Evidence map›Paper›PMID 41654596›Full record

ArticleScientific data2026

Minimum virtual dataset for reproducible triploid de novo genome assembly.

Ryo Ootsuki

Abstract readDataset
In one paragraph

Article in Scientific data, 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

1 author.

Ryo OotsukiDepartment of Natural Sciences, Faculty of Arts and Sciences, Komazawa University, 1-23-1 Komazawa, Setagaya-ku, Tokyo, 154-8525, Japan. ootsuki@komazawa-u.ac.jp.ORCID http://orcid.org/0000-0003-2186-568X

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 26650146
6 · The paper itself

Abstract

Benchmark datasets for assessing polyploid genome assembly are limited because real polyploid genomes often contain unknown structural variations, complex repeats, and heterogeneous divergence among homologous copies. In this study, a minimal, fully controlled virtual dataset is provided for reproducible benchmarking of triploid de novo assembly using short reads. A 1-Mbp haploid reference sequence is generated and iteratively mutated to produce three genome copies (A-C) across 100 mutation steps, creating a divergence gradient that transitions from nearly identical to moderately diverged triploid genomes. For each divergence level, paired-end Illumina reads are simulated at uniform coverage and processed through error correction followed by de Bruijn graph assembly across multiple k-mer sizes. The dataset provides the full set of reference genomes, read sets, assemblies, and evaluation metrics, allowing direct reproduction of trends such as overcollapsed contigs at low divergence and improved genome separability at higher divergence. This compact resource offers method developers and users a transparent, reproducible standard for evaluating k-mer strategies and assembly behavior in triploid genomes.

Indexed as

TriploidySequence Analysis, DNA

Identifiers

PMID41654596
PMCPMC12992840

What OpenQuestion holds

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LicenceCC BY-NC-ND
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 OpenQuestion graph.