Evidence map›Paper›PMID 30194092›Full record

ArticleG3 (Bethesda, Md.)2018

Bulked-Segregant Analysis Coupled to Whole Genome Sequencing (BSA-Seq) for Rapid Gene Cloning in Maize.

Harry Klein, Yuguo Xiao, Phillip A Conklin, Rajanikanth Govindarajulu, Jacob A Kelly, Michael J Scanlon, Clinton J Whipple, Madelaine Bartlett

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed.

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  11. Novel Allelic Mutations inInternational journal of molecular sciences · 2024
    Article
  12. Identification of Dwarfing Candidate Genes inPlants (Basel, Switzerland) · 2024
    Article
  13. Function Analysis of a Maize Endo-1,4-β-xylanase GeneInternational journal of molecular sciences · 2024
    Article
  14. Article
  15. Article
  16. Genetic characterization of a locus responsible for low pungency using EMS-induced mutants in Capsicum annuum L.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    Article
  17. Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  18. Article
  19. Article
  20. Versatile mapping-by-sequencing with Easymap v.2.Frontiers in plant science · 2023
    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

8 authors.

Harry KleinPlant Biology Graduate Program and Biology Department, University of Massachusetts Amherst, Amherst, MA 01003.
Yuguo XiaoDepartment of Biology, Brigham Young University, 4102 LSB, Provo, UT 84602.ORCID 0000-0002-0747-5856
Phillip A ConklinDepartment of Plant Biology, Cornell University, Ithaca, NY 14853.
Rajanikanth GovindarajuluDepartment of Biology, West Virginia University, Morgantown, WV 26506.
Jacob A KellyDepartment of Biology, Brigham Young University, 4102 LSB, Provo, UT 84602.
Michael J ScanlonDepartment of Plant Biology, Cornell University, Ithaca, NY 14853.
Clinton J WhippleDepartment of Biology, Brigham Young University, 4102 LSB, Provo, UT 84602.
Madelaine BartlettPlant Biology Graduate Program and Biology Department, University of Massachusetts Amherst, Amherst, MA 01003 mbartlett@bio.umass.edu.ORCID 0000-0002-0369-8606

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Forward genetics remains a powerful method for revealing the genes underpinning organismal form and function, and for revealing how these genes are tied together in gene networks. In maize, forward genetics has been tremendously successful, but the size and complexity of the maize genome made identifying mutant genes an often arduous process with traditional methods. The next generation sequencing revolution has allowed for the gene cloning process to be significantly accelerated in many organisms, even when genomes are large and complex. Here, we describe a bulked-segregant analysis sequencing (BSA-Seq) protocol for cloning mutant genes in maize. Our simple strategy can be used to quickly identify a mapping interval and candidate single nucleotide polymorphisms (SNPs) from whole genome sequencing of pooled F2 individuals. We employed this strategy to identify

Indexed as

Genes, PlantHigh-Throughput Nucleotide SequencingCloning, MolecularMutationPolymorphism, Single NucleotideZea maysbulked-segregant analysisforward geneticsmaize geneticsmutant genesnext generation sequencing

Identifiers

PMID30194092
PMCPMC6222591

What OpenQuestion holds

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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 OpenQuestion graph.