Literature DB >> 32570509

Text-Mining Services of the Swiss Variant Interpretation Platform for Oncology.

Déborah Caucheteur1,2, Julien Gobeill1,2, Anaïs Mottaz1,2, Emilie Pasche1,2, Pierre-André Michel1,2, Luc Mottin1,2, Daniel J Stekhoven2,3, Valérie Barbié2, Patrick Ruch1,2.   

Abstract

The Swiss Variant Interpretation Platform for Oncology is a centralized, joint and curated database for clinical somatic variants piloted by a board of Swiss healthcare institutions and operated by the SIB Swiss Institute of Bioinformatics. To support this effort, SIB Text Mining designed a set of text analytics services. This report focuses on three of those services. First, the automatic annotations of the literature with a set of terminologies have been performed, resulting in a large annotated version of MEDLINE and PMC. Second, a generator of variant synonyms for single nucleotide variants has been developed using publicly available data resources, as well as patterns of non-standard formats, often found in the literature. Third, a literature ranking service enables to retrieve a ranked set of MEDLINE abstracts given a variant and optionally a diagnosis. The annotation of MEDLINE and PMC resulted in a total of respectively 785,181,199 and 1,156,060,212 annotations, which means an average of 26 and 425 annotations per abstract and full-text article. The generator of variant synonyms enables to retrieve up to 42 synonyms for a variant. The literature ranking service reaches a precision (P10) of 63%, which means that almost two-thirds of the top-10 returned abstracts are judged relevant. Further services will be implemented to complete this set of services, such as a service to retrieve relevant clinical trials for a patient and a literature ranking service for full-text articles.

Entities:  

Keywords:  Precision medicine; literature; terminology; text-mining; variant

Year:  2020        PMID: 32570509     DOI: 10.3233/SHTI200288

Source DB:  PubMed          Journal:  Stud Health Technol Inform        ISSN: 0926-9630


  1 in total

1.  Variomes: a high recall search engine to support the curation of genomic variants.

Authors:  Emilie Pasche; Anaïs Mottaz; Déborah Caucheteur; Julien Gobeill; Pierre-André Michel; Patrick Ruch
Journal:  Bioinformatics       Date:  2022-03-11       Impact factor: 6.931

  1 in total

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