Evidence map›Paper›PMID 31231761›Full record

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

Highly multiplexed AmpliSeq technology identifies novel variation of flowering time-related genes in soybean (Glycine max).

Eri Ogiso-Tanaka, Takehiko Shimizu, Makita Hajika, Akito Kaga, Masao Ishimoto

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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. A single-nucleotide insertion in Rxp confers durable resistance to bacterial pustule in soybean.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Construction of prediction models for growth traits of soybean cultivars based on phenotyping in diverse genotype and environment combinations.DNA research : an international journal for rapid publication of reports on genes and genomes · 2022
    Article
  12. Article
  13. Validation of AmpliSeq NGS Panel forLife (Basel, Switzerland) · 2022
    Article
  14. Article
  15. Rapid excavating aMolecular breeding : new strategies in plant improvement · 2021
    Article
  16. Article
  17. Whole-genome sequence diversity and association analysis of 198 soybean accessions in mini-core collections.DNA research : an international journal for rapid publication of reports on genes and genomes · 2021
    Article
  18. Article
  19. Impacts of genomic research on soybean improvement in East Asia.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2020
    Review
  20. Article
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

5 authors.

Eri Ogiso-TanakaInstitute of Crop Science (NICS), NARO (National Agriculture and Food Research Organization), 2-1-2 Kannondai, Tsukuba, Ibaraki, Japan.
Takehiko ShimizuInstitute of Crop Science (NICS), NARO (National Agriculture and Food Research Organization), 2-1-2 Kannondai, Tsukuba, Ibaraki, Japan.
Makita HajikaInstitute of Crop Science (NICS), NARO (National Agriculture and Food Research Organization), 2-1-2 Kannondai, Tsukuba, Ibaraki, Japan.
Akito KagaInstitute of Crop Science (NICS), NARO (National Agriculture and Food Research Organization), 2-1-2 Kannondai, Tsukuba, Ibaraki, Japan.
Masao IshimotoInstitute of Crop Science (NICS), NARO (National Agriculture and Food Research Organization), 2-1-2 Kannondai, Tsukuba, Ibaraki, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole-genome re-sequencing is a powerful approach to detect gene variants, but it is expensive to analyse only the target genes. To circumvent this problem, we attempted to detect novel variants of flowering time-related genes and their homologues in soybean mini-core collection by target re-sequencing using AmpliSeq technology. The average depth of 382 amplicons targeting 29 genes was 1,237 with 99.85% of the sequence data mapped to the reference genome. Totally, 461 variants were detected, of which 150 sites were novel and not registered in dbSNP. Known and novel variants were detected in the classical maturity loci-E1, E2, E3, and E4. Additionally, large indel alleles, E1-nl and E3-tr, were successfully identified. Novel loss-of-function and missense variants were found in FT2a, MADS-box, WDR61, phytochromes, and two-component response regulators. The multiple regression analysis showed that four genes-E2, E3, Dt1, and two-component response regulator-can explain 51.1-52.3% of the variation in flowering time of the mini-core collection. Among them, the two-component response regulator with a premature stop codon is a novel gene that has not been reported as a soybean flowering time-related gene. These data suggest that the AmpliSeq technology is a powerful tool to identify novel alleles.

Indexed as

Genes, PlantPolymorphism, Single NucleotideTimeFlowersGenetic Association StudiesGlycine maxSequence Analysis, DNAAmpliSeqflowering time-related genegenotypingsoybeantarget re-sequencing

Identifiers

PMID31231761
PMCPMC6589554

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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.