Evidence map›Paper›PMID 41712760›Full record

ArticleBioinformatics (Oxford, England)2026

Accelerating minimap2 for whole-genome alignment.

Ghanshyam Chandra, Md Vasimuddin, Sanchit Misra, Chirag Jain

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ghanshyam ChandraDepartment of Computational and Data Sciences, Indian Institute of Science, Bangalore, KA 560012, India.ORCID 0000-0001-7687-4132
Md VasimuddinParallel Computing Lab, Intel Corporation, Bangalore, KA 560103, India.ORCID 0000-0001-7615-0388
Sanchit MisraParallel Computing Lab, Intel Corporation, Bangalore, KA 560103, India.
Chirag JainDepartment of Computational and Data Sciences, Indian Institute of Science, Bangalore, KA 560012, India.ORCID 0000-0002-4300-0794

Funding

DBT/Wellcome Trust India Alliance Fellowship IA/I/23/2/506979Intel India Research
6 · The paper itself

Abstract

summaryRecent advances in long-read sequencing and genome assembly techniques have enabled the generation of high-quality assemblies, often comprising megabase-scale sequences that span entire chromosomes. This results in longer but fewer sequences per genome, which affects the parallelization efficiency of whole-genome alignment tools. Current methods that assign one thread per query sequence now face suboptimal CPU use and longer runtimes because the processing of fewer sequences leaves many threads idle. We present mm2-plus, a fast and efficient method for whole-genome alignment, built upon the commonly used minimap2 aligner. Our improvements include a fine-grained parallel chaining algorithm and a fast method for differentiating primary and secondary chains. These optimizations accelerate the alignment of human, plant, and primate genomes by 1.6× to 7.2× without compromising accuracy. AVAILABILITY AND IMPLEMENTATION: Source code is available at https://github.com/at-cg/mm2-plus and https://doi.org/10.5281/zenodo.18220923.

Indexed as

GenomeGenomicsSequence AlignmentSoftwareAlgorithmsAnimalsHumansParallel AlgorithmsSequence Analysis, DNA

Identifiers

PMID41712760
PMCPMC12980334

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.