Evidence map›Paper›PMID 42818593›Full record

ArticleBioinformatics advances2026

SHISMA: SHape-driven inference of significant cell type-specific subnetworks from tiMe series single-cell trAnscriptomics.

Antonio Collesei, Pierangela Palmerini, Emilia Vigolo, Francesco Spinnato

Abstract read
In one paragraph

Article in Bioinformatics advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Antonio ColleseiBiostatistics and Bioinformatics, Veneto Institute of Oncology IOV-IRCCS, via Gattamelata 64, Padua, 35128, Italy.ORCID https://orcid.org/0000-0002-5815-7081
Pierangela PalmeriniImmunology and Molecular Oncology Diagnostics, Veneto Institute of Oncology IOV-IRCCS, via Gattamelata 64, Padua, 35128, Italy.
Emilia VigoloImmunology and Molecular Oncology Diagnostics, Veneto Institute of Oncology IOV-IRCCS, via Gattamelata 64, Padua, 35128, Italy.
Francesco SpinnatoDepartment of Computer Science, University of Pisa, Largo Bruno Pontecorvo 3, Pisa, 56127, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Recent advances in DNA and RNA sequencing technologies and the gradual decrease in costs have allowed to design serial experiments with timestamps, even at single cell resolution. This possibility unlocks a finer level of detail, as well as a huge amount of noisy information to decode. Tools inferring regulatory networks, or patterns, from this type of data often focus on trajectories, disregarding local shapes and fundamental time series primitives. Moreover, they fail to target the analysis on a few meaningful results, reporting large and noisy outputs that need further downstream analysis. Results: We describe SHISMA, a novel tool to infer significant cell type-specific co-dynamic gene subnetworks, from time series transcriptomic data, with strong statistical guarantees in terms of Availability and implementation: https://github.com/antoniocollesei/SHISMA.

Identifiers

PMID42818593
PMCPMC13623514

What Socratic holds

Textmetadata
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Registered trials

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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.