Pith. sign in

REVIEW

Model compression for faster structural separation of macromolecules captured by Cellular Electron Cryo-Tomography

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 1801.10597 v1 pith:SGIYJM57 submitted 2018-01-31 q-bio.QM cs.CVstat.ML

Model compression for faster structural separation of macromolecules captured by Cellular Electron Cryo-Tomography

classification q-bio.QM cs.CVstat.ML
keywords classificationmacromoleculesmodelmodelsnetworksaccuracycapturedcompress
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
read the original abstract

Electron Cryo-Tomography (ECT) enables 3D visualization of macromolecule structure inside single cells. Macromolecule classification approaches based on convolutional neural networks (CNN) were developed to separate millions of macromolecules captured from ECT systematically. However, given the fast accumulation of ECT data, it will soon become necessary to use CNN models to efficiently and accurately separate substantially more macromolecules at the prediction stage, which requires additional computational costs. To speed up the prediction, we compress classification models into compact neural networks with little in accuracy for deployment. Specifically, we propose to perform model compression through knowledge distillation. Firstly, a complex teacher network is trained to generate soft labels with better classification feasibility followed by training of customized student networks with simple architectures using the soft label to compress model complexity. Our tests demonstrate that our compressed models significantly reduce the number of parameters and time cost while maintaining similar classification accuracy.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.