Evidence map›Paper›PMID 36251695›Full record

ArticlePLoS genetics2022

Prioritized candidate causal haplotype blocks in plant genome-wide association studies.

Xing Wu, Wei Jiang, Christopher Fragoso, Jing Huang, Geyu Zhou, Hongyu Zhao, Stephen Dellaporta

Abstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 citing papers in PubMed.

  1. Local Haplotyping Analysis for Flowering Time in Soybean Using Crosshap.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  2. Article
  3. Haplotype analysis and molecular marker development for the cold tolerance gene OsCTS11 at the seedling stage of rice.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
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

7 authors.

Xing WuDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut, United States of America.
Wei JiangDepartment of Biostatistics, Yale School of Public Health, Yale University, New Haven, Connecticut, United States of America.ORCID 0000-0001-6120-5278
Christopher FragosoDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut, United States of America.ORCID 0000-0001-5330-2588
Jing HuangDepartment of Applied Biological Science, Zhejiang University, Hangzhou, Zhejiang, China.
Geyu ZhouProgram of Computational Biology and Bioinformatics, Yale University, New Haven, Connecticut, United States of America.
Hongyu ZhaoDepartment of Biostatistics, Yale School of Public Health, Yale University, New Haven, Connecticut, United States of America.ORCID 0000-0003-1195-9607
Stephen DellaportaDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut, United States of America.ORCID 0000-0001-7452-3291

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Genome wide association studies (GWAS) can play an essential role in understanding genetic basis of complex traits in plants and animals. Conventional SNP-based linear mixed models (LMM) that marginally test single nucleotide polymorphisms (SNPs) have successfully identified many loci with major and minor effects in many GWAS. In plant, the relatively small population size in GWAS and the high genetic diversity found in many plant species can impede mapping efforts on complex traits. Here we present a novel haplotype-based trait fine-mapping framework, HapFM, to supplement current GWAS methods. HapFM uses genotype data to partition the genome into haplotype blocks, identifies haplotype clusters within each block, and then performs genome-wide haplotype fine-mapping to prioritize the candidate causal haplotype blocks of trait. We benchmarked HapFM, GEMMA, BSLMM, GMMAT, and BLINK in both simulated and real plant GWAS datasets. HapFM consistently resulted in higher mapping power than the other GWAS methods in high polygenicity simulation setting. Moreover, it resulted in smaller mapping intervals, especially in regions of high LD, achieved by prioritizing small candidate causal blocks in the larger haplotype blocks. In the Arabidopsis flowering time (FT10) datasets, HapFM identified four novel loci compared to GEMMA's results, and the average mapping interval of HapFM was 9.6 times smaller than that of GEMMA. In conclusion, HapFM is tailored for plant GWAS to result in high mapping power on complex traits and improved on mapping resolution to facilitate crop improvement.

Indexed as

Genome-Wide Association StudyQuantitative Trait LociAnimalsChromosome MappingGenotypeHaplotypesLinkage DisequilibriumPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID36251695
PMCPMC9612827

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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.