OSCR

Systematic fMRI signal differences across cohorts alter lifespan trajectories of functional brain networks.

Code ↔ Paper

2 matches between paragraphs of the paper and lines of its authors' code, computed by the harvester (lexical-v1). Click a colored paragraph or line to see its counterpart.

The 2 matches
  1. [1] § Methods › Data harmonization ↔ R/R/combat.R, lines 12–70 · score 0.52 · batch factor, ComBat, variance, harmonization, covariates, model
  2. [2] § Methods › Data harmonization ↔ R/R/covbat.R, lines 11–80 · score 0.51 · CovBat, ComBat, variance, harmonization, covariates, model

Paper

Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC

The paper is loaded when this pane is shown.

The authors' code

R · 220 lines · 8.4 KB · no license · 1 match

The registry keeps no copy of this file: its repository has no license, so its authors keep all their rights to it. Your browser shows it from its source, with JavaScript.

It can be read at the source: R/R/combat.R.

Overview

  1. Center for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, Dallas, TX, United States
  2. Department of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, TX, United States
Journal: Imaging neuroscience (Cambridge, Mass.), volume 4, article IMAG.a.1338
Dates: received 15 January 2026; accepted 15 July 2026; published online 24 August 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1162/imag.a.1338 · PMID 42643755 · PMCID PMC13504956 · OpenAlex W7171803933
Open access: diamond, a free copy (OpenAlex)
Status: code verified
Categories: fMRI (modality), human (organism), systems (subfield)
Methods: Spectral & time-frequency, Preprocessing, Connectivity, Graphs, fMRI & imaging
Keywords: resting-state functional correlation, brain network, lifespan neuroimaging, data harmonization, human connectome project
MeSH: Aging*, Brain*, Connectome*, Magnetic Resonance Imaging*, Nerve Net*, Adult, Aged, Aged, 80 and over, Cohort Studies, Female, Humans, Longevity, Male, Middle Aged, Signal-To-Noise Ratio, Young Adult (* major topic)
Topic: Functional Brain Connectivity Studies (Cognitive Neuroscience, Neuroscience), according to OpenAlex
Funding: NIA NIH HHS (U01 AG052564, R01 AG092219, R01 AG063930); NIMH NIH HHS (U01 MH109589, U54 MH091657)
Citations: not cited yet (Europe PMC); 62 references in the paper

Abstract

Large-scale lifespan neuroimaging studies increasingly integrate data across distinct cohorts to characterize trajectories of brain development and aging. However, systematic differences in acquisition protocols and hardware across cohorts can alter signal characteristics in ways that bias downstream analyses. Here, we examine three cohorts from the Human Connectome Project (HCP), spanning development (HCP-D), young adulthood (HCP-YA) and aging (HCP-A), to illustrate this issue and evaluate existing strategies to mitigate it. HCP has set standards for open, deeply phenotyped, high-resolution human neuroimaging, which are frequently used as high-quality reference datasets in tool validation, replication studies, and cross-cohort meta-analyses. However, neuroimaging acquisitions have differed across HCP cohorts because of changes in scanner hardware and acquisition sequences across study phases. Because of HCP’s widespread usage, even modest protocol differences between cohorts—and their downstream effects—can have outsized impacts on the field of neuroscience research. Our analysis reveals that the HCP-YA cohort exhibits systematically weaker temporal signal-to-noise ratio (tSNR) relative to HCP-D/A. These signal quality discrepancies propagate to downstream analyses, leading to differences in overall resting-state functional correlations and whole-brain and node-level measures of resting-state network organization (e.g., system segregation, modularity, participation coefficient). Consistent with protocol-driven signal differences, resting-state network measures derived from HCP-YA depart from expected lifespan trajectories, as confirmed by examination of two other lifespan datasets. Harmonization approaches accounting for protocol and scanner-model differences substantially lessen these artifactual differences in brain network measures. Our findings underscore that signal differences do not merely introduce noise, but can qualitatively alter estimated lifespan trajectories of functional network organization, including partially inverting expected lifespan patterns. Without appropriate harmonization, analyses that combine HCP cohorts can therefore result in biologically misleading inferences about brain development and aging. We demonstrate how small acquisition differences bias resting-state-derived network metrics, and how these effects can be mitigated. This work advances best practices for valid inference in multi-cohort lifespan neuroscience research.

