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1.
Brief Bioinform ; 23(1)2022 01 17.
Artigo em Inglês | MEDLINE | ID: mdl-34472587

RESUMO

Chemosensitivity assays are commonly used for preclinical drug discovery and clinical trial optimization. However, data from independent assays are often discordant, largely attributed to uncharacterized variation in the experimental materials and protocols. We report here the launching of Minimal Information for Chemosensitivity Assays (MICHA), accessed via https://micha-protocol.org. Distinguished from existing efforts that are often lacking support from data integration tools, MICHA can automatically extract publicly available information to facilitate the assay annotation including: 1) compounds, 2) samples, 3) reagents and 4) data processing methods. For example, MICHA provides an integrative web server and database to obtain compound annotation including chemical structures, targets and disease indications. In addition, the annotation of cell line samples, assay protocols and literature references can be greatly eased by retrieving manually curated catalogues. Once the annotation is complete, MICHA can export a report that conforms to the FAIR principle (Findable, Accessible, Interoperable and Reusable) of drug screening studies. To consolidate the utility of MICHA, we provide FAIRified protocols from five major cancer drug screening studies as well as six recently conducted COVID-19 studies. With the MICHA web server and database, we envisage a wider adoption of a community-driven effort to improve the open access of drug sensitivity assays.

2.
bioRxiv ; 2021 Jun 12.
Artigo em Inglês | MEDLINE | ID: mdl-33300000

RESUMO

Chemosensitivity assays are commonly used for preclinical drug discovery and clinical trial optimization. However, data from independent assays are often discordant, largely attributed to uncharacterized variation in the experimental materials and protocols. We report here the launching of MICHA (Minimal Information for Chemosensitivity Assays), accessed via https://micha-protocol.org. Distinguished from existing efforts that are often lacking support from data integration tools, MICHA can automatically extract publicly available information to facilitate the assay annotation including: 1) compounds, 2) samples, 3) reagents, and 4) data processing methods. For example, MICHA provides an integrative web server and database to obtain compound annotation including chemical structures, targets, and disease indications. In addition, the annotation of cell line samples, assay protocols and literature references can be greatly eased by retrieving manually curated catalogues. Once the annotation is complete, MICHA can export a report that conforms to the FAIR principle (Findable, Accessible, Interoperable and Reusable) of drug screening studies. To consolidate the utility of MICHA, we provide FAIRified protocols from five major cancer drug screening studies, as well as six recently conducted COVID-19 studies. With the MICHA webserver and database, we envisage a wider adoption of a community-driven effort to improve the open access of drug sensitivity assays.

3.
Ecol Evol ; 11(21): 14344-14350, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34765110

RESUMO

Author-level metrics are a widely used measure of scientific success. The h-index and its variants measure publication output (number of publications) and research impact (number of citations). They are often used to influence decisions, such as allocating funding or jobs. Here, we argue that the emphasis on publication output and impact hinders scientific progress in the fields of ecology and evolution because it disincentivizes two fundamental practices: generating impactful (and therefore often long-term) datasets and sharing data. We describe a new author-level metric, the data-index, which values both dataset output (number of datasets) and impact (number of data-index citations), so promotes generating and sharing data as a result. We discuss how it could be implemented and provide user guidelines. The data-index is designed to complement other metrics of scientific success, as scientific contributions are diverse and our value system should reflect that both for the benefit of scientific progress and to create a value system that is more equitable, diverse, and inclusive. Future work should focus on promoting other scientific contributions, such as communicating science, informing policy, mentoring other scientists, and providing open-access code and tools.

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