Evidence map›Paper›PMID 29951483›Full record

ArticleFrontiers in molecular biosciences2018

Benchmarking cryo-EM Single Particle Analysis Workflow.

Laura Y Kim, William J Rice, Edward T Eng, Mykhailo Kopylov, Anchi Cheng, Ashleigh M Raczkowski, Kelsey D Jordan, Daija Bobe, Clinton S Potter, Bridget Carragher

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Multi-species cryoEM calibration and workflow verification standard.Acta crystallographica. Section F, Structural biology communications · 2024
    Article
  7. Multi-species cryoEM calibration and workflow verification standard.bioRxiv : the preprint server for biology · 2024
    Article
  8. VitroJet: new features and case studies.Acta crystallographica. Section D, Structural biology · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Tools for Decoding Ubiquitin Signaling in DNA Repair.Frontiers in cell and developmental biology · 2021
    Review
  18. Progress Towards CryoEM: Negative-Stain Procedures for Biological Samples.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  19. Leginon: New features and applications.Protein science : a publication of the Protein Society · 2021
    Article
  20. 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

10 authors.

Laura Y KimSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
William J RiceSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Edward T EngSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Mykhailo KopylovSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Anchi ChengSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Ashleigh M RaczkowskiSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Kelsey D JordanSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Daija BobeSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Clinton S PotterSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.
Bridget CarragherSimons Electron Microscopy Center, New York Structural Biology Center, New York, NY, United States.

Funding

TRD #3: An automated and streamlined pipeline for in-situ molecular microscopyP41GM103310 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI DE MARCO, ALEX, KIEFT, JEFFREY S · 2012 to 2021
$14.7M
NIGMS NIH HHS P41 GM103310
6 · The paper itself

Abstract

Cryo electron microscopy facilities running multiple instruments and serving users with varying skill levels need a robust and reliable method for benchmarking both the hardware and software components of their single particle analysis workflow. The workflow is complex, with many bottlenecks existing at the specimen preparation, data collection and image analysis steps; the samples and grid preparation can be of unpredictable quality, there are many different protocols for microscope and camera settings, and there is a myriad of software programs for analysis that can depend on dozens of settings chosen by the user. For this reason, we believe it is important to benchmark the entire workflow, using a standard sample and standard operating procedures, on a regular basis. This provides confidence that all aspects of the pipeline are capable of producing maps to high resolution. Here we describe benchmarking procedures using a test sample, rabbit muscle aldolase.

Indexed as

alignmentbenchmarkingcryo-electron microscopyresolutionsingle particle workflowstructural biology

Identifiers

PMID29951483
PMCPMC6009202

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.