Tom R. Gaunt
Orcid: 0000-0003-0924-3247
According to our database1,
Tom R. Gaunt
authored at least 28 papers
between 2006 and 2024.
Collaborative distances:
Collaborative distances:
Timeline
2006
2008
2010
2012
2014
2016
2018
2020
2022
2024
0
1
2
3
4
5
6
7
1
2
6
1
1
6
2
2
1
1
1
1
2
1
Legend:
Book In proceedings Article PhD thesis Dataset OtherLinks
Online presence:
-
on orcid.org
On csauthors.net:
Bibliography
2024
2023
J. Big Data, December, 2023
Using language models and ontology topology to perform semantic mapping of traits between biomedical datasets.
Bioinform., April, 2023
2021
An informatics consult approach for generating clinical evidence for treatment decisions.
BMC Medical Informatics Decis. Mak., 2021
MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes.
Bioinform., 2021
Bioinform., 2021
Bioinform., 2021
MELODI Presto: a fast and agile tool to explore semantic triples derived from biomedical literature.
Bioinform., 2021
Prediction of driver variants in the cancer genome via machine learning methodologies.
Briefings Bioinform., 2021
2020
CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome.
Bioinform., 2020
2018
Bioinform., 2018
2017
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.
BMC Bioinform., 2017
HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics.
Bioinform., 2017
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.
Bioinform., 2017
Bioinform., 2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
BioData Min., 2017
2015
Soft Comput., 2015
An integrative approach to predicting the functional effects of non-coding and coding sequence variation.
Bioinform., 2015
Sequential data selection for predicting the pathogenic effects of sequence variation.
Proceedings of the 2015 IEEE International Conference on Bioinformatics and Biomedicine, 2015
2014
PLoS Comput. Biol., 2014
Bioinform., 2014
Using a Random Forest proximity measure for variable importance stratification in genotypic data.
Proceedings of the International Work-Conference on Bioinformatics and Biomedical Engineering, 2014
Proceedings of the 22th European Symposium on Artificial Neural Networks, 2014
2013
Predicting the functional consequences of cancer-associated amino acid substitutions.
Bioinform., 2013
Proceedings of the Advances in Computational Intelligence, 2013
2007
Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'.
BMC Bioinform., 2007
2006
MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers.
BMC Bioinform., 2006