Michaël Vyverman
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Michaël Vyverman has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Peter Dawyndt
Ghent University, Ghent, Belgium
4 shared publications - Bernard De Baets
KERMIT, Department of Data Analysis and Mathematical Modelling, Ghent University, Gent, Belgium
3 shared publications - Veerle Fack
Department of Applied Mathematics, Computer Science and Statistics, Ghent University, Ghent, Belgium
3 shared publications Joachim De Schrijver
1 shared publicationVeerle Fack
Department of Applied Mathematics and Computer Science, Ghent University, Building S9, 281 Krijgslaan and Department of Mathematical Modelling, Statistics and Bioinformatics, Ghent University, 653 Coupure links, Ghent, B-9000, Belgium
1 shared publicationWim Van Criekinge
1 shared publication
Latest Publications
- Open Access
- 15 May 2015
- Published by Springer Nature in BMC Bioinformatics
- Vol. 16 (1) , 1-11
A Long Fragment Aligner called ALFALFA
Rapid evolutions in sequencing technology force read mappers into flexible adaptation to longer reads, changing error models, memory barriers and novel applications. ALFALFA achieves a high performance in accurately mapping long single-end and paired-end reads to gigabase-scale reference genomes, while remaining competitive for mapping shorter reads. Its seed-and-extend workflow is underpinned by fast retrieval of super-maximal exact matches from an enhanced sparse suffix array, with flexible parameter tuning to balance performance, memory footprint and accuracy. ALFALFA is open source and available at http://alfalfa.ugent.be .
- 15 May 2015
- Published by Springer Nature in BMC Bioinformatics
- Vol. 16 (1) , 1-11
Open AccessA Long Fragment Aligner called ALFALFA
Rapid evolutions in sequencing technology force read mappers into flexible adaptation to longer reads, changing error models, memory barriers and novel applications. ALFALFA achieves a high performance in accurately mapping long single-end and paired-end reads to gigabase-scale reference genomes, while remaining competitive for mapping shorter reads. Its seed-and-extend workflow is underpinned by fast retrieval of super-maximal exact matches from an enhanced sparse suffix array, with flexible parameter tuning to balance performance, memory footprint and accuracy. ALFALFA is open source and available at http://alfalfa.ugent.be .
- Open Access
- 24 January 2013
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 29 (6) , 802-804
essaMEM: finding maximal exact matches using enhanced sparse suffix arrays
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.
- 24 January 2013
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 29 (6) , 802-804
Open AccessessaMEM: finding maximal exact matches using enhanced sparse suffix arrays
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.
- Open Access
- 12 May 2012
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 40 (15) , 6993-7015
Prospects and limitations of full-text index structures in genome analysis
The combination of incessant advances in sequencing technology producing large amounts of data and innovative bioinformatics approaches, designed to cope with this data flood, has led to new interesting results in the life sciences. Given the magnitude of sequence data to be processed, many bioinformatics tools rely on efficient solutions to a variety of complex string problems. These solutions include fast heuristic algorithms and advanced data structures, generally referred to as index structures. Although the importance of index structures is generally known to the bioinformatics community, the design and potency of these data structures, as well as their properties and limitations, are less understood. Moreover, the last decade has seen a boom in the number of variant index structures featuring complex and diverse memory-time trade-offs. This article brings a comprehensive state-of-the-art overview of the most popular index structures and their recently developed variants. Their features, interrelationships, the trade-offs they impose, but also their practical limitations, are explained and compared.
- 12 May 2012
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 40 (15) , 6993-7015
Open AccessProspects and limitations of full-text index structures in genome analysis
The combination of incessant advances in sequencing technology producing large amounts of data and innovative bioinformatics approaches, designed to cope with this data flood, has led to new interesting results in the life sciences. Given the magnitude of sequence data to be processed, many bioinformatics tools rely on efficient solutions to a variety of complex string problems. These solutions include fast heuristic algorithms and advanced data structures, generally referred to as index structures. Although the importance of index structures is generally known to the bioinformatics community, the design and potency of these data structures, as well as their properties and limitations, are less understood. Moreover, the last decade has seen a boom in the number of variant index structures featuring complex and diverse memory-time trade-offs. This article brings a comprehensive state-of-the-art overview of the most popular index structures and their recently developed variants. Their features, interrelationships, the trade-offs they impose, but also their practical limitations, are explained and compared.