
AHMED DEBIT, PHD
GENOMICS, BIOINFORMATICS & COMPUTATIONAL BIOLOGY
Experienced computational biologist and bioinformatician with a strong scientific and technical background, including 7 years of expertise in genomics/transcriptomics, data analysis, statistics, and machine learning.
I currently work as a Postdoc - Bioinformatics at
Previously, I was a Research Fellow at the
I hold a PhD in Bioinformatics (cancer genomics), a master's degree in Bioinformatics and Modeling from the
I have authored 7+ publications in peer-reviewed scientific journals, released two software tools, and implemented/deployed an
See Google Scholar for a full publication list, including group authorships and pre-prints.
Selected Peer-reviewed journal articles & pre-prints
First author publications are underlined
Assessing Random Forest self-reproducibility for optimal short biomarker signature discovery. Briefings in Bioinformatics 2025
Evolutionary genomics of the emergence of brown algae as key components of coastal ecosystems. Cell 2024
LncPlankton V1.0: a comprehensive collection of plankton long non-coding RNAs. bioRxiv 2023
Differential expression patterns of long noncoding RNAs in a pleiomorphic diatom and relation to hyposalinity. Scientific Reports 2023
Differences in plasma microRNA content impair microRNA-based signature for breast cancer diagnosis in cohorts recruited from heterogeneous environmental sites.Scientific Reports 2021
Prevalence of histological characteristics of breast cancer in Rwanda in relation to age and tumor stages.Hormones and Cancer 2020
Software and tools
votingLNC: LncRNA identification through majority voting ensemble learning. Figshare 2023
stabFS: a stable feature selection based on random forest and stability measures Figshare 2023
Talks
Towards an Accurate Cancer Diagnosis Modelization: Comparison of Random Forest Strategies.
International Genetic Epidemiology Society IGES, 28th Annual Meeting, Houston TX, 2019
Biomarker Signatures Discovery to Support Cancer Diagnosis: Towards an Accurate and Robust Machine Learning Strategy.
SAB Medical-Genomics, Liege, Belgium, 2019
Algorithm Optimization for Diagnostic/Prognostic Signature Discovery in the Context of Breast Cancer.
GIGA Cancer, Liege, Belgium, 2018
Towards an Accurate Cancer Diagnosis Modelization: Comparison of Random Forest Strategies.
ByteMal, Liege, Belgium, 2018
Posters
SCANS: Assessing lncRNA conservation across species
JOBIM, 8-11 July 2025, Bordeaux
LncPlankton V1.0: a comprehensive collection of plankton long non-coding RNAs.
exRNA Research and Innovation to Improve Human and Plant Health, 11–13 June 2025, Hamburg
LncPlankton V1.0: a comprehensive collection of plankton long non-coding RNAs.
8th European Phycological Congress, 20-26 August 2023, Brest
Cellular and molecular characterization of short- and long-term hyposaline acclimation in a marine diatom: insights into the noncoding realm.
8th European Phycological Congress, 20-26 August 2023, Brest
Towards an Accurate Cancer Diagnosis Modelization: Comparison of Random Forest Strategies.
19th BeSHG meeting Precision Medicine: Application of Genetics in Prevention and Treatment, Liege, March 2019
Towards an Accurate Cancer Diagnosis Modelization: Comparison of Random Forest Strategies.
Joint meeting GIGA-Cancer Day 2018/EDT Cancerology, Liege, September 2018
Normalization and correction for batch effects via RUV for RNA-seq data: practical implications for Breast Cancer.
European Society of Human Genetics (ESHG 2017), Copenhagen, May 2017
Workshops
Applying the System Medicine Approach with Bioinformatics Tools in Research (OpenMultiMed), COST Action CA15120, TranslaTUM
Munich Germany, 18-20 March 2020
Elixir-IIB Carpentry Software
University of Milano Bicocca, February 22-23, 2018
Open Multiscale Systems Medicine (OpenMultiMed): Computational Tools for Systems Medicine, COST Action CA15120
MC Meeting Porto, Portugal, 20-23 February 2017
Multi-Omic Integrative Analysis of Gene Expression (MIAGE)
CIPF Valencia (Spain), 23-27 January 2017
WG2 COST Training Workshop on Interactions in Complex Disease Analysis
Antwerp, 27-28-29 April 2016
NGS Data Analysis: Variant calling and RNA-Seq
4 Days Workshop VIB Leuven (08/01, 15/01, 22/02, 26/02) 2016