Publikationen von M. Vingron

Heber, S.; Stoye, J.; Frohme, M.; Hoheisel, J.; Vingron, M.: Resampling Methods in Physical Mapping. In: Classification, Automation, and New Media, S. 437 - 444. Proceedings of the 24th Annual Conference of the Gesellschaft für Klassifikation, University of Passau, 15. März 2000 - 17. März 2000. Springer-Verlag, Heidelberg (2002)

Huber, W.; von Heydebreck, A.; Gunawan, B.; Vingron, M.; Füzesi, L.; Poustka, A.; Sültmann, H.: Transcription profiling of renal cell carcinoma. Annual Meeting of the German Society for Pathology, Wien, 03. April 2002 - 06. April 2002., (2002)

Meinel, T.; Krause, A.; Stoye, J.; Schmidt, A.; Luz, H.; Vingron, M.: The SYSTERS Protein Family Webserver. In: European Conference on Computational Biology 2002 (ECCB 2002) in conjunction with the German Conference on Bioinformatics 2002 (GCB 2002), S. / - /. European Conference on Computational Biology 2002 (ECCB 2002), Congress Centrum Saar, Saarbrücken, 06. Oktober 2002 - 09. Oktober 2002. (2002)

von Heydebreck, A.; Huber, W.; Poustka, A.; Vingron, M.: Variance stabilization and robust normalization for microarray gene expression data. In: Proceedings in Computational Statistics, S. 623 - 628 (Hg. Härdle, W.; Rönz, B.). COMPSTAT 2002 - Proceedings in Computational Statistics - 15th Symposium, Berlin, 24. August 2002 - 28. August 2002. Physika Verlag, Heidelberg (2002)

Moeinzadeh, M.; Yang, J.; Vingron, M.: Haplotype reconstruction for polyploid organisms. BREW 2015: Bioinformatics Research and Education Workshop, University of Tartu, Tartu, Estonia (2015)

Moeinzadeh, M.; Yang, J.; Vingron, M.: Haplotype reconstruction for sweet potato (Ipomoea Batatas [L.] Lam). 19. International Conference on Research in Computational Molecular Biology (RECOMB 2015), Warsaw (2015)

Rosebrock, D.: Dissecting regional heterogeneity and modeling transcriptional cascades in brain organoids. Dissertation, vii, 129 S. (2023)

Bressin, A. S.: A Multi-Omics Analysis of Transcription Control by BRD4. Dissertation, ix, 205 S. (2023)

Ly, L.-H.: Deciphering cellular heterogeneity by single-cell transcriptome analysis. Dissertation, xiii, 131 S. (2022)

Kleinert, P.: Computational interpretation of disease-causing, structural, and non-coding human genetic variants. Dissertation, 118 S. (2022)

Gajos, M.: Analysis of the determinants of Pol II pausing. Dissertation, vi, 125 S. (2022)

Abdullaev, E.: Dynamical Aspects of the Evolution of Segmental Duplications in the Human Genome. Dissertation, xiii, 129 S. (2022)

Gralinska, E.: Association Plots visualize cluster-specific genes from high-dimensional transcriptomics data. Dissertation, vi, 108 S. (2022)

Barel, G.: Network Propagation with Node Core for Genotype-Phenotype Associations and Module Identification. Dissertation, xii, 161 S. (2021)

Zehnder, T.: Computational Approaches for the Prediction of Gene Regulatory Elements and the Analysis of their Evolutionary Conservation. Dissertation, vii, 155 S. (2021)

Heller, D.: Structural variant calling using third-generation sequencing data. Dissertation, xiii, 139 S. (2021)

Moeinzadeh, M.: De novo and haplotype assembly of polyploid genomes. Dissertation, vii, 157 S. (2019)

Ramisch, A.: Enhancer Prediction Based on Epigenomic Data. Dissertation, iv, 186 S. (2019)

Huska, M. R.: Using machine learning to predict and better understand DNA methylation and genomic enhancers. Dissertation, viii, 143 S., Freie Universität, Berlin (2018)

Helmuth, J.: Robust Normalization of Next Generation Sequencing Data. Dissertation, xii, 145 S. (2017)