Discussion Summary for the 2012-13 Challenge Wah Chiu

Slides:



Advertisements
Similar presentations
Electron Optics Basic Introduction Bob Ashley
Advertisements

Lecture 11. Microscopy. Optical or light microscopy involves passing visible light transmitted through or reflected from the sample through a single or.
Microscope Lab Specimen Identification Specimen #1 (High Power)
Wah Chiu Basics in CryoEM Operations July 26, 2005.
Yifan Cheng Department of Biochemistry and Biophysics University of California San Francisco Electron Diffraction of 2D crystals - principle and data collection.
Electron Microscopy Chelsea Aitken Peter Aspinall
Ontology Classifications Acknowledgement Abstract Content from simulation systems is useful in defining domain ontologies. We describe a digital library.
Workshop on Biological Macromolecular Structure Models RCSB Protein Data Bank Rutgers, The State University of New Jersey.
Methods: Cryo-Electron Microscopy Biochemistry 4000 Dr. Ute Kothe.
The electron microscope: the contrast transfer function (CTF) Javier Vargas Centro Nacional de Biotecnología-CSIC
 Copyright © 2010 Pearson Education, Inc. Publishing as Prentice Hall Chapter 15 Implementing and Validating the Quality System.
Scipion: Toward software integration, reproducibility and validation in EM image processing Biocomputing Unit, Instruct Image Processing Center, CNB-CSIC.
Welcome to CMPE003 Personal Computer Concepts: Hardware and Software Winter 2003 UC Santa Cruz Instructor: Guy Cox.
Choosing Your Primary Research Method What do you need to find out that your literature did not provide?
Automation in Single-Particle Electron Microscopy
Scanning Electron Microscopy
Macromolecular Electron Microscopy Michael Stowell MCDB B231
Detecting Electrons: CCD vs Film Practical CryoEM Course July 26, 2005 Christopher Booth.
EMEN2 Steve Ludtke NCMI Baylor College of Medicine NCRR.
DDDs, Screening micrographs and CTF (Practical work) Vahid Abrishami.
LSBR Single particle processing workflow in Bsoft Bernard Heymann.
WORK TO BE DONE. Time line March-May 2013-Preparation June 2013-November Data collection December 2014-February Analysis and report preparation.
1 NumericNumeric Developing a statistical framework for measuring the digitisation of Europe’s cultural heritage  Numeric  Phillip Ramsdale The study.
Copyright © 2007 Pearson Education Canada 1 Chapter 14: Completing the Tests in the Sales and Collection Cycle: Accounts Receivable.
Instruct Image Processing Centre
Cryo-Electron Microscopy James Conway University of Pittsburgh School of Medicine 1. Making images image formation contrast function detectors – film &
Structural Study of the  12 Virus By:Elizabeth Brown.
Beam Induced Movement and DDDs Javier Vargas Centro Nacional de Biotecnología-CSIC
Workshop Structural Proteomics of Biological Complexes.
Reaching the Information Limit in Cryo- EM of Biological Macromolecules: Experimental Aspects -Robert M. Glaeser and Richard J. Hall (2011)
Copyright © 2011 by The McGraw-Hill Companies, Inc. All rights reserved. McGraw-Hill/Irwin Using Specialized Research Designs.
TED Talk21: Creating a dynamic and joyful environment Marie Alcock and Allison Zmuda.
Observation of latent image specks in nuclear emulsion for the purpose of precise estimation of local deposit energy Kimio Niwa* Toshiyuki Toshito** Ken'ichi.
Wah Chiu Basics in CryoEM Operations June 8, 2007
Modulation Transfer Function (MTF)
MARCH 1 Project Management Problem statement l no hurdles, no problem just a goal l open-ended … no single correct answer l closed-ended … single answer.
Slide 1 Eurostat Unit B3 – Statistical Information Technology XBRL pilot Task Force 27 September 2006 Status of XDIS/XBRL pilot project Giuseppe Sindoni.
HERA Second European Stakeholder Workshop July Human & Environmental Risk Assessment An A.I.S.E and CEFIC initiative on targeted risk assessment.
Summer '07 at CLS Small Angle X-Ray Scattering Peter ChenChithra Karunakaran & Konstantine Kaznatcheev.
Hierarchy of Biological Complexity Interactions of machines (molecular and cellular dynamics) Macromolecular machines Proteins and nucleic acids Sequences.
Chapter 10: Project Communications Management Information Technology Project Management, Fifth Edition.
Abstract A step-wise or ‘tiered’ approach has been used as a rational procedure to conduct environmental risk assessments in many disciplines. The Technical.
SEMINAR ON PRESENTED BY BRAHMABHATT BANSARI K. M. PHARM PART DEPARTMENT OF PHARMACEUTICS AND PHARMACEUTICAL TECHNOLGY L. M. COLLEGE OF PHARMACY.
Date of download: 6/27/2016 Copyright © 2016 SPIE. All rights reserved. Experimental configuration. (a), Setup. LD, laser diode; BS, beam splitter; F,
REPORT TO EWG MEMBER (CORRESPONDENCE) Plan of Actions for (May) (June) (July) (August) (September)
Page 1 Cryo-EM Services by Creative Biostructure.
JRA3 Introduction Åke Edlund EGEE Security Head
What is cryo EM? EM = (Transmission) Electron Microscopy
Cryo-em Electron microscopy (EM) has become an extremely popular method for the ultrastructural study of macromolecules, cells and tissues. With our in-house.
Electron microscope Electron microscopy (EM) has become an extremely popular method for the ultrastructural study of macromolecules, cells and tissues.
Cryo-em services Electron microscopy (EM) has become an extremely popular method for the ultrastructural study of macromolecules, cells and tissues. With.
Chapter 3 The Marketing Research Process and
Cryo-EM Services Cryo-EM Services in Creative Biostructure.
Volume 14, Issue 11, Pages (November 2006)
Volume 23, Issue 9, Pages (September 2015)
PAIN OUT network in Mexico
Hans Elmlund, Dominika Elmlund, Samy Bengio  Structure 
Volume 18, Issue 8, Pages (August 2010)
Structure of the Oligosaccharyl Transferase Complex at 12 Å Resolution
Volume 20, Issue 12, Pages (December 2012)
The 2015 CryoEM Map and Model Validation Challenges
Volume 19, Issue 4, Pages (April 2011)
Single-Particle Cryo-EM at Crystallographic Resolution
Volume 18, Issue 1, Pages (January 2010)
Zheng Liu, Fei Guo, Feng Wang, Tian-Cheng Li, Wen Jiang  Structure 
A Physics Analysis of a Particle Flow Algorithm
Erika J Mancini, Felix de Haas, Stephen D Fuller  Structure 
Validation of Cryo-EM Structure of IP3R1 Channel
Volume 6, Issue 4, Pages (April 1998)
Presentation transcript:

Discussion Summary for the Challenge Wah Chiu

Past Challenges Particle Picking Reconstruction Software Modeling Challenge

Suggested Challenges for Cryo-EM CTF estimate (determination) 11 Assess quality of micrographs 10 Reconstruction refinement (Quality of the map) 9 Particle picking 9 2-D Image classification 1 3-D classification 5 Meta challenge (e.g. CTF) 0 Different teams work on different steps 0 Modeling experimental data 5 Generate experimental and theoretical phantom 0 Biochemical homogeneity 0 Cryo-specimen preparation 3 Challenge in obtaining the best data set 1 Establish intersection points among different softwares 0 Test with published structures (e.g. ATP complex) 0

Practical Consideration for Challenge Events Resources available in the community Interesