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TitleReal-time cryo-electron microscopy data preprocessing with Warp.
Journal, issue, pagesNat Methods, Vol. 16, Issue 11, Page 1146-1152, Year 2019
Publish dateOct 7, 2019
AuthorsDimitry Tegunov / Patrick Cramer /
PubMed AbstractThe acquisition of cryo-electron microscopy (cryo-EM) data from biological specimens must be tightly coupled to data preprocessing to ensure the best data quality and microscope usage. Here we ...The acquisition of cryo-electron microscopy (cryo-EM) data from biological specimens must be tightly coupled to data preprocessing to ensure the best data quality and microscope usage. Here we describe Warp, a software that automates all preprocessing steps of cryo-EM data acquisition and enables real-time evaluation. Warp corrects micrographs for global and local motion, estimates the local defocus and monitors key parameters for each recorded micrograph or tomographic tilt series in real time. The software further includes deep-learning-based models for accurate particle picking and image denoising. The output from Warp can be fed into established programs for particle classification and 3D-map refinement. Our benchmarks show improvement in the nominal resolution, which went from 3.9 Å to 3.2 Å, of a published cryo-EM data set for influenza virus hemagglutinin. Warp is easy to install from http://github.com/cramerlab/warp and computationally inexpensive, and has an intuitive, streamlined user interface.
External linksNat Methods / PubMed:31591575 / PubMed Central
MethodsEM (single particle)
Resolution3.2 Å
Structure data

EMDB-0025:
Influenza hemagglutinin (HA) trimer reconstruction at 3.2 Angstrom resolution using data from EMPIAR-10097 processed with Warp and cryoSPARC
Method: EM (single particle) / Resolution: 3.2 Å

Source
  • Influenza A virus (A/Hong Kong/1/1968(H3N2))

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