Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Tanja Kunej

dblp:190/6940 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
1since 2021 · last 2021
0000-0002-0465-1762ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 1 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › network bioinformatics › biological network analysis › network analysis
causal network analysis
0.512021
CaNDis: a web server for investigation of causal relationships between diseases, drugs and drug targets · Bioinform. 2021

Methods — techniques the papers use, named apart from their topics

causal interaction network fusion · 0.5
YearPublicationVenuePosition
2021 CaNDis: a web server for investigation of causal relationships between diseases, drugs and drug targets
abstract
MOTIVATION: Causal biological interaction networks represent cellular regulatory pathways. Their fusion with other biological data enables insights into disease mechanisms and novel opportunities for drug discovery. RESULTS: We developed Causal Network of Diseases (CaNDis), a web server for the exploration of a human causal interaction network, which we expanded with data on diseases and FDA-approved drugs, on the basis of which we constructed a disease-disease network in which the links represent the similarity between diseases. We show how CaNDis can be used to identify candidate genes with known and novel roles in disease co-occurrence and drug-drug interactions. AVAILABILITYAND IMPLEMENTATION: CaNDis is freely available to academic users at http://candis.ijs.si and http://candis.insilab.org. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Blaz Skrlj, Nika Erzen, Nada Lavrac, Tanja Kunej, Janez Konc
Bioinform.4