Evidence map›Paper›PMID 38826373›Full record

ArticlebioRxiv : the preprint server for biology2024

Leveraging Descriptor Learning and Functional Map-based Shape Matching for Automatic Landmark Acquisition.

Oshane O Thomas, A Murat Maga

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

2 authors.

Oshane O ThomasCenter for Development Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States of America.ORCID 0000-0003-3500-5445
A Murat MagaCenter for Development Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States of America.ORCID 0000-0002-7921-9018

Funding

Utilization of Advanced Technologies for the Understanding of Human Structural Birth DefectsP01HD104435 · NICHD · SEATTLE CHILDREN'S HOSPITAL · PI MAGA, ALI MURAT · 2021 to 2025
$8.4M
Maternal alcohol exposure: impact on genetic control of craniofacial phenotypeR00DE021417 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI MAGA, ALI MURAT · 2013 to 2015
$737k
Maternal alcohol exposure: impact on genetic control of craniofacial phenotypeK99DE021417 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI MAGA, ALI MURAT · 2011 to 2012
$251k
NICHD NIH HHS P01 HD104435NIDCR NIH HHS K99 DE021417NIDCR NIH HHS R00 DE021417
6 · The paper itself

Abstract

Geometric morphometrics is widely employed across the biological sciences for the quantification of morphological traits. However, the scalability of these methods to large datasets is hampered by the requisite placement of landmarks, which can be laborious and time consuming if done manually. Additionally, the selected landmarks embody a particular hypothesis regarding the critical geometry pertinent to the biological inquiry at hand. Modifying this hypothesis lacks flexibility, necessitating the acquisition of an entirely new set of landmarks on the entire dataset to reflect any theoretical adjustments. In our research, we investigate the precision and accuracy of landmarks derived from the comprehensive set of functional correspondences acquired through the functional map framework of geometry processing. We use a deep functional map network to learn shape descriptors that effectively yield functional map-based and point-to-point correspondences between the specimens in our dataset. We then interrogate these maps to identify corresponding landmarks given manually placed landmarks from the entire dataset. We assess our method by automating the landmarking process on a dataset comprising mandibles from various rodent species, comparing its efficacy against MALPACA, a cutting-edge technique for automatic landmark placement. Compared to MALPACA, our model is notably faster and maintains competitive accuracy. The Root Mean Square Error (RMSE) analysis reveals that while MALPACA generally exhibits the lowest RMSE, our models perform comparably, especially with smaller training datasets, suggesting strong generalizability. Visual evaluations confirm the precision of our landmark placements, with deviations remaining within an acceptable range. These findings underscore the potential of unsupervised learning models in anatomical landmark placement, providing a viable and efficient alternative to traditional methods.

Identifiers

PMID38826373
PMCPMC11142217

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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 OpenQuestion graph.