Evidence map›Paper›PMID 41114645›Full record

ArticleGigaScience2025

Reproducible processing of TCGA regulatory networks.

Viola Fanfani, Katherine H Shutta, Panagiotis Mandros, Jonas Fischer, Enakshi Saha, Soel Micheletti, Chen Chen, Marouen Ben Guebila, Camila M Lopes-Ramos, John Quackenbush

Abstract read
In one paragraph

Article in GigaScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Viola FanfaniDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0003-3852-6908
Katherine H ShuttaDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0003-0402-3771
Panagiotis MandrosDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0009-0008-9638-9722
Jonas FischerDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0002-6459-5053
Enakshi SahaDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0003-2938-539X
Soel MichelettiDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0001-5402-9237
Chen ChenDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0002-8042-7201
Marouen Ben GuebilaDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0001-5934-966X
Camila M Lopes-RamosDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0003-0284-7371
John QuackenbushDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115  USA.ORCID 0000-0002-2702-5879

Funding

Tissue and Pathology ResourcesP50CA127003 · NCI · DANA-FARBER CANCER INST · PI SHIVDASANI, RAMESH A · 2007 to 2023
$33.2M
Respiratory Computational Discovery CoreP01HL114501 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ELIAS, JACK A · 2013 to 2025
$24.9M
SYSTEMS APPROACHES TO THE EPIDEMIOLOGY, GENETICS AND GENOMICS OF LUNG DISEASEST32HL007427 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI DAWN L DEMEO, Edwin K Silverman · 1985 to 2026
$13.6M
Unraveling the Complexities of Risk and Mechanism in CancerR35CA220523 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI QUACKENBUSH, JOHN · 2018 to 2024
$6.0M
WebMeV: A Robust Platform for Intuitive Genomic Data AnalysisU24CA231846 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI QUACKENBUSH, JOHN · 2019 to 2023
$3.2M
Networks Tools to Understand Sex- and Gender-Specific Drivers of DiseaseR01HG011393 · NHGRI · BRIGHAM AND WOMEN'S HOSPITAL · PI DEMEO, DAWN L, QUACKENBUSH, JOHN · 2021 to 2024
$2.1M
Sex chromosome gene regulatory networks and COPDK01HL166376 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LOPES-RAMOS, CAMILA · 2023 to 2024
$324k
National Human Genone Research Institute P01HL114501National Human Genone Research Institute T32HL007427NCI NIH HHS P50 CA127003NCI NIH HHS P50CA127003NCI NIH HHS R01HG011393NCI NIH HHS R35 CA220523NCI NIH HHS U24 CA231846NCI NIH HHS U24CA231846NHGRI NIH HHS R01 HG011393NHLBI NIH HHS K01 HL166376NHLBI NIH HHS K01HL166376NHLBI NIH HHS LCD-821824NHLBI NIH HHS P01 HL114501NHLBI NIH HHS T32 HL007427NIH HHS R35CA220523
6 · The paper itself

Abstract

backgroundTechnological advances in sequencing and computation have allowed deep exploration of the molecular basis of diseases. Biological networks have proven to be a valuable framework for analyzing omics data and modeling regulatory interactions between genes and proteins. Large collaborative projects, such as The Cancer Genome Atlas (TCGA), have provided a rich resource for building and validating new computational methods, resulting in a plethora of open-source software for downloading, preprocessing, and analyzing those data. However, for an end-to-end analysis of regulatory networks, a coherent and reusable workflow is essential to integrate all relevant packages into a robust pipeline.

findingsWe developed tcga-data-nf, a Nextflow workflow that allows users to reproducibly infer regulatory networks from the thousands of samples in TCGA using a single command. The workflow can be divided into 3 main steps: multiomic data, such as RNA sequencing and methylation, are (i) downloaded, (ii) preprocessed, and (iii) analyzed to infer regulatory network models with the Network Zoo. The workflow is powered by the NetworkDataCompanion R package, a standalone collection of functions for managing, mapping, and filtering TCGA data. Here, we demonstrate how the pipeline can be used to investigate the differences between colon cancer subtypes attributed to epigenetic mechanisms. Lastly, we provide a database of pregenerated networks for the 10 most common cancer types that can be readily accessed by the public.

conclusionstcga-data-nf is a complete, yet flexible and extensible, framework that enables the reproducible inference and analysis of cancer regulatory networks, bridging a gap in the current universe of software tools for analyzing TCGA data.

Indexed as

Computational BiologyGene Regulatory NetworksNeoplasmsDatabases, GeneticHumansSoftwareWorkflowcancergene regulatory networkNetworkDataCompanionNextflowreproducibilityThe Cancer Genome Atlas

Identifiers

PMID41114645
PMCPMC12720619

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.