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? |