Evidence map›Paper›PMID 42063826›Full record

ArticleJACS Au2026

CLaSSiNet: A Computational Framework for High-Resolution Classification and Spatial Mapping of Heterogeneous Biological Network Architectures.

Yuan Tao, Ruobo Zhou

Abstract read
In one paragraph

Article in JACS Au, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Yuan TaoDepartment of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.ORCID https://orcid.org/0000-0002-6026-9584
Ruobo ZhouDepartment of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.ORCID https://orcid.org/0000-0001-8628-0282

Funding

Deciphering the functional role of actin-spectrin-based membrane skeleton in subcellular compartmentalization of signaling proteins and cell signal transductionR35GM142973 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI ZHOU, RUOBO · 2021 to 2025
$2.2M
NIGMS NIH HHS R35 GM142973
6 · The paper itself

Abstract

Quantitative analysis of network-like biological molecular architectures, such as cytoskeletal networks, remains a fundamental challenge in super-resolution fluorescence imaging because single-molecule localization microscopy (SMLM) typically produces sparse and discontinuous localization patterns arising from stochastic labeling, incomplete probe occupancy, and structural deformation of biological networks. These factors obscure the underlying connectivity, periodicity, and symmetry, limiting the ability of existing analysis methods to resolve higher-order organization. Here, we report the Classifier of Super-resolution Structural Networks (

Indexed as

CytoskeletonImage AnalysisMembrane-Associated Periodic Skeleton (MPS)Network TopologySingle-Molecule Localization Microscopy (SMLM)Structural Organization ClassificationSuper-Resolution Imaging

Identifiers

PMID42063826
PMCPMC13126174

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.