Evidence map›Paper›PMID 36454982›Full record

ArticlePloS one2022

Automated landmarking via multiple templates.

Chi Zhang, Arthur Porto, Sara Rolfe, Altan Kocatulum, A Murat Maga

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Chi ZhangCenter for Development Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States of America.ORCID 0000-0002-0418-6354
Arthur PortoDepartment of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana, United States of America.
Sara RolfeCenter for Development Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States of America.
Altan KocatulumAlfred University, Alfred, New York, United States of America.
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

Inbred Mice Strains: Untapped Resource For Genome-Wide Quantitative Association Study For Craniofacial ShapeR03DE027110 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI MAGA, ALI MURAT · 2017 to 2018
$377k
NIDCR NIH HHS R03 DE027110
6 · The paper itself

Abstract

Manually collecting landmarks for quantifying complex morphological phenotypes can be laborious and subject to intra and interobserver errors. However, most automated landmarking methods for efficiency and consistency fall short of landmarking highly variable samples due to the bias introduced by the use of a single template. We introduce a fast and open source automated landmarking pipeline (MALPACA) that utilizes multiple templates for accommodating large-scale variations. We also introduce a K-means method of choosing the templates that can be used in conjunction with MALPACA, when no prior information for selecting templates is available. Our results confirm that MALPACA significantly outperforms single-template methods in landmarking both single and multi-species samples. K-means based template selection can also avoid choosing the worst set of templates when compared to random template selection. We further offer an example of post-hoc quality check for each individual template for further refinement. In summary, MALPACA is an efficient and reproducible method that can accommodate large morphological variability, such as those commonly found in evolutionary studies. To support the research community, we have developed open-source and user-friendly software tools for performing K-means multi-templates selection and MALPACA.

Indexed as

Biological EvolutionLabor, ObstetricFemaleHumansPhenotypePregnancySoftware

Identifiers

PMID36454982
PMCPMC9714854

What OpenQuestion 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 OpenQuestion graph.