Evidence map›Paper›PMID 37607004›Full record

ReviewBioinformatics (Oxford, England)2023

crosshap: R package for local haplotype visualization for trait association analysis.

Jacob I Marsh, Jakob Petereit, Brady A Johnston, Philipp E Bayer, Cassandria G Tay Fernandez, Hawlader A Al-Mamun, Jacqueline Batley, David Edwards

Abstract readReview
In one paragraph

Review in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Integrating multi-omics and machine learning for disease resistance prediction in legumes.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
    Review
  8. Article
  9. 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.

Jacob I MarshCentre for Applied Bioinformatics, University of Western Australia, Perth WA, 6009, Australia.ORCID 0000-0003-3734-2023
Jakob PetereitCentre for Applied Bioinformatics, University of Western Australia, Perth WA, 6009, Australia.ORCID 0000-0003-2159-0380
Brady A JohnstonSchool of Molecular Sciences, University of Western Australia, Perth WA, 6009, Australia.ORCID 0000-0001-6301-2269
Philipp E BayerCentre for Applied Bioinformatics, University of Western Australia, Perth WA, 6009, Australia.ORCID 0000-0001-8530-3067
Cassandria G Tay FernandezCentre for Applied Bioinformatics, University of Western Australia, Perth WA, 6009, Australia.
Hawlader A Al-MamunCentre for Applied Bioinformatics, University of Western Australia, Perth WA, 6009, Australia.
Jacqueline BatleyCentre for Applied Bioinformatics, University of Western Australia, Perth WA, 6009, Australia.ORCID 0000-0002-5391-5824
David EdwardsCentre for Applied Bioinformatics, University of Western Australia, Perth WA, 6009, Australia.ORCID 0000-0001-7599-6760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summaryGenome-wide association studies (GWAS) excels at harnessing dense genomic variant datasets to identify candidate regions responsible for producing a given phenotype. However, GWAS and traditional fine-mapping methods do not provide insight into the complex local landscape of linkage that contains and has been shaped by the causal variant(s). Here, we present crosshap, an R package that performs robust density-based clustering of variants based on their linkage profiles to capture haplotype structures in a local genomic region of interest. Following this, crosshap is equipped with visualization tools for choosing optimal clustering parameters (ɛ) before producing an intuitive figure that provides an overview of the complex relationships between linked variants, haplotype combinations, phenotype, and metadata traits. AVAILABILITY AND IMPLEMENTATION: The crosshap package is freely available under the MIT license and can be downloaded directly from CRAN with R >4.0.0. The development version is available on GitHub alongside issue support (https://github.com/jacobimarsh/crosshap). Tutorial vignettes and documentation are available (https://jacobimarsh.github.io/crosshap/).

Indexed as

DocumentationGenome-Wide Association StudyCluster AnalysisHaplotypesPhenotype

Identifiers

PMID37607004
PMCPMC10471896

What OpenQuestion holds

Textmetadata
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.