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FATHMM-XF: accurate prediction of pathogenic point mutations via extended features

Bioinformatics, 2018-02, Vol.34 (3), p.511-513

2018

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An integrative approach to predicting the functional effects of non-coding and coding sequence variation

Bioinformatics, 2015-05, Vol.31 (10), p.1536-1543

2015

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Prediction of driver variants in the cancer genome via machine learning methodologies

Briefings in bioinformatics, 2021-07, Vol.22 (4)

2021

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SpliceGrapher: detecting patterns of alternative splicing from RNA-Seq data in the context of gene models and EST data

Genome biology, 2012-01, Vol.13 (1), p.R4-R4

2012

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Nucleotide diversity of functionally different groups of immune response genes in Old World camels based on newly annotated and reference-guided assemblies

BMC genomics, 2020-09, Vol.21 (1), p.606-606, Article 606

2020

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Corticosterone pattern-dependent glucocorticoid receptor binding and transcriptional regulation within the liver

PLoS genetics, 2021-08, Vol.17 (8), p.e1009737-e1009737

2021

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An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome

BMC bioinformatics, 2017-10, Vol.18 (1), p.442-8, Article 442

2017

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Treating the placenta to prevent adverse effects of gestational hypoxia on fetal brain development

Scientific reports, 2017-08, Vol.7 (1), p.9079-9079, Article 9079

2017

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Deciphering the plant splicing code: experimental and computational approaches for predicting alternative splicing and splicing regulatory elements

Frontiers in plant science, 2012-01, Vol.3, p.18-18

2012

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Genome-wide analysis of alternative splicing in Chlamydomonas reinhardtii

BMC genomics, 2010-02, Vol.11 (1), p.114-114, Article 114

2010

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CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome

Bioinformatics, 2020-06, Vol.36 (12), p.3637-3644

2020

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CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome

Bioinformatics (Oxford, England), 2021-11, Vol.37 (22), p.4298-4298

2021

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CScape: a tool for predicting oncogenic single-point mutations in the cancer genome

Scientific reports, 2017-09, Vol.7 (1), p.11597-10, Article 11597

2017

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Preeclamptic placentae release factors that damage neurons: implications for foetal programming of disease

Neuronal signaling, 2018-12, Vol.2 (4), p.NS20180139-NS20180139

2018

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HIPred: an integrative approach to predicting haploinsufficient genes

Bioinformatics (Oxford, England), 2017-06, Vol.33 (12), p.1751-1757

2017

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Glucocorticoid Receptor-Tethered Mineralocorticoid Receptors Increase Glucocorticoid-Induced Transcriptional Responses

Endocrinology (Philadelphia), 2019-05, Vol.160 (5), p.1044-1056

2019

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Improving Illumina assemblies with Hi‐C and long reads: An example with the North African dromedary

Molecular ecology resources, 2019-07, Vol.19 (4), p.1015-1026

2019

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The use of gene ontology evidence codes in preventing classifier assessment bias

Bioinformatics, 2009-05, Vol.25 (9), p.1173-1177

2009

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Estimating the Frequency of Single Point Driver Mutations across Common Solid Tumours

Scientific reports, 2019-09, Vol.9 (1), p.13452-11, Article 13452

2019

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Recognition memory-induced gene expression in the perirhinal cortex: A transcriptomic analysis

Behavioural brain research, 2017-06, Vol.328, p.1-12

2017

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GTB - an online genome tolerance browser

BMC bioinformatics, 2017-01, Vol.18 (1), p.20-20, Article 20

2017

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Sex‐specific differences in cardiovascular and metabolic hormones with integrated signalling in the paraventricular nucleus of the hypothalamus

Experimental physiology, 2017-11, Vol.102 (11), p.1373-1379

2017

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Probabilistic Inference of Biological Networks via Data Integration

BioMed research international, 2015-01, Vol.2015, p.707453-9

2015

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Differential aging‐related changes in neurophysiology and gene expression in IB4‐positive and IB4‐negative nociceptive neurons

Aging cell, 2018-08, Vol.17 (4), p.e12795-n/a

2018

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Genetic interactions derived from high-throughput phenotyping of 6589 yeast cell cycle mutants

NPJ systems biology and applications, 2020-05, Vol.6 (1), p.11-11, Article 11

2020

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FATHMM-XF: accurate prediction of pathogenic point mutations via extended features

An integrative approach to predicting the functional effects of non-coding and coding sequence variation

Prediction of driver variants in the cancer genome via machine learning methodologies

SpliceGrapher: detecting patterns of alternative splicing from RNA-Seq data in the context of gene models and EST data

Nucleotide diversity of functionally different groups of immune response genes in Old World camels based on newly annotated and reference-guided assemblies

Corticosterone pattern-dependent glucocorticoid receptor binding and transcriptional regulation within the liver

An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome

Treating the placenta to prevent adverse effects of gestational hypoxia on fetal brain development

Deciphering the plant splicing code: experimental and computational approaches for predicting alternative splicing and splicing regulatory elements

Genome-wide analysis of alternative splicing in Chlamydomonas reinhardtii

CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome

CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome

CScape: a tool for predicting oncogenic single-point mutations in the cancer genome

Preeclamptic placentae release factors that damage neurons: implications for foetal programming of disease

HIPred: an integrative approach to predicting haploinsufficient genes

Glucocorticoid Receptor-Tethered Mineralocorticoid Receptors Increase Glucocorticoid-Induced Transcriptional Responses

Improving Illumina assemblies with Hi‐C and long reads: An example with the North African dromedary

The use of gene ontology evidence codes in preventing classifier assessment bias

Estimating the Frequency of Single Point Driver Mutations across Common Solid Tumours

Recognition memory-induced gene expression in the perirhinal cortex: A transcriptomic analysis

GTB - an online genome tolerance browser

Sex‐specific differences in cardiovascular and metabolic hormones with integrated signalling in the paraventricular nucleus of the hypothalamus

Probabilistic Inference of Biological Networks via Data Integration

Differential aging‐related changes in neurophysiology and gene expression in IB4‐positive and IB4‐negative nociceptive neurons

Genetic interactions derived from high-throughput phenotyping of 6589 yeast cell cycle mutants

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