Demo Data from EDBT 2026 / reviewers in the wild / expert
Jacob I Marsh
dblp:370/6094
· DBLP profile ↗
2ranked-venue papers
1as first author
2since 2021 · last 2025
0000-0003-3734-2023ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 2 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
2 papers |
Bioinformatics and computational biology · 100% |
Topics — the 5 heaviest of 5, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics
genome-wide association study |
1.5 | 2 | 2025 | HaploVar: an R package for defining local haplotype variants for trait association and trait prediction analyses · Bioinform. 2025 crosshap: R package for local haplotype visualization for trait association analysis · Bioinform. 2023 |
Bioinformatics and computational biology › statistical genetics › genomic prediction
genomic selection |
0.9 | 1 | 2025 | HaploVar: an R package for defining local haplotype variants for trait association and trait prediction analyses · Bioinform. 2025 |
Bioinformatics and computational biology › statistical genetics › haplotype analysis
haplotype-based association testing |
0.9 | 1 | 2025 | HaploVar: an R package for defining local haplotype variants for trait association and trait prediction analyses · Bioinform. 2025 |
Bioinformatics and computational biology › statistical genetics
genetic linkage analysis |
0.7 | 1 | 2023 | crosshap: R package for local haplotype visualization for trait association analysis · Bioinform. 2023 |
Bioinformatics and computational biology
genomics |
0.7 | 1 | 2023 | crosshap: R package for local haplotype visualization for trait association analysis · Bioinform. 2023 |
Methods — techniques the papers use, named apart from their topics
haplotype analysis · 0.9density-based clustering · 0.7
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | HaploVar: an R package for defining local haplotype variants for trait association and trait prediction analysesabstractSUMMARY: Marker assisted breeding (MAB) supports breeding by identifying individuals or molecular markers associated with important traits. MAB methods include genome-wide association studies (GWAS) and genomic selection (GS). Local haplotypes are regions of DNA that are inherited together due to high levels of linkage disequilibrium. Local haplotypes can improve the prediction accuracy and power of GS and GWAS. Currently available local haplotyping tools improve GWAS power through fine-mapping of candidate regions or through haplotype-based GWAS. However, no local haplotyping tools utilize the benefits of haplotypes for GS. Here we present HaploVar, a local haplotyping tool designed to improve both GWAS and GS pipelines by identifying local haplotypes and formatting the output to be compatible with all major GWAS and GS tools. HaploVar can be used in any haplotype-based MAB study. AVAILABILITY AND IMPLEMENTATION: HaploVar can be downloaded from CRAN with R > 4.0.0 (DOI: 10.32614/CRAN.package.HaploVar). HaploVar and a tutorial vignette is available on GitHub (https://github.com/TessaMacNish/HaploVar). HaploVar is available under an MIT license. SUPPLEMENTARY INFORMATION: Supplementary material is available at Bioinformatics online. Tessa R. Macnish, Hawlader A. Al-Mamun, Thomas Bergmann, Mitchell S. Bestry, Jacob I Marsh, David Edwards |
Bioinform. | 5 |
| 2023 | crosshap: R package for local haplotype visualization for trait association analysisabstractSUMMARY: Genome-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/). Jacob I Marsh, Jakob Petereit, Brady A Johnston, Philipp E. Bayer, Cassandria G. Tay Fernandez, Hawlader A. Al-Mamun, Jacqueline Batley, David Edwards |
Bioinform. | 1 |