Evidence map›Paper›PMID 39185219›Full record

ArticlebioRxiv : the preprint server for biology2024

qPRF: A system to accelerate population receptive field decoding.

Sebastian Waz, Yalin Wang, Zhong-Lin Lu

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Sebastian WazCenter for Neural Science, New York University, 4 Washington Place, New York, 10003, NY, USA.
Yalin WangSchool of Computing and Augmented Intelligence, Arizona State University, 699 S. Mill Avenue, Tempe, 85281, AZ, USA.ORCID 0000-0002-6241-735X
Zhong-Lin LuDivision of Arts and Sciences, NYU Shanghai, 567 West Yangsi Road, Pudong New District, 200124, Shanghai, China.ORCID 0000-0002-7295-727X

Funding

Hierarchical Bayesian Analysis of Retinotopic Maps of the Human Visual Cortex with Conformal GeometryR01EY032125 · NEI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI LU, ZHONG-LIN, WANG, YALIN · 2021 to 2024
$1.2M
NEI NIH HHS R01 EY032125
6 · The paper itself

Abstract

Patterns of BOLD response can be decoded using the population receptive field (PRF) model to reveal how visual input is represented on the cortex (Dumoulin and Wandell, 2008). The time cost of evaluating the PRF model is high, often requiring days to decode BOLD signals for a small cohort of subjects. We introduce the qPRF, an efficient method for decoding that reduced the computation time by a factor of 1436 when compared to another widely available PRF decoder (Kay, Winawer, Mezer and Wandell, 2013) on a benchmark of data from the Human Connectome Project (HCP; Van Essen, Smith, Barch, Behrens, Yacoub and Ugurbil, 2013). With a specially designed data structure and an efficient search algorithm, the qPRF optimizes the five PRF model parameters according to a least-squares criterion. To verify the accuracy of the qPRF solutions, we compared them to those provided by Benson, Jamison, Arcaro, Vu, Glasser, Coalson, Van Essen, Yacoub, Ugurbil, Winawer and Kay (2018). Both hemispheres of the 181 subjects in the HCP data set (a total of 10,753,572 vertices, each with a unique BOLD time series of 1800 frames) were decoded by qPRF in 15.2 hours on an ordinary CPU. The absolute difference in

Indexed as

Data structuresOptimizationPopulation receptive field modelRetinotopic mappingVision

Identifiers

PMID39185219
PMCPMC11343136

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.