Bjarni V. Halldórsson
Orcid: 0000-0003-0756-0767
According to our database1,
Bjarni V. Halldórsson
authored at least 41 papers
between 2001 and 2024.
Collaborative distances:
Collaborative distances:
Timeline
Legend:
Book In proceedings Article PhD thesis Dataset OtherLinks
Online presence:
-
on zbmath.org
-
on orcid.org
On csauthors.net:
Bibliography
2024
Bioinform., 2024
2023
Bioinform., August, 2023
2022
Population-scale detection of non-reference sequence variants using colored de Bruijn graphs.
Bioinform., 2022
2021
Local improvement algorithms for a path packing problem: A performance analysis based on linear programming.
Oper. Res. Lett., 2021
read_haps: using read haplotypes to detect same species contamination in DNA sequences.
Bioinform., 2021
2020
Bioinform., 2020
2019
Clinical decision support system for the management of osteoporosis compared to NOGG guidelines and an osteology specialist: a validation pilot study.
BMC Medical Informatics Decis. Mak., 2019
A Branch & Price algorithm for the minimum cost clique cover problem in max-point tolerance graphs.
4OR, 2019
2017
Corrigendum to "A Clinical Decision Support System for the Diagnosis, Fracture Risks and Treatment of Osteoporosis".
Comput. Math. Methods Medicine, 2017
2016
2015
A Clinical Decision Support System for the Diagnosis, Fracture Risks and Treatment of Osteoporosis.
Comput. Math. Methods Medicine, 2015
2014
Bioinform., 2014
Proceedings of the Combinatorial Optimization and Applications, 2014
2013
An Integer Programming Formulation of the Parsimonious Loss of Heterozygosity Problem.
IEEE ACM Trans. Comput. Biol. Bioinform., 2013
Algorithms Mol. Biol., 2013
2012
DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism.
Bioinform., 2012
A Mixed Integer Programming Model for the Parsimonious Loss of Heterozygosity Problem.
Proceedings of the Bioinformatics Research and Applications - 8th International Symposium, 2012
Proceedings of the IEEE 2nd International Conference on Computational Advances in Bio and Medical Sciences, 2012
2011
An Algorithm for Detecting High Frequency Copy Number Polymorphisms Using SNP Arrays.
J. Comput. Biol., 2011
The Clark Phaseable Sample Size Problem: Long-Range Phasing and Loss of Heterozygosity in GWAS.
J. Comput. Biol., 2011
Haplotype Phasing By Multi-Assembly of Shared Haplotypes: Phase-Dependent Interactions Between Rare Variants.
Proceedings of the Biocomputing 2011: Proceedings of the Pacific Symposium, 2011
2010
The Clark Phase-able Sample Size Problem: Long-Range Phasing and Loss of Heterozygosity in GWAS.
Proceedings of the Research in Computational Molecular Biology, 2010
Proceedings of the Automata, Languages and Programming, 37th International Colloquium, 2010
2009
Proceedings of the Developments in Language Theory, 13th International Conference, 2009
2006
IEEE ACM Trans. Comput. Biol. Bioinform., 2006
J. Comput. Biol., 2006
2003
Proceedings of the Sventh Annual International Conference on Computational Biology, 2003
Proceedings of the Discrete Mathematics and Theoretical Computer Science, 2003
Proceedings of the 2nd IEEE Computer Society Bioinformatics Conference, 2003
2002
Proceedings of the Computational Methods for SNPs and Haplotype Inference, 2002
2001
Proceedings of the Algorithms, 2001