Author

Antonio Jimeno Yepes

IBM Research - AustraliaORCID 0000-0002-6581-094XUnclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Antonio Jimeno Yepes1 paper · RMIT University

Biology Disciplines

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Bioinformatics· 2

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:database / resource· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andrew MacKinlayiD· 1 shared Benjamin GoudeyiD· 1 shared Christine Schieber· 1 shared David MartíneziD· 1 shared Matthew T. DowntoniD· 1 shared Natalie GunniD· 1 shared Noel Garry FauxiD· 1 shared Pieter BarnardiD· 1 shared

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2018-2021 · peak 1/yr

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10 top collaborators · 24 mutual co-author links

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1 shared paperBioinformatics

Andrew MacKinlayORCID

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2 papers

Recent·Most cited

BioinformaticsbioRxivPreprintMay 10, 2021

A corpus for differential diagnosis: an eye diseases use case

Antonio Jimeno Yepes, David Martínez, Pieter Barnard, Tinu Theckel Joy

The paper creates a corpus for extracting diagnostic information from eye disease literature, showing strong agreement in entity annotation and potential for new insights using BioBERT.

DOI 10.1101/2021.05.10.443343

statistical modeldatabase / resource

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BioinformaticsbioRxivPreprintJul 6, 2018

A hybrid approach for automated mutation annotation of the extended human mutation landscape in scientific literature

Antonio Jimeno Yepes, Andrew MacKinlay, Natalie Gunn…·Richard L. Martin

This paper introduces an automated mutation annotator that covers an extended mutation landscape, achieving F1 performance comparable to human annotation.

6 citations

humanwhole-genome sequencing

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