Reproduced under the paper's license (CC BY), from the paper cited above.

Repositories

Its files are read in the Code ↔ Paper reader above, with 2 matches between paragraphs and lines of code.

andy1764/CovBat_Harmonization

License: none: the authors keep all their rights
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: cacf370af1ffc87485f50733f797b236c4f251a7, 13 March 2023
Languages: R (4), Python (3)
Size: 25 files, 7 scripts
Software Heritage: not archived
Found in: “Data and Code Availability”
Holds: README, environment (R/DESCRIPTION), documentation
Not found: license file, CITATION.cff, tests, continuous integration
Tools: NumPy (3 files), pandas (3 files), scikit-learn (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
8 files, not copied: shown from their source

OSCR keeps no copy of these files: this repository has no license that allows it. The reader above shows each one from its source, fetched by your browser at commit cacf370, when its fingerprint is the one OSCR verified. How this works.

mychan24/system-segregation-and-graph-tools

License: MIT
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: e7c30345b8ebf29e3a9ab44593d95e41cd0b16ed, 15 October 2024
Languages: MATLAB (11), R (6)
Size: 22 files, 17 scripts
Software Heritage: archived
Found in: “Data and Code Availability”
Holds: README, license file, environment (DESCRIPTION), tests, continuous integration
Not found: CITATION.cff, documentation
Tools: GIfTI library for MATLAB (3 files), cifti-matlab (2 files)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
19 files

The paper's code and data availability statement is in the Data section.

Tracing map

Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.

What the map holds:

  • 2 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 24 scripts, each with its path and the digest of its content;
  • 2 matches between paragraphs of the paper and lines of the code (method lexical-v1);
  • neither the text of the paper nor the code itself.

Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.

Data

Datasets cited

Data and Code Availability

HCP-YA S1200 release data (downloaded March 2023) are available via the Human Connectome Project website (https://www.humanconnectome.org). HCP-D and HCP-A release 2.0 data (downloaded August 2022) are available via the NIMH Data Archive (NDA; https://nda.nih.gov). NKI processed data were downloaded from the NKI-RS repository (S3 bucket). DLBS data are available on OpenNeuro (https://openneuro.org/datasets/ds004856). CovBat was applied using R code available on https://github.com/andy1764/CovBat_Harmonization. RSFC matrix extraction and brain system segregation calculation were completed using code available on https://github.com/mychan24/system-segregation-and-graph-tools. Modularity, participation coefficient, and clustering coefficient were calculated using the Brain Connectivity Toolbox (BCT; https://sites.google.com/site/bctnet).

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, pages, dates, 3 authors, 5 keywords, 16 MeSH terms, 2 funders, 60 references.

Cite

This paper

Chan, M. Y., Han, L., & Wig, G. S. (2026). Systematic fMRI signal differences across cohorts alter lifespan trajectories of functional brain networks. Imaging neuroscience (Cambridge, Mass.), 4, IMAG.a.1338. https://doi.org/10.1162/imag.a.1338

BibTeX

@article{chan2026systematic,
author = {Chan, Micaela Y and Han, Liang and Wig, Gagan S},
title = {{Systematic fMRI signal differences across cohorts alter lifespan trajectories of functional brain networks}},
journal = {Imaging neuroscience (Cambridge, Mass.)},
year = {2026},
month = aug,
volume = {4},
pages = {IMAG.a.1338},
publisher = {MIT Press},
issn = {2837-6056},
doi = {10.1162/imag.a.1338},
url = {https://doi.org/10.1162/imag.a.1338},
pmid = {42643755},
pmcid = {PMC13504956}
}

