Evidence map›Paper›PMID 35362465›Full record

ArticleActa crystallographica. Section D, Structural biology2022

On bias, variance, overfitting, gold standard and consensus in single-particle analysis by cryo-electron microscopy.

C O S Sorzano, A Jiménez-Moreno, D Maluenda, M Martínez, E Ramírez-Aportela, J Krieger, R Melero, A Cuervo, J Conesa, J Filipovic and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Acta crystallographica. Section D, Structural biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
6.3field-weighted citation impact, top 4% of its field
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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. How many (distinguishable) classes can we identify in single-particle analysis?Acta crystallographica. Section D, Structural biology · 2025
    Article
  6. Amortized template matching of molecular conformations from cryoelectron microscopy images using simulation-based inference.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
  9. Molecular regulation of calcium-sensing receptor (CaSR)-mediated signaling.Chronic diseases and translational medicine · 2024
    Review
  10. Factors affecting macromolecule orientations in thin films formed in cryo-EM.Acta crystallographica. Section D, Structural biology · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
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

23 authors at 4 institutions in 3 countries.

C O S SorzanoBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
A Jiménez-MorenoBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
D MaluendaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
M MartínezBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
E Ramírez-AportelaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
J KriegerBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
R MeleroBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
A CuervoBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
J ConesaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
J FilipovicMasaryk University, Brno, Czech Republic.
P ConesaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
L Del CañoBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
Y C FonsecaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
J Jiménez-de la MorenaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
P LosanaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
R Sánchez-GarcíaBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
D StrelakBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
E Fernández-GiménezBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
F P de Isidro-GómezBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
D HerrerosBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
J L VilasSchool of Engineering and Applied Science, Yale University, New Haven, CT 06520-829, USA.
R MarabiniEscuela Politecnica Superior, Universidad Autónoma de Madrid, 28049 Cantoblanco, Madrid, Spain.
J M CarazoBiocomputing Unit, Centro Nacional de Biotecnologia (CNB-CSIC), Calle Darwin 3, 28049 Cantoblanco, Madrid, Spain.
Centro Nacional de Biotecnología · ESMasaryk University · CZUniversidad Autónoma de Madrid · ESYale University · US

Funding

Comunidad de Madrid S2017/BMD-3817Horizon 2020 Framework Programme, H2020 Excellent Science 654248Horizon 2020 Framework Programme, H2020 Excellent Science 731005Horizon 2020 Framework Programme, H2020 Excellent Science 810057Horizon 2020 Framework Programme, H2020 Excellent Science 824087Horizon 2020 Framework Programme, H2020 Excellent Science 857203Horizon 2020 Framework Programme, H2020 Excellent Science 871037Horizon 2020 Framework Programme, H2020 Excellent Science CZ.02.1.01/0.0/0.0/16_013/0001802Instituto de Salud Carlos III PT17/0009/0010"la Caixa" Foundation LCF/BQ/DI18/11660021Ministerio de Ciencia, Innovación y Universidades PID2019-104757RB-I00Ministerio de Ciencia, Innovación y Universidades SEV 2017-0712
6 · The paper itself

Abstract

Cryo-electron microscopy (cryoEM) has become a well established technique to elucidate the 3D structures of biological macromolecules. Projection images from thousands of macromolecules that are assumed to be structurally identical are combined into a single 3D map representing the Coulomb potential of the macromolecule under study. This article discusses possible caveats along the image-processing path and how to avoid them to obtain a reliable 3D structure. Some of these problems are very well known in the community. These may be referred to as sample-related (such as specimen denaturation at interfaces or non-uniform projection geometry leading to underrepresented projection directions). The rest are related to the algorithms used. While some have been discussed in depth in the literature, such as the use of an incorrect initial volume, others have received much less attention. However, they are fundamental in any data-analysis approach. Chiefly among them, instabilities in estimating many of the key parameters that are required for a correct 3D reconstruction that occur all along the processing workflow are referred to, which may significantly affect the reliability of the whole process. In the field, the term overfitting has been coined to refer to some particular kinds of artifacts. It is argued that overfitting is a statistical bias in key parameter-estimation steps in the 3D reconstruction process, including intrinsic algorithmic bias. It is also shown that common tools (Fourier shell correlation) and strategies (gold standard) that are normally used to detect or prevent overfitting do not fully protect against it. Alternatively, it is proposed that detecting the bias that leads to overfitting is much easier when addressed at the level of parameter estimation, rather than detecting it once the particle images have been combined into a 3D map. Comparing the results from multiple algorithms (or at least, independent executions of the same algorithm) can detect parameter bias. These multiple executions could then be averaged to give a lower variance estimate of the underlying parameters.

Indexed as

Imaging, Three-DimensionalBiasConsensusCryoelectron MicroscopyReproducibility of Resultsbiascryo-electron microscopygold standardimage processingoverfittingparameter estimationsingle-particle analysisvariance

Identifiers

PMID35362465
PMCPMC8972802
OpenAlexW4220747914

What OpenQuestion holds

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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.