Evidence map›Paper›PMID 30689773›Full record

ArticleDNA research : an international journal for rapid publication of reports on genes and genomes2019

De novo whole-genome assembly in Chrysanthemum seticuspe, a model species of Chrysanthemums, and its application to genetic and gene discovery analysis.

Hideki Hirakawa, Katsuhiko Sumitomo, Tamotsu Hisamatsu, Soichiro Nagano, Kenta Shirasawa, Yohei Higuchi, Makoto Kusaba, Masaji Koshioka, Yoshihiro Nakano, Masafumi Yagi and 4 more

Abstract read
In one paragraph

Article in DNA research : an international journal for rapid publication of reports on genes and genomes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

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  3. Chromosome-level genome assembly of the Gerbera (Gerbera hybrida) using HiFi long-read and Hi-C technologies.DNA research : an international journal for rapid publication of reports on genes and genomes · 2026
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  6. Assessing Functional Conservation AmongstPlants (Basel, Switzerland) · 2025
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  15. Review
  16. Creating novel ornamentalsFrontiers in plant science · 2023
    Review
  17. Review
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  19. Review
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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

14 authors.

Hideki HirakawaKazusa DNA Research Institute, Kisarazu, Chiba, Japan.
Katsuhiko SumitomoInstitute of Vegetable and Floriculture Sciences, NARO, Tsukuba, Ibaraki, Japan.
Tamotsu HisamatsuInstitute of Vegetable and Floriculture Sciences, NARO, Tsukuba, Ibaraki, Japan.
Soichiro NaganoKazusa DNA Research Institute, Kisarazu, Chiba, Japan.
Kenta ShirasawaKazusa DNA Research Institute, Kisarazu, Chiba, Japan.
Yohei HiguchiGraduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Makoto KusabaGraduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.
Masaji KoshiokaCollege of Bioresource Sciences, Nihon University, Kameino, Fujisawa, Kanagawa, Japan.
Yoshihiro NakanoInstitute of Vegetable and Floriculture Sciences, NARO, Tsukuba, Ibaraki, Japan.
Masafumi YagiInstitute of Vegetable and Floriculture Sciences, NARO, Tsukuba, Ibaraki, Japan.
Hiroyasu YamaguchiInstitute of Vegetable and Floriculture Sciences, NARO, Tsukuba, Ibaraki, Japan.
Kenji TaniguchiGraduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.
Michiharu NakanoGraduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.
Sachiko N IsobeKazusa DNA Research Institute, Kisarazu, Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cultivated chrysanthemum (Chrysanthemum morifolium Ramat.) is one of the most economically important ornamental crops grown worldwide. It has a complex hexaploid genome (2n = 6x = 54) and large genome size. The diploid Chrysanthemum seticuspe is often used as a model of cultivated chrysanthemum, since the two species are closely related. To expand our knowledge of the cultivated chrysanthemum, we here performed de novo whole-genome assembly in C. seticuspe using the Illumina sequencing platform. XMRS10, a C. seticuspe accession developed by five generations of self-crossing from a self-compatible strain, AEV2, was used for genome sequencing. The 2.72 Gb of assembled sequences (CSE_r1.0), consisting of 354,212 scaffolds, covered 89.0% of the 3.06 Gb C. seticuspe genome estimated by k-mer analysis. The N50 length of scaffolds was 44,741 bp. For protein-encoding genes, 71,057 annotated genes were deduced (CSE_r1.1_cds). Next, based on the assembled genome sequences, we performed linkage map construction, gene discovery and comparative analyses for C. seticuspe and cultivated chrysanthemum. The generated C. seticuspe linkage map revealed skewed regions in segregation on the AEV2 genome. In gene discovery analysis, candidate flowering-related genes were newly found in CSE_r1.1_cds. Moreover, single nucleotide polymorphism identification and annotation on the C. × morifolium genome showed that the C. seticuspe genome was applicable to genetic analysis in cultivated chrysanthemums. The genome sequences assembled herein are expected to contribute to future chrysanthemum studies. In addition, our approach demonstrated the usefulness of short-read genome assembly and the importance of choosing an appropriate next genome sequencing technology based on the purpose of the post-genome analysis.

Indexed as

Genetic LinkageGenome, PlantPolymorphism, GeneticWhole Genome SequencingChromosome MappingChrysanthemumMolecular Sequence AnnotationPhylogenyChrysanthemum seticuspeflowering genesgenome sequence assemblylinkage map

Identifiers

PMID30689773
PMCPMC6589549

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Registered trials

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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.