Evidence map›Paper›PMID 41618433›Full record

ArticleGenome biology2026

Benchmarking alignment strategies for Hi-C reads in metagenomic Hi-C data.

Yuqiu Wang, Wenxuan Zuo, Jiawei Huang, Fengzhu Sun, Yuxuan Du

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Article in Genome biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Yuqiu WangDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, 90089, CA, USA.
Wenxuan ZuoDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, 90089, CA, USA.
Jiawei HuangDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, 90089, CA, USA.
Fengzhu SunDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, 90089, CA, USA. fsun@usc.edu.
Yuxuan DuDepartment of Electrical Engineering, The University of Texas at San Antonio, San Antonio, 78249, TX, USA. yuxuan.du@utsa.edu.

Funding

National Science Foundation EF-2125142
6 · The paper itself

Abstract

backgroundMetagenomics combined with High-throughput Chromosome Conformation Capture (Hi-C) provides a powerful approach to study microbial communities by linking genomic content with spatial interactions. Hi-C complements shotgun sequencing by revealing taxonomic composition, functional interactions, and genomic organization within a single sample. However, aligning Hi-C reads to metagenomic contigs is challenging due to variable insert sizes of Hi-C paired-end reads, multi-species complexity, and gaps in assemblies. Although several benchmark studies have evaluated general alignment tools and Hi-C data alignment, none have specifically focused on metagenomic Hi-C data.

resultsWe evaluated seven alignment strategies commonly used in Hi-C analyses: BWA MEM -5SP, BWA MEM default, BWA aln default, Bowtie2 default, Bowtie2 -very-sensitive-local, Minimap2 default, and Chromap Hi-C default. We benchmarked these tools on one synthetic dataset and seven real-world environments. Performance was assessed based on the number of inter-contig Hi-C read pairs and their impact on downstream tasks, such as binning quality.

conclusionsWe show that BWA MEM -5SP generally outperformed all other tools across most environments in terms of inter-contig read pairs and binning quality, followed by BWA MEM default. Chromap and Minimap2, while less effective in these metrics, demonstrated the highest computational efficiency.

Indexed as

MetagenomicsSequence AlignmentAlgorithmsBenchmarkingHigh-Throughput Nucleotide SequencingSoftwareBenchmarkingHi-C MetagenomicsSequence Alignment

Identifiers

PMID41618433
PMCPMC12964890

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.