Oberseminar Computational Genomics

Module IN2122

Lecturer Julien Gagneur

Room Seminar room 01.09.034

Time Wednesdays, 9:00 - 10:30

Timetable

Wed, Apr 19	Laura Martens	Epicardioid single-cell genomics uncovers principles of human epicardium biology in heart development and disease
Wed, May 3	Pedro Tomaz da Silva	Solving the transcriptome code by sequencing 500 million years of fungi evolution
Wed, May 17	Yanik Bruns	Identifying co-elution peptides in chimeric mass spectra
Wed, May 24	Eva Holtkamp	DeepRVAT - A deep-learning approach to study rare variant effects on human traits
Wed, May 31	Shubhankar Londhe	Functionally informed genotype-to-phenotype prediction in rare disease
Wed, Jun 7	Vicente Yépez	Integration of RNA-seq with genotypic and phenotypic data across multiple rare diseases leads to increase diagnostics within Solve-RD
Wed, Jun 28	Felix Brechtmann	Burden testing in SolveRD - A systematic analysis to identify links between rare phenotypes and genes
Tue, Jul 11	Vangelis Theodorakis	Harmonizing RNA-seq analyses across Germany
Thu, Jul 20	Xueqi Cao	Expression outliers identified from 3,760 hematologic malignancy transcriptomes reveal LRP1B as a novel biomarker for hairy cell leukemia variant
Wed, Aug 2	Raquel Romão	Detecting expression outliers in first and last exons
Wed, Aug 30	Xavier Hernandez Alias	Regulation of mRNA translation by protein-metabolite interactions
Wed, Sept 20	Florian Hölzlwimmer	Multi-tissue prediction of aberrant gene expression
Wed, Sept 27	Nils Wagner	Using developmental and evolutionary data as extra layers of information to improve splicing perdictions