Highly repetitive sequences pose problems for genome assembly and analysis. While advances in long-read sequencing technologies have helped reveal the organization of repetitive genomic sequences at unprecedented resolution, their functional characterization remains difficult because molecular assays that probe protein-DNA interactions and characterize expression often rely on short read sequencing. The repetitive nature of these regions poses major challenges for methods relying on sequence mapping, which is exacerbated for short reads. Repetitive genome regions often have low mappability, leading to substantial information loss during downstream filtering. To address this challenge, we developed a bioinformatic tool -kmerRRR- that leverages k-mer frequency analyses to enhance the mappability of repetitive regions. KmerRRR compares k-mer frequencies within user-defined loci to their frequencies across the genome to identify repetitive sequences that are overrepresented locally relative to the global background. This approach quantifies locus uniqueness, allowing users to distinguish sequences that are globally repetitive from those that are repetitive, but restricted to specific genomic loci. We demonstrated the utility of this method by reanalyzing chromatin profiling data from human, Drosophila, and Arabidopsis centromeres and small RNA sequencing data. Our results show that incorporating local k-mer ratio information enhances read retention and signal interpretation within repetitive regions, thereby recovering biologically meaningful information that is typically lost in conventional analyses. The tool is freely available under MIT license in github: (https://github.com/LarracuenteLab/kmerRRR).
Rahmat, J., Pham, T. M., Larracuente, A. M.
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