Evidence map›Paper›PMID 32294468›Full record

ArticleStructure (London, England : 1993)2020

High-Throughput Cryo-EM Enabled by User-Free Preprocessing Routines.

Yilai Li, Jennifer N Cash, John J G Tesmer, Michael A Cianfrocco

Abstract read
In one paragraph

Article in Structure (London, England : 1993), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. CryoSift: an accessible and automated CNN-driven tool for cryo-EM 2D class selection.Acta crystallographica. Section F, Structural biology communications · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Rapid structural analysis of bacterial ribosomesbioRxiv : the preprint server for biology · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Mass spectrometers as cryoEM grid preparation instruments.Current opinion in structural biology · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Evolving Experimental Techniques for Structure-Based Drug Design.The journal of physical chemistry. B · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Yilai LiLife Sciences Institute, Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA.
Jennifer N CashLife Sciences Institute, Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA.
John J G TesmerDepartments of Biological Sciences and of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN, USA.
Michael A CianfroccoLife Sciences Institute, Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA. Electronic address: mcianfro@umich.edu.

Funding

Structure, function, and inhibition of G protein-coupled receptor kinasesR01HL071818 · NHLBI · UNIVERSITY OF TEXAS AUSTIN · PI TESMER, JOHN · 2004 to 2023
$7.1M
Structure and Function of the LPLA2/LCAT Acyltransferase FamilyR01HL122416 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TESMER, JOHN · 2015 to 2018
$1.9M
GPCR - Linked RhoGEFs in Tumor Growth and MetastasisR01CA221289 · NCI · PURDUE UNIVERSITY · PI TESMER, JOHN · 2018 to 2022
$1.9M
Silicon Mechanics Compute ClusterS10OD020011 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SKINIOTIS, GEORGIOS · 2015 to 2015
$490k
NCI NIH HHS R01 CA221289NHLBI NIH HHS R01 HL071818NHLBI NIH HHS R01 HL122416NIH HHS S10 OD020011
6 · The paper itself

Abstract

Single-particle cryoelectron microscopy (cryo-EM) continues to grow into a mainstream structural biology technique. Recent developments in data collection strategies alongside new sample preparation devices herald a future where users will collect multiple datasets per microscope session. To make cryo-EM data processing more automatic and user-friendly, we have developed an automatic pipeline for cryo-EM data preprocessing and assessment using a combination of deep-learning and image-analysis tools. We have verified the performance of this pipeline on a number of datasets and extended its scope to include sample screening by the user-free assessment of the qualities of a series of datasets under different conditions. We propose that our workflow provides a decision-free solution for cryo-EM, making data preprocessing more generalized and robust in the high-throughput era as well as more convenient for users from a range of backgrounds.

Indexed as

Cryoelectron MicroscopyDeep LearningHigh-Throughput Screening AssaysImage Processing, Computer-AssistedProtein Conformationautomaticcryo-EMdeep learning;pipeline

Identifiers

PMID32294468
PMCPMC7347462

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Registered trials

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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.