Yeast rDNA as a benchmark for rDNAmine repeat analysis pipeline
Abstract
In this study, we introduce a novel approach for analysing long, repetitive genomic sequences. Our methods significantly advance research on rDNA polymorphism. First, we describe a technique for isolating high-molecular-weight DNA from individual chromosomes, enabling selective enrichment of sequencing libraries for extensive genomic regions of interest. Second, we present rDNAmine, a bioinformatic toolkit for capturing and examining large repetitive arrays in Oxford Nanopore sequencing data. This approach facilitates the study of polymorphisms within long repeats, bypassing traditional alignment-based methods and providing a more efficient and scalable solution for investigating repetitive regions. We demonstrate the effectiveness of our approach through the analysis of rDNA arrays in two yeast species, Saccharomyces cerevisiae and Candida albicans. In S. cerevisiae, rDNA arrays show limited polymorphism, while in C. albicans, we observe substantial variation in rDNA module size, with two distinct repeat populations within the array. These findings reveal species-specific differences in the structural organisation of rDNA loci, highlighting the diverse nature of tandem repeat architecture. The rDNAmine toolkit is broadly applicable to various organisms and repetitive genomic contexts, offering a versatile platform for studying repetitive sequences. Take AwayO_LIYeast rDNA serves as a benchmark to validate tools for analysing long repetitive sequences. C_LIO_LIA chromosome-specific DNA extraction method has been introduced to enable targeted enrichment of repetitive loci. C_LIO_LIThe rDNAmine pipeline was designed to analyse long tandem repeats from noisy long-read data without requiring global alignment. C_LI
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 29th percentile
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Ribotin: Automated assembly and phasing of rDNA morphs
Mikko Rautiainen·BioinformaticsPeer-reviewed·Mar 1, 2024
- Quantification of disease-associated RNA tandem repeats by nanopore sensing
Gerardo Patiño‐Guillén, Jovan Pešović, … Filip Bošković·Nature CommunicationsPeer-reviewed·May 8, 2026
- rDNAcaller: a fast and robust pipeline to call ribosomal DNA variants
Jose Miguel Ramirez, Winona Oliveros, … Marta Melé·NAR Genomics and BioinformaticsPeer-reviewed·Oct 7, 2025
- A new method for determining ribosomal DNA copy number shows differences between Saccharomyces cerevisiae populations
Diksha Sharma, Sylvie Hermann‐Le Denmat, … Austen R. D. Ganley·GenomicsPeer-reviewed·Jul 1, 2022
- Genome-wide characterization of satellite DNA arrays in a complex plant genome using nanopore reads
Tihana Vondrak, Laura Ávila Robledillo, … Jir̆ı́ Macas·The Plant JournalPeer-reviewed·Sep 27, 2019
- Ultrafast, alignment-free detection of repeat expansions in next-generation DNA and RNA sequencing data
Liam G. Fearnley, Mark F. Bennett, Melanie Bahlo·bioRxiv·Apr 5, 2021