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Palle Duun Rohde

dblp:191/7393 · DBLP profile ↗
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2ranked-venue papers
2as first author
1since 2021 · last 2023
0000-0003-4347-8656ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author · 1 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 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › statistical genetics
genomic prediction
1.122023
Expanded utility of the R package, qgg, with applications within genomic medicine · Bioinform. 2023
qgg: an R package for large-scale quantitative genetic analyses · Bioinform. 2020
Bioinformatics and computational biology › statistical genetics
quantitative genetics
1.122023
Expanded utility of the R package, qgg, with applications within genomic medicine · Bioinform. 2023
qgg: an R package for large-scale quantitative genetic analyses · Bioinform. 2020
Bioinformatics and computational biology › statistical genetics
heritability estimation
0.212023
Expanded utility of the R package, qgg, with applications within genomic medicine · Bioinform. 2023
Bioinformatics and computational biology › statistical genetics
association analysis
0.112020
qgg: an R package for large-scale quantitative genetic analyses · Bioinform. 2020

Methods — techniques the papers use, named apart from their topics

markov chain monte carlo · 0.7bayesian linear regression · 0.7mixed linear model · 0.4genomic relationship matrix · 0.4
YearPublicationVenuePosition
2023 Expanded utility of the R package, qgg, with applications within genomic medicine
abstract
SUMMARY: Here, we present an expanded utility of the R package qgg for genetic analyses of complex traits and diseases. One of the major updates of the package is, that it now includes Bayesian linear regression modeling procedures, which provide a unified framework for mapping of genetic variants, estimation of heritability and genomic prediction from either individual level data or from genome-wide association study summary data. With this release, the qgg package now provides a wealth of the commonly used methods in analysis of complex traits and diseases, without the need to switch between software and data formats. AVAILABILITY AND IMPLEMENTATION: The methodologies are implemented in the publicly available R software package, qgg, using fast and memory efficient algorithms in C++ and is available on CRAN or as a developer version at our GitHub page (https://github.com/psoerensen/qgg). Notes on the implemented statistical genetic models, tutorials and example scripts are available at our GitHub page https://psoerensen.github.io/qgg/.
Palle Duun Rohde, Izel Fourie Sørensen, Peter Sørensen
Bioinform.1
2020 qgg: an R package for large-scale quantitative genetic analyses
abstract
SUMMARY: Here, we present the R package qgg, which provides an environment for large-scale genetic analyses of quantitative traits and diseases. The qgg package provides an infrastructure for efficient processing of large-scale genetic data and functions for estimating genetic parameters, and performing single and multiple marker association analyses and genomic-based predictions of phenotypes. AVAILABILITY AND IMPLEMENTATION: The qgg package is freely available. For the latest updates, user guides and example scripts, consult the main page http://psoerensen.github.io/qgg. The current release is available from CRAN (https://CRAN.R-project.org/package=qgg) for all major operating systems. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Palle Duun Rohde, Izel Fourie Sørensen, Peter Sørensen
Bioinform.1