Oberseminar Computational Genomics

Module IN2122

Lecturer Julien Gagneur

Room Seminar room 01.09.034

Time Wednesdays, 9:00 - 10:30

Timetable

Thu, Apr 18	Eva Holtkamp	Integration of variant annotations using deep set networks boosts rare variant association genetics
Thu, Apr 25	Vicente Yépez	Harmonized framework for RNA-seq-based rare disease diagnostics in a pan-continental consortium - Solve-RD
Wed, May 8	Alexander Karollus	Studying the zero-shot capabilities of DNA Language Models using nucleotide dependency maps
Wed, May 15	Yanik Bruns	De novo sequencing of multiple peptides in chimeric mass spectra.
Wed, June 5	Gihanna Galindez	Towards the prediction of higher-order RNA structures
Thu, June 20	Andrew Behrens	Scalable RNA-seq-based pipelines for harmonized human transcriptomics in GHGA
Wed, Jul 10	Ines Scheller	Benchmarking protein outlier detection on rare disease proteomics and genomic data
Thu, Jul 18	Shounak Chakraborty	Aberrant expression analysis in the MASTER pan-cancer dataset
Wed, Jul 24	Xavier Hernandez-Alias	Regulation of mRNA translation by protein-metabolite interactions
Wed, Aug 21	Nils Wagner	Improving tissue-specific splicing predictions
Wed, Aug 28	Florian Hölzlwimmer	Multi-tissue prediction of aberrant gene expression
Wed, Sept 4	Johannes Hingerl	Scooby: Multi-modal genomic profile prediction from sequence at the resolution of single cells
Wed, Sept 18	Daniela Klaproth-Andrade	De novo peptide sequencing to identify post-translationally modified peptides
Wed, Sept 25	Shubhankar Londhe	Is the normal quantile transform justified for rare variant association testing?