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MANUDB: database and application to retrieve and visualize mammalian NUMTs
Bálint Biró1,2, Zoltán Gál2, Zsófia Nagy2
1Group BM, Data Insights Team, _VOIS, Kerepesi str. 35, Budapest, 1087, Hungary.
Database : the Journal of Biological Databases and Curation
|February 22, 2025
Summary
Mitochondrial DNA sequences are transferring to the nuclear genome, impacting evolution and cancer. A new database, MANUDB, provides access to these integrated mammalian sequences for research.
Area of Science:
- Genetics
- Genomics
- Evolutionary Biology
Background:
- Mitochondrial DNA (mtDNA) sequences are increasingly found integrated into the nuclear genome.
- These integrated sequences play roles in evolutionary processes and disease, including cancer.
- They also pose challenges for accurate genome assembly and phylogenetic/forensic analyses.
Purpose of the Study:
- To introduce MANUDB, a publicly accessible database of mammalian nuclear mitochondrial sequences.
- To provide a centralized resource for studying the integration of mitochondrial DNA into the nuclear genome.
- To facilitate research on the evolutionary and functional implications of these genomic events.
Main Methods:
- Development of a computational pipeline for identifying nuclear-integrated mitochondrial sequences in mammalian genomes.
- Curating and organizing identified sequences into a comprehensive database.
- Implementing a user-friendly interface for data retrieval and visualization.
Main Results:
- MANUDB is established, offering a uniform dataset of integrated mitochondrial sequences across mammalian species.
- The database allows users to access and visualize specific mitochondrial genome fragments within nuclear genomes.
- This resource consolidates findings from a previously developed identification pipeline.
Conclusions:
- MANUDB serves as a valuable resource for the scientific community, enabling further investigation into mitochondrial-nuclear interactions.
- The database supports research in evolutionary biology, cancer genomics, and bioinformatics.
- Public accessibility of these integrated sequences promotes advancements in genome analysis and understanding.

