PredictONCO: A web tool supporting decision-making in precision oncology by extending the bioinformatics predictions with advanced computing and machine learning
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F23%3A00079453" target="_blank" >RIV/65269705:_____/23:00079453 - isvavai.cz</a>
Alternative codes found
RIV/00159816:_____/24:00079453 RIV/00216224:14310/24:00135293
Result on the web
<a href="https://academic.oup.com/bib/article/25/1/bbad441/7463300" target="_blank" >https://academic.oup.com/bib/article/25/1/bbad441/7463300</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1093/bib/bbad441" target="_blank" >10.1093/bib/bbad441</a>
Alternative languages
Result language
angličtina
Original language name
PredictONCO: A web tool supporting decision-making in precision oncology by extending the bioinformatics predictions with advanced computing and machine learning
Original language description
PredictONCO 1.0 is a unique web server that analyzes effects of mutations on proteins frequently altered in various cancer types. The server can assess the impact of mutations on the protein sequential and structural properties and apply a virtual screening to identify potential inhibitors that could be used as a highly individualized therapeutic approach, possibly based on the drug repurposing. PredictONCO integrates predictive algorithms and state-of-the-art computational tools combined with information from established databases. The user interface was carefully designed for the target specialists in precision oncology, molecular pathology, clinical genetics and clinical sciences. The tool summarizes the effect of the mutation on protein stability and function and currently covers 44 common oncological targets. The binding affinities of Food and Drug Administration/ European Medicines Agency -approved drugs with the wild-type and mutant proteins are calculated to facilitate treatment decisions. The reliability of predictions was confirmed against 108 clinically validated mutations. The server provides a fast and compact output, ideal for the often time-sensitive decision-making process in oncology. Three use cases of missense mutations, (i) K22A in cyclin-dependent kinase 4 identified in melanoma, (ii) E1197K mutation in anaplastic lymphoma kinase 4 identified in lung carcinoma and (iii) V765A mutation in epidermal growth factor receptor in a patient with congenital mismatch repair deficiency highlight how the tool can increase levels of confidence regarding the pathogenicity of the variants and identify the most effective inhibitors. The server is available at https://loschmidt.chemi.muni.cz/predictonco.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10609 - Biochemical research methods
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Briefings in Bioinformatics
ISSN
1467-5463
e-ISSN
1477-4054
Volume of the periodical
25
Issue of the periodical within the volume
1
Country of publishing house
US - UNITED STATES
Number of pages
10
Pages from-to
"bbad441"
UT code for WoS article
001173375300096
EID of the result in the Scopus database
2-s2.0-85180282604