Sean is a bioinformatician in the Rahbari group where he integrates multi-omic single-cell data to study somatic mutations and cellular heterogeneity in healthy and cancer cells.
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So happy this paper is now out! was such a privilege getting to work on this project!
I am pleased to announce our latest paper.
We report results from single cell RNA and TCR sequencing, alongside spatial RNA and genome sequencing across different regions of kidney cancers:
https://www.cell.com/cancer-cell/fulltext/S1535-6108(22)00548-7
I’m super proud to show off my first lead paper, officially a real scientist now!!Thanks so much to @R_Rahbari and @drmatthewmurray for their guidance
Have a read if you’re interested in the role of small non-coding RNAs in germ cell tumours https://doi.org/10.1111/andr.13312
🗣️ Join us, @chiarabatini, @kayeshac1, @Cascade21, Maira Ihsan (@emblebi), @laidlawsean, @R_Rahbari, @CUSolomon, and @MaxGalder this November for our #NGS in #bioinformatics course.
🔗 Applications for this virtual event are open until 29 July 2022: https://www.ebi.ac.uk/training/events/genome-bioinformatics-resequencing-and-variant-calling-2022/ https://twitter.com/EBItraining/status/1524313351526002689
👀 Are you looking for a guide to the technology, analysis workflows, tools, and resources for #NGS data analysis?
Our virtual course, '#Genome #bioinformatics: #resequencing and variant calling', will provide just that!
🔗 Apply now: https://www.ebi.ac.uk/training/events/genome-bioinformatics-resequencing-and-variant-calling-2022/