Evidence map›Paper›PMID 39541350›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

BIFROST: A method for registering diverse imaging datasets of the

Bella E Brezovec, Andrew B Berger, Yukun A Hao, Albert Lin, Osama M Ahmed, Diego A Pacheco, Stephan Y Thiberge, Mala Murthy, Thomas R Clandinin

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. BIFROST: A method for registering diverse imaging datasets of theProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Bella E Brezovec *Department of Neurobiology, Stanford University, Stanford, CA 94305.
Andrew B Berger *Department of Neurobiology, Stanford University, Stanford, CA 94305.
Yukun A Hao *Department of Neurobiology, Stanford University, Stanford, CA 94305.
Albert Lin *Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08544.ORCID 0000-0002-4541-5889
Osama M Ahmed *Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08544.ORCID 0000-0003-3539-3150
Diego A PachecoPrinceton Neuroscience Institute, Princeton University, Princeton, NJ 08544.ORCID 0000-0003-1638-2376
Stephan Y ThibergePrinceton Neuroscience Institute, Princeton University, Princeton, NJ 08544.ORCID 0000-0002-6583-6613
Mala MurthyPrinceton Neuroscience Institute, Princeton University, Princeton, NJ 08544.
Thomas R ClandininDepartment of Neurobiology, Stanford University, Stanford, CA 94305.

Funding

Population Neural Activity Mediating Sensory Perception Across ModalitiesR01NS110060 · NINDS · STANFORD UNIVERSITY · PI CLANDININ, THOMAS ROBERT, GANGULI, SURYA · 2018 to 2022
$5.4M
Uncovering the Neural Mechanisms that Flexibly Link Sensory Processing to BehaviorR35NS111580 · NINDS · PRINCETON UNIVERSITY · PI Mala Murthy · 2019 to 2026
$5.0M
Dissecting Neural Circuit Computations in the Peripheral Visual SystemR01EY022638 · NEI · STANFORD UNIVERSITY · PI CLANDININ, THOMAS ROBERT · 2012 to 2021
$3.5M
BRAINS Fellowship NABurroughs Wellcome Fund (BWF) NAChan-Zuckerberg BioHub NAHHS | NIH | BRAIN Initiative (The BRAIN Initiative) NS110060HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01EY022638HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R35NEI NIH HHS R01 EY022638NINDS NIH HHS R01 NS110060NINDS NIH HHS R35 NS111580NSF | National Science Foundation Graduate Research Fellowship Program (GRFP) NAPrinceton Presidential Postdoctoral Fellowship NASimons Collaboration NASimons Collaboration on the Global Brain Bridge to Independence Award NA
6 · The paper itself

Abstract

Imaging methods that span both functional measures in living tissue and anatomical measures in fixed tissue have played critical roles in advancing our understanding of the brain. However, making direct comparisons between different imaging modalities, particularly spanning living and fixed tissue, has remained challenging. For example, comparing brain-wide neural dynamics across experiments and aligning such data to anatomical resources, such as gene expression patterns or connectomes, requires precise alignment to a common set of anatomical coordinates. However, reaching this goal is difficult because registering in vivo functional imaging data to ex vivo reference atlases requires accommodating differences in imaging modality, microscope specification, and sample preparation. We overcome these challenges in

Indexed as

BrainAnimalsConnectomeDrosophilaDrosophila melanogasterImage Processing, Computer-AssistedalignmentconnectomeDrosophilaregistration

Identifiers

PMID39541350
PMCPMC11588091

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.