Non-uniform refinement: adaptive regularization improves single-particle cryo-EM reconstruction.
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[1] D. Rubin,et al. Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper , 1977 .
[2] G. Wahba. A Comparison of GCV and GML for Choosing the Smoothing Parameter in the Generalized Spline Smoothing Problem , 1985 .
[3] M. Heel,et al. Exact filters for general geometry three dimensional reconstruction , 1986 .
[4] Petros Maragos,et al. A comparison of the energy operator and the Hilbert transform approach to signal and speech demodulation , 1994, Signal Process..
[5] Michael Felsberg,et al. The monogenic signal , 2001, IEEE Trans. Signal Process..
[6] R. Henderson,et al. Optimal determination of particle orientation, absolute hand, and contrast loss in single-particle electron cryomicroscopy. , 2003, Journal of molecular biology.
[7] John P. Overington,et al. How many drug targets are there? , 2006, Nature Reviews Drug Discovery.
[8] Gene H. Golub,et al. Generalized cross-validation as a method for choosing a good ridge parameter , 1979, Milestones in Matrix Computation.
[9] Nikolaus Grigorieff,et al. FREALIGN: high-resolution refinement of single particle structures. , 2007, Journal of structural biology.
[10] Yoel Shkolnisky,et al. Fast wavelet-based single-particle reconstruction in Cryo-EM , 2011, 2011 IEEE International Symposium on Biomedical Imaging: From Nano to Macro.
[11] Sjors H.W. Scheres,et al. A Bayesian View on Cryo-EM Structure Determination , 2012, 2012 9th IEEE International Symposium on Biomedical Imaging (ISBI).
[12] Sjors H.W. Scheres,et al. RELION: Implementation of a Bayesian approach to cryo-EM structure determination , 2012, Journal of structural biology.
[13] Alp Kucukelbir,et al. A Bayesian adaptive basis algorithm for single particle reconstruction. , 2012, Journal of structural biology.
[14] Shaoxia Chen,et al. Prevention of overfitting in cryo-EM structure determination , 2012, Nature Methods.
[15] R. Henderson,et al. High-resolution noise substitution to measure overfitting and validate resolution in 3D structure determination by single particle electron cryomicroscopy☆ , 2013, Ultramicroscopy.
[16] A. Steven,et al. One number does not fit all: mapping local variations in resolution in cryo-EM reconstructions. , 2013, Journal of structural biology.
[17] Hemant D. Tagare,et al. The Local Resolution of Cryo-EM Density Maps , 2013, Nature Methods.
[18] Michael S. Spilman,et al. ResLog plots as an empirical metric of the quality of cryo-EM reconstructions. , 2014, Journal of structural biology.
[19] D. Julius,et al. Structure of the TRPA1 ion channel suggests regulatory mechanisms , 2015, Nature.
[20] Yifan Cheng. Single-Particle Cryo-EM at Crystallographic Resolution , 2015, Cell.
[21] Muyuan Chen,et al. High resolution single particle refinement in EMAN2.1. , 2016, Methods.
[22] David J Weber,et al. Structure of the STRA6 receptor for retinol uptake , 2016, Science.
[23] David J. Fleet,et al. cryoSPARC: algorithms for rapid unsupervised cryo-EM structure determination , 2017, Nature Methods.
[24] Jaakko Lehtinen,et al. Noise2Noise: Learning Image Restoration without Clean Data , 2018, ICML.
[25] Erik Lindahl,et al. New tools for automated high-resolution cryo-EM structure determination in RELION-3 , 2018, eLife.
[26] Claudio Ciferri,et al. Cryo-EM in drug discovery: achievements, limitations and prospects , 2018, Nature Reviews Drug Discovery.
[27] Alexis Rohou,et al. cisTEM: User-friendly software for single-particle image processing , 2017, bioRxiv.
[28] B. Carragher,et al. Cryo-EM for Small Molecules Discovery, Design, Understanding, and Application. , 2018, Cell chemical biology.
[29] José María Carazo,et al. MonoRes: Automatic and Accurate Estimation of Local Resolution for Electron Microscopy Maps. , 2018, Structure.
[30] Yifan Cheng. Membrane protein structural biology in the era of single particle cryo-EM. , 2018, Current opinion in structural biology.
[31] Kailash Ramlaul,et al. A Local Agreement Filtering Algorithm for Transmission EM Reconstructions , 2019, Journal of structural biology.
[32] Alexis Rohou,et al. Structural Basis of Nav1.7 Inhibition by a Gating-Modifier Spider Toxin , 2019, Cell.
[33] D. Sabatini,et al. Structural basis for the docking of mTORC1 on the lysosomal surface , 2019, Science.
[34] Yong Zi Tan,et al. Structure of an endosomal signaling GPCR–G protein–β-arrestin megacomplex , 2019, Nature Structural & Molecular Biology.
[35] Tristan Bepler,et al. Topaz-Denoise: general deep denoising models for cryoEM and cryoET , 2019, Nature Communications.
[36] G. Hummer,et al. Conformation space of a heterodimeric ABC exporter under turnover conditions , 2019, Nature.
[37] Dimitry Tegunov,et al. Real-time cryo–EM data pre-processing with Warp , 2019, Nature Methods.
[38] J. McLellan,et al. Structure of the Respiratory Syncytial Virus Polymerase Complex , 2019, Cell.
[39] Yong Zi Tan,et al. Structure and Drug Resistance of the Plasmodium falciparum Transporter PfCRT , 2019, Nature.
[40] Takanori Nakane,et al. Mitigating local over-fitting during single particle reconstruction with SIDESPLITTER , 2020, Journal of structural biology.
[41] B. Graham,et al. Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation , 2020, Science.
[42] Tristan Bepler,et al. Topaz-Denoise: general deep denoising models for cryoEM and cryoET , 2020, Nature communications.