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Gertjan Bisschop

dblp:346/8236 · DBLP profile ↗
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2ranked-venue papers
1as first author
2since 2021 · last 2024
0000-0001-8327-0142ORCID · corroborated

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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › population genetics › coalescent theory
ancestral recombination graph
0.812024
<tt>tstrait</tt> : a quantitative trait simulator for ancestral recombination graphs · Bioinform. 2024
Bioinformatics and computational biology
population genetics
0.812024
<tt>tstrait</tt> : a quantitative trait simulator for ancestral recombination graphs · Bioinform. 2024
Bioinformatics and computational biology › statistical genetics › genetic data simulation
quantitative trait simulation
0.812024
<tt>tstrait</tt> : a quantitative trait simulator for ancestral recombination graphs · Bioinform. 2024

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

ancestral recombination graph simulation · 0.8
YearPublicationVenuePosition
2024 <tt>tstrait</tt> : a quantitative trait simulator for ancestral recombination graphs
abstract
SUMMARY: Ancestral recombination graphs (ARGs) encode the ensemble of correlated genealogical trees arising from recombination in a compact and efficient structure and are of fundamental importance in population and statistical genetics. Recent breakthroughs have made it possible to simulate and infer ARGs at biobank scale, and there is now intense interest in using ARG-based methods across a broad range of applications, particularly in genome-wide association studies (GWAS). Sophisticated methods exist to simulate ARGs using population genetics models, but there is currently no software to simulate quantitative traits directly from these ARGs. To apply existing quantitative trait simulators users must export genotype data, losing important information about ancestral processes and producing prohibitively large files when applied to the biobank-scale datasets currently of interest in GWAS. We present tstrait, an open-source Python library to simulate quantitative traits on ARGs, and show how this user-friendly software can quickly simulate phenotypes for biobank-scale datasets on a laptop computer. AVAILABILITY AND IMPLEMENTATION: tstrait is available for download on the Python Package Index. Full documentation with examples and workflow templates is available on https://tskit.dev/tstrait/docs/, and the development version is maintained on GitHub (https://github.com/tskit-dev/tstrait).
Daiki Tagami, Gertjan Bisschop, Jerome Kelleher
Bioinform.2
2022 Graph-based algorithms for Laplace transformed coalescence time distributions
abstract
Extracting information on the selective and demographic past of populations that is contained in samples of genome sequences requires a description of the distribution of the underlying genealogies. Using the Laplace transform, this distribution can be generated with a simple recursive procedure, regardless of model complexity. Assuming an infinite-sites mutation model, the probability of observing specific configurations of linked variants within small haplotype blocks can be recovered from the Laplace transform of the joint distribution of branch lengths. However, the repeated differentiation required to compute these probabilities has proven to be a serious computational bottleneck in earlier implementations. Here, I show that the state space diagram can be turned into a computational graph, allowing efficient evaluation of the Laplace transform by means of a graph traversal algorithm. This general algorithm can, for example, be applied to tabulate the likelihoods of mutational configurations in non-recombining blocks. This work provides a crucial speed up for existing composite likelihood approaches that rely on the joint distribution of branch lengths to fit isolation with migration models and estimate the parameters of selective sweeps. The associated software is available as an open-source Python library, agemo.
Gertjan Bisschop
PLoS Comput. Biol.1