Veerle Fack

Dr. Veerle Fack

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 May 2018 in BMC Bioinformatics
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HBHerman De Beukelaer
Herman De Beukelaer
GDGuy F Davenport
Guy F Davenport
VFVeerle Fack
Veerle Fack
Core collections provide genebank curators and plant breeders a way to reduce size of their collections and populations, while minimizing impact on genetic diversity and allele frequency. Many methods have been proposed to generate core collections, often using distance metrics to quantify the similarity of two accessions, based on genetic marker data or phenotypic traits. Core Hunter is a multi-purpose core subset selection tool that uses local search algorithms to generate subsets relying on one or more metrics, including several distance metrics and allelic richness. In version 3 of Core Hunter (CH3) we have incorporated two new, improved methods for summarizing distances to quantify diversity or representativeness of the core collection. A comparison of CH3 and Core Hunter 2 (CH2) showed that these new metrics can be effectively optimized with less complex algorithms, as compared to those used in CH2. CH3 is more effective at maximizing the improved diversity metric than CH2, still ensures a high average and minimum distance, and is faster for large datasets. Using CH3, a simple stochastic hill-climber is able to find highly diverse core collections, and the more advanced parallel tempering algorithm further increases the quality of the core and further reduces variability across independent samples. We also evaluate the ability of CH3 to simultaneously maximize diversity, and either representativeness or allelic richness, and compare the results with those of the GDOpt and SimEli methods. CH3 can sample equally representative cores as GDOpt, which was specifically designed for this purpose, and is able to construct cores that are simultaneously more diverse, and either are more representative or have higher allelic richness, than those obtained by SimEli. In version 3, Core Hunter has been updated to include two new core subset selection metrics that construct cores for representativeness or diversity, with improved performance. It combines and outperforms the strengths of other methods, as it (simultaneously) optimizes a variety of metrics. In addition, CH3 is an improvement over CH2, with the option to use genetic marker data or phenotypic traits, or both, and improved speed. Core Hunter 3 is freely available on http://www.corehunter.org .

23 November 2012 in BMC Bioinformatics
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HBHerman De Beukelaer
Herman De Beukelaer
Petr SmykalPetr Smykal
Petr Smykal
GDGuy F Davenport
Guy F Davenport
VFVeerle Fack
Veerle Fack
Sampling core subsets from genetic resources while maintaining as much as possible the genetic diversity of the original collection is an important but computationally complex task for gene bank managers. The Core Hunter computer program was developed as a tool to generate such subsets based on multiple genetic measures, including both distance measures and allelic diversity indices. At first we investigate the effect of minimum (instead of the default mean) distance measures on the performance of Core Hunter. Secondly, we try to gain more insight into the performance of the original Core Hunter search algorithm through comparison with several other heuristics working with several realistic datasets of varying size and allelic composition. Finally, we propose a new algorithm (Mixed Replica search) for Core Hunter II with the aim of improving the diversity of the constructed core sets and their corresponding generation times.

1 June 2017 in Genetics
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Journal Article
Closed access
HBHerman De Beukelaer
Herman De Beukelaer
YBYvonne Badke
Yvonne Badke
VFVeerle Fack
Veerle Fack
GMGeert De Meyer
Geert De Meyer
Long-term genomic selection (GS) requires strategies that balance genetic gain with population diversity, to sustain progress for traits under selection, and to keep diversity for future breeding. In a simulation model for a recurrent selection scheme, we provide the first head-to-head comparison of two such existing strategies: genomic optimal contributions selection (GOCS), which limits realized genomic relationship among selection candidates, and weighted genomic selection (WGS), which upscales rare allele effects in GS. Compared to GS, both methods provide the same higher long-term genetic gain and a similar lower inbreeding rate, despite some inherent limitations. GOCS does not control the inbreeding rate component linked to trait selection, and, therefore, does not strike the optimal balance between genetic gain and inbreeding. This makes it less effective throughout the breeding scheme, and particularly so at the beginning, where genetic gain and diversity may not be competing. For WGS, truncation selection proved suboptimal to manage rare allele frequencies among the selection candidates. To overcome these limitations, we introduce two new set selection methods that maximize a weighted index balancing genetic gain with controlling expected heterozygosity (IND-HE) or maintaining rare alleles (IND-RA), and show that these outperform GOCS and WGS in a nearly identical way. While requiring further testing, we believe that the inherent benefits of the IND-HE and IND-RA methods will transfer from our simulation framework to many practical breeding settings, and are therefore a major step forward toward efficient long-term genomic selection.

24 January 2013 in Bioinformatics
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Journal Article
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MVMichaël Vyverman
Michaël Vyverman
Bernard De BaetsBernard De Baets
Bernard De Baets
VFVeerle Fack
Veerle Fack
PDPeter Dawyndt
Peter Dawyndt
Summary: We have developed essaMEM, a tool for finding maximal exact matches that can be used in genome comparison and read mapping. essaMEM enhances an existing sparse suffix array implementation with a sparse child array. Tests indicate that the enhanced algorithm for finding maximal exact matches is much faster, while maintaining the same memory footprint. In this way, sparse suffix arrays remain competitive with the more complex compressed suffix arrays. Availability: Source code is freely available at https://github.ugent.be/ComputationalBiology/essaMEM. Contact:Michael.Vyverman@UGent.be Supplementary information: Supplementary data are available at Bioinformatics online.

1 October 2006 in Designs, Codes and Cryptography
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Iliya BouyuklievIliya Bouyukliev
Iliya Bouyukliev
VFVeerle Fack
Veerle Fack
WWWolfgang Willems
Wolfgang Willems
JWJoost Winne
Joost Winne

13 October 2007 in Designs, Codes and Cryptography
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Journal Article
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VFVeerle Fack
Veerle Fack
SFSzabolcs L. Fancsali
Szabolcs L. Fancsali
LSL. Storme
L. Storme
GVGeetrui Van de Voorde
Geetrui Van de Voorde
JWJoost Winne
Joost Winne