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Renders, L.

Publications and source records attributed to Renders, L..

2 recordsLinked to original sources

Columba: Fast Approximate Pattern Matching withOptimized Search Schemes

Aligning sequencing reads to reference genomes is a fundamental task in bioinformatics. Aligners can be classified as lossy or lossless: lossy aligners prioritize speed by reporting only one or a few high-scoring alignments, whereas lossless aligners output all optimal alignments, ensuring completeness and sensitivity. This paper introduces Columba, a high-performance lossless aligner tailored for Illumina sequencing data. Columba processes single or paired-end reads in FASTQ format and outputs alignments in SAM format. By utilizing advanced search schemes and bit-parallel alignment techniques, Columba achieves exceptional speed. Columba is available in two variants. The first is based on the bidirectional FM-index. The second, Columba RLC, employs run-length compression using a bidirectional move structure, significantly reducing memory usage for large, repetitive datasets like pan-genomes. Through extensive benchmarking, Columba outperforms existing lossless aligners in speed, particularly at higher error rates. Tests on the human genome and bacterial and human pan-genome datasets demonstrate Columbas robustness and efficiency. We integrated Columba into the OptiType HLA genotyping pipeline, where it substantially reduced computational time while maintaining accuracy. These results position Columba as a versatile, state-of-the-art tool for high-sensitivity genomic analyses.

bioinformatics↗

b-move: faster bidirectional character extensions in a run-length compressed index

Due to the increasing availability of high-quality genome sequences, pan-genomes are gradually replacing single consensus reference genomes in many bioinformatics pipelines to better capture genetic diversity. Traditional bioinformatics tools using the FM-index face memory limitations with such large genome collections. Recent advancements in run-length compressed indices like Gagie et al.s r-index and Nishimoto and Tabeis move structure, alleviate memory constraints but focus primarily on backward search for MEM-finding. Arakawa et al.s br-index initiates complete approximate pattern matching using bidirectional search in run-length compressed space, but with significant computational overhead due to complex memory access patterns. We introduce b-move, a novel bidirectional extension of the move structure, enabling fast, cache-efficient bidirectional character extensions in run-length compressed space. It achieves bidirectional character extensions up to 8 times faster than the br-index, closing the performance gap with FM-index-based alternatives, while maintaining the br-indexs favorable memory characteristics. For example, all available complete E. coli genomes on NCBIs RefSeq collection can be compiled into a b-move index that fits into the RAM of a typical laptop. Thus, b-move proves practical and scalable for pan-genome indexing and querying. We provide a C++ implementation of b-move, supporting efficient lossless approximate pattern matching including locate functionality, available at https://github.com/biointec/b-move under the AGPL-3.0 license. FundingLore Depuydt: PhD Fellowship FR (1117322N), Research Foundation - Flanders (FWO) Luca Renders: PhD Fellowship SB (1SE7822N), Research Foundation - Flanders (FWO) Travis Gagie: NSERC Discovery Grant RGPIN-07185-2020 to Travis Gagie and NIH grant R01HG011392 to Ben Langmead

bioinformatics↗