up is our very own @cgatenbee discussing our recent @NatureComms paper, An immune bottleneck at the outset of colorectal cancer. #AndersonLab @mathonco
More details here https://t.co/rYDv0O5ySu #BCB22

Next up is Itay Tirosh presenting, Pan-cancer analysis of intra-tumor heterogeneity #BCB22

.@tiroshlab calls the collection of gene expression programs a "meta-program". Analysis of large public datasets show same meta-programs recur across cancers. Echos the "Hallmarks of Cancer", also @ara_anderson's "meta-phenotypes" idea. Paper: https://t.co/THnf7p00bh #BCB22
Next @Mdnicholson3 on using lesion segregation https://t.co/f8xOHTRt4E data & stochastic maths model to probe transcription coupled repair dynamics, working with @mst_paralogue. #BCB22
Now is @Mdnicholson3 presenting, Characterising the stochastic dynamics of transcription coupled repair via lesion-phasing and mathematical modelling #BCB22

.@marcjwills_ next at #BCB22 discusses copy number alterations (CNAs) and underlying mutational processes in ovarian cancer. Preprint: https://t.co/qgU5qusY6k Marc reports frequent recurrent allele-specific losses/gains, rate of which depends on WGD status.
Next up is @marcjwills_ from @SohrabShah lab presenting, Evolutionary selection on copy number alterations at single cell resolution #BCB22

Next, the fantastic @gcaravagna discussing his unpublished work on the timing of immune escape in AML treated by bone marrow transplant. The foundation of Giulio's work is the suite of tools he has created to infer evo dynamics from seq data https://t.co/RtvP1nmNp1 #BCB22
Discussion at the end of Andrew's talk around challenges of phylogenetic methods for CNAs, which include unknown CNA rates, non-independence of CNA events & that measurements of mutation rates from patient data confounded by selection. #BCB22
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