RIS

TY - JOUR
AU - Chan, Micaela Y
AU - Han, Liang
AU - Wig, Gagan S
TI - Systematic fMRI signal differences across cohorts alter lifespan trajectories of functional brain networks
T2 - Imaging neuroscience (Cambridge, Mass.)
J2 - Imaging Neurosci (Camb)
PY - 2026
DA - 2026/08/24
VL - 4
SP - IMAG.a.1338
SN - 2837-6056
PB - MIT Press
DO - 10.1162/imag.a.1338
UR - https://doi.org/10.1162/imag.a.1338
LA - en
ER -

CSL-JSON

{
"id": "10.1162/imag.a.1338",
"type": "article-journal",
"title": "Systematic fMRI signal differences across cohorts alter lifespan trajectories of functional brain networks",
"container-title": "Imaging neuroscience (Cambridge, Mass.)",
"author": [
{
"family": "Chan",
"given": "Micaela Y"
},
{
"family": "Han",
"given": "Liang"
},
{
"family": "Wig",
"given": "Gagan S"
}
],
"container-title-short": "Imaging Neurosci (Camb)",
"volume": "4",
"page": "IMAG.a.1338",
"DOI": "10.1162/imag.a.1338",
"PMID": "42643755",
"PMCID": "PMC13504956",
"ISSN": "2837-6056",
"publisher": "MIT Press",
"URL": "https://doi.org/10.1162/imag.a.1338",
"language": "en",
"issued": {
"date-parts": [
[
2026,
8,
24
]
]
}
}

The tracing map gets a citation of its own once an author has validated it and it has a DOI.

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1371/journal.pbio.3003856 [code]
Aging and metabolism contribute separately to brain-body health.
Journal: PLoS biology
In common: GIfTI library for MATLAB, scikit-learn, pandas, 1 other tool, humanconnectome.org/study/hcp-lifespan-aging, 9 references
[2] doi:10.1162/imag.a.1285 [code]
Individualized mapping of functional brain networks in older adulthood.
Journal: Imaging neuroscience (Cambridge, Mass.)
In common: cifti-matlab, GIfTI library for MATLAB, systems, fMRI, 8 references
[3] doi:10.21203/rs.3.rs-9326213/v1 [code]
Multi-task fMRI outperforms resting-state fMRI for revealing task-invariant organization of the human brain
Journal: Research Square (preprint)
In common: GIfTI library for MATLAB, scikit-learn, pandas, 1 other tool, humanconnectome.org/study/hcp-young-adult, fMRI, 6 references
[4] doi:10.1038/s41586-026-10454-2 [code]
White matter micro- and macrostructure brain charts for the human lifespan.
Journal: Nature
In common: pandas, NumPy, humanconnectome.org/study/hcp-lifespan-aging, OpenNeuro ds004856, 1 other dataset, 1 reference
[5] doi:10.1016/j.neuron.2026.04.011 [code]
Precision fMRI reveals densely interdigitated network patches with conserved motifs in the lateral prefrontal cortex.
Journal: Neuron
In common: GIfTI library for MATLAB, scikit-learn, NumPy, systems, fMRI, 7 references
[6] doi:10.1186/s40337-026-01671-1 [code]
Aberrant large- and mesoscale network segregation and integration in bulimia nervosa.
Journal: Journal of eating disorders
In common: cifti-matlab, GIfTI library for MATLAB, fMRI, 6 references
[7] doi:10.1038/s42003-026-10282-0 [code]
Genetic risk of Alzheimer's disease is associated with loss of brain network segregation in midlife.
Journal: Communications biology
In common: 9 references
[8] doi:10.1093/oons/kvag006 [code]
Social disconnection in the brain: loneliness and age across networks using graph theory.
Journal: Oxford open neuroscience
In common: pandas, NumPy, fMRI, 8 references
[9] doi:10.1038/s41467-026-73072-6 [code]
Mapping the spatiotemporal continuum of structural connectivity development across the human connectome in youth.
Journal: Nature communications
In common: cifti-matlab, pandas, NumPy, 7 references
[10] doi:10.1002/hbm.70627 [code]
Investigating the Contribution of Molecular-Enriched Functional Connectivity to Brain-Age Analysis.
Journal: Human brain mapping
In common: NumPy, humanconnectome.org/study/hcp-lifespan-aging, fMRI, 4 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.