Tom R. Gaunt

According to our database1, Tom R. Gaunt authored at least 18 papers between 2006 and 2018.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

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Bibliography

2018
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.
Bioinform., 2018

2017
GTB - an online genome tolerance browser.
BMC Bioinform., 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

HIPred: an integrative approach to predicting haploinsufficient genes.
Bioinform., 2017

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
BioData Min., 2017

2015
Texture classification using feature selection and kernel-based techniques.
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
Canonical Correlation Analysis for Gene-Based Pleiotropy Discovery.
PLoS Computational Biology, 2014

A pathway-based data integration framework for prediction of disease progression.
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

A Random Forest proximity matrix as a new measure for gene annotation.
Proceedings of the 22th European Symposium on Artificial Neural Networks, 2014

2013
Predicting the functional consequences of cancer-associated amino acid substitutions.
Bioinform., 2013

Texture Classification Using Kernel-Based Techniques.
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


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