CryoSift: an accessible and automated CNN-driven tool for cryo-EM 2D class selection
Автор: International Union of Crystallography
Загружено: 2025-12-11
Просмотров: 133
Описание:
Video interview with the authors.
Published in Acta Cryst. F
https://doi.org/10.1107/S2053230X2500...
CryoSift: an accessible and automated CNN-driven tool for cryo-EM 2D class selection
Single-particle cryo-electron microscopy (cryo-EM) has become an essential tool in structural biology. However, automating repetitive tasks remains an ongoing challenge in cryo-EM data-set processing. Here, we present a platform-independent convolutional neural network (CNN) tool for assessing the quality of 2D averages to enable the automatic selection of suitable particles for high-resolution reconstructions, termed CryoSift. We integrate CryoSift into a fully automated processing pipeline using the existing cryosparc-tools library. Our integrated and customizable 2D assessment workflow enables high-throughput processing that accommodates experienced to novice cryo-EM users.
00:00 Main editor intro:
01:00 Stephen Muench intro
01:10 Jan Hannes-Schäfer intro
01:30 Scott M. Stagg intro
01:45 Michael A. Cianfrocco
01:58 What specific gap in cryo-EM workflows were you seeking to plug with CryoSift?
03:00 How does CryoSift combine image features with metadata to improve class quality prediction?
04:30 When training the CNN, what training data were used and how did you ensure diversity across the samples?
06:04 Why do you recommend a cut-off of 3.5 and what is the trade-off?
07:34 How does CryoSift integrate into the different platforms, such as CryoSPARC or Relion?
08:49 Which evaluation metrics were use to evaluate reconstruction quality and why were they chosen?
10:55 How much does CryoSift help reduce subjectivity between practitioners?
12:10 What major limitations would you highlight for future improvement?
13:30 Given the rapid improvement in CryoEM and machine learning, how automated do you think the process is going to become?
15:00 How did the tool and the paper come together?
16:20 MX is know for large software suites such as CCP4 or PHENIX; will CryoSift be a step in that direction for CryoEM?
18:30 Unexpected features in data or metadata might be wrong, or right and interesting. How might the software prevent the suppression of interesting features?
20:33 What drove you to develop CryoSift?
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