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E. Nikitin

dblp:436/5109 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2026
—ORCID · none

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 4 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
biomarker discovery
1.012026
Nested co-expression network analysis identifies compact gene clusters in a black box · Bioinform. 2026
Bioinformatics and computational biology › network bioinformatics › biological network analysis
gene co-expression network analysis
1.012026
Nested co-expression network analysis identifies compact gene clusters in a black box · Bioinform. 2026
Bioinformatics and computational biology
gene expression analysis
1.012026
Nested co-expression network analysis identifies compact gene clusters in a black box · Bioinform. 2026
Bioinformatics and computational biology › biomarker discovery
prognostic biomarker identification
1.012026
Nested co-expression network analysis identifies compact gene clusters in a black box · Bioinform. 2026

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

weighted gene co-expression network analysis · 1.0unsupervised clustering · 1.0
YearPublicationVenuePosition
2026 Nested co-expression network analysis identifies compact gene clusters in a black box
abstract
MOTIVATION: Digital analysis of biological systems requires methods capable of identifying both broad and nested gene modules reflecting complex biological processes. Existing transcriptomic methods often miss compact gene sets corresponding to subprocesses in specialized cell types, limiting insights into functional heterogeneity. RESULTS: We present Nested-WGCNA, a two-stage unsupervised network analysis algorithm designed to identify coarse-grained and fine-grained gene modules. Applied to bulk RNA-Seq data, Nested-WGCNA reveals stable modules reproducible across datasets. When validated against scRNA-Seq data, these modules correspond to both major and minor immune cell subtypes. Application to immunotherapy response datasets uncovers predictive and prognostic biomarkers, highlighting its utility in treatment stratification and biomarker discovery. AVAILABILITY: The NestedWGCNA source code and analysis pipeline are available on GitHub (https://github.com/ilyada/NestedWGCNA) and archived on Zenodo (https://doi.org/10.5281/zenodo.18959244).
I. A. Dyugay, Aleksandr Poslavsky, Daniil K. Lukyanov, F. M. Polyakov, E. Nikitin, E. Klimuk, A. Dakhnovets, Denis Syrko, Victor V. Kotliar, Dmitry Chudakov
Bioinform.5