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Nicholas J. Dimonaco

Researcher at Aberystwyth University

Publications -  9
Citations -  49

Nicholas J. Dimonaco is an academic researcher from Aberystwyth University. The author has contributed to research in topics: Biology & Gene. The author has an hindex of 2, co-authored 5 publications receiving 19 citations.

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DeepViral: prediction of novel virus-host interactions from protein sequences and infectious disease phenotypes.

TL;DR: DeepViral as discussed by the authors embeds human proteins and viruses in a shared space using their associated phenotypes and functions, supported by formalized background knowledge from biomedical ontologies, and predicts protein-protein interactions (PPI) between humans and viruses.
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Computational Analysis of SARS-CoV-2 and SARS-Like Coronavirus Diversity in Human, Bat and Pangolin Populations.

TL;DR: In this paper, the authors employed a collection of contemporary methodologies to compare the genomic sequences of coronaviruses isolated from human (SARS-CoV-2; n = 163), bat (bat-coV; n ≥ 215), and pangolin (pangolin-CoVs; n= 7) available in public repositories.
Posted ContentDOI

DeepViral: infectious disease phenotypes improve prediction of novel virus–host interactions

TL;DR: DeepViral is developed, a deep learning based method that predicts protein–protein interactions (PPI) between humans and viruses that significantly improves over existing sequence-based methods for intra- and inter-species PPI prediction.
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Uncovering the dark matter of the metagenome one read at a time

TL;DR: DeepGO is modified to perform protein function prediction directly from sequence reads with limited protein coding sequence prediction, and evaluated the functions predicted from the unassembled sequence reads and the protein coding sequences predicted fromThe assembled metagenome.
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Automated pseudogene detection reveals insights into historical gene sharing dynamics in prokaryotes

TL;DR: StORF-R is presented, a tool that takes as input an annotated genome and returns putative missed genes (functional and/or pseudogenised) from the intergenic regions and shows that this methodology can recover gene-families that the state-of-the-art methods continue to misreport or completely omit.