Dr. Alexander Kel CEO And CSO

Prof. Dr. Alexander Kel

CEO & CSO, geneXplain GmbH, Wolfenbüttel, Germany  
Visiting Professor, Royal College of Surgeons in Ireland (RCSI), Dublin

Email:
alexander.kel(at)genexplain(dot)com

ORCID:
https://orcid.org/0000-0001-6775-2467

ResearchGate:
https://www.researchgate.net/profile/Alexander-Kel

Alexander Kel is a visionary in regulatory genomics and co-author of TRANSFAC and Genome Enhancer, driven by the mission to uncover life’s regulatory code and accelerate precision medicine, with nature walking and playing guitar as his grounding passions.

35+

years in bioinformatics

140+

scientific publications

20+

Leader of international research projects

Co-author of TRANSFAC® & Genome Enhancer

Profile

Prof. Dr. Alexander Kel is the CEO and CSO of geneXplain GmbH, a leading bioinformatics and systems medicine company based in Germany. He also serves as a Visiting Professor at the Royal College of Surgeons in Ireland (RCSI). He received his Ph.D. in Bioinformatics, Molecular Biology, and Genetics in 1990 after studying biology and mathematics at Novosibirsk State University, where he completed an M.S. in 1985 with a specialization in mathematical biology.

With more than 35 years of experience, Prof. Kel has contributed to nearly all major areas of modern bioinformatics: sequence analysis, gene recognition, promoter and enhancer prediction, RNA structure modeling, pathway reconstruction, systems biology, and drug-target discovery. He is a co-author of the TRANSFAC® database and the multi-omics, AI-powered analysis tool Genome Enhancer.

Prof. Kel introduced the “fuzzy puzzle” concept for modeling combinatorial gene regulation and developed the “walking pathways” algorithm for identifying master regulators in signaling and gene regulatory networks. His methods have been applied in over 20 national and international research projects focused on cancer, IBD, COPD, Parkinson’s disease, and other complex disorders. He has authored more than 140 scientific publications and multiple book chapters in bioinformatics and systems biology.

Scientific Expertise

  • RNA secondary structure prediction for long mRNAs
  • Analysis of short repeats and palindromes in coding sequences
  • Modeling translation mechanisms
  • Evolutionary simulations of prokaryotic genomes
  • Prediction of deletion/duplication hotspots in prokaryotes
  • Development of algorithms for functional site recognition in DNA
  • Recognition of splice sites and vertebrate promoters
  • Design of oligonucleotides for functional genomic regions
  • Genetic algorithm–based design of oligonucleotides for GPCRs
  • Development of regulatory databases (TRRD, TRANSFAC®, COMPEL)
  • Structural analysis of transcription-factor binding sites
  • Analysis of regulatory regions of immune- and cell-cycle-related genes
  • Reconstruction of cell-cycle regulatory networks
  • Genetic-algorithm methods for microarray data interpretation
  • Development of the BioUML systems biology platform and its commercial successor, the geneXplain® platform
  • Building global collaborative networks in computational biology

Selected International Grants

EU HORIZON-MISS-2023-CANCER-01 (2023–2027) – HIT-GLIO

Targeting tumor-host interactions in pediatric malignant gliomas to reinvigorate immunity and improve radio- and immunotherapy efficacy.

Eureka / BMBF (2022–2024)OxidoResist

Identification and validation of combinational therapies to overcome resistance to oxidative-stress-inducing anticancer drugs.

EU Horizon 2020 (2018–2022)COLOSSUS

Precision medicine and systems-based stratification in metastatic colorectal cancer.

ERA-PerMed (2018–2022)FindingMS:

Integrated prediction of early disease activity in multiple sclerosis.

Selected Publications

1. Myer P.A., Kim H., Blümel A.M., Finnegan E., Kel A., et al. (2022). Master transcription regulators… Gastro Hep Adv. 1: 328–341.

2. Orekhov A.N., Sukhorukov V.N., Nikiforov N.G., Kel A., et al. (2020). Signaling pathways potentially responsible for foam cell formation… Int. J. Mol. Sci. 21: 2716.

3. Kel A., Boyarskikh U., Stegmaier P., et al. (2019). Walking pathways with positive feedback loops reveal DNA methylation biomarkers of colorectal cancer. BMC Bioinformatics 20 (Suppl 4): 119.

4. Kolpakov F., Akberdin I., Yevshin I., Kel A., et al. (2019). BioUML: an integrated environment for systems biology… NAR 47(W1): W225–W233.

5. Kolmykov S., Yevshin I., Kel A., et al. (2020). GTRD: an integrated view of transcription regulation. NAR 49: D104–D111.

6. Lloyd K., Papoutsopoulou S., Stegmaier P., Kel A., et al. (2020). Systems medicine identifies a repurposable therapeutic agent for IBD. Dis. Model. Mech. 13: dmm044040.

7. Stegmaier P., Voss N., Meier T., Kel A., et al. (2011). Molecular switches for malignancy in an EGF mouse model of liver cancer. PLoS One 6(3): e17738.

8. Shi Y., Nikulenkov F., Zawacka-Pankau J., Kel A., et al. (2014). ROS-dependent activation of JNK converts p53 into an efficient oncogene inhibitor. Cell Death Differ. 21: 612–623.

9. Kel-Margoulis O.V., Romashchenko A.G., Kolchanov N.A., Wingender E., Kel A.E. (2000). COMPEL: a database on composite regulatory elements… NAR 28(1): 311–315.

10. Matys V., Kel-Margoulis O.V., Fricke E., Kel A.E., Wingender E. (2006). TRANSFAC and TRANSCompel. NAR 34: D108–D110.