ArticleGenome research2025
Fast sequence alignment for centromeres with RaMA.
Article in Genome research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Enabling efficient and robust analysis of tandem repeats in genomic data using Wavefront-based String Decomposer.Genome research · 2026Article
- mm2-ivh: simple and precise overlap detection in alpha satellite HORs with interval hashing.Bioinformatics (Oxford, England) · 2026Article
- HAlign-G: rapid and low-memory multiple-genome aligner for large-scale closely related genomes.Genome biology · 2025Article
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Authors and funding
5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
The release of the first draft of the human pangenome has revolutionized genomic research by enabling access to complex regions like centromeres, composed of extra-long tandem repeats (ETRs). However, a significant gap remains as current methodologies are inadequate for producing sequence alignments that effectively capture genetic events within ETRs, highlighting a pressing need for improved alignment tools. Inspired by UniAligner, we developed a rare match aligner (RaMA), using rare matches as anchors and two-piece affine gap cost to generate complete pairwise alignment that better captures genetic evolution. RaMA also employs parallel computing and the wavefront algorithm to accelerate anchor discovery and sequence alignment, achieving up to 13.66 times faster processing using only 11% of UniAligner's memory. Downstream analysis of simulated data and the CHM13 and CHM1 higher-order repeat (HOR) arrays demonstrates that RaMA achieves more accurate alignments, effectively capturing true HOR structures. RaMA also introduces two methods for defining reliable alignment regions, further refining and enhancing the accuracy of centromeric alignment statistics.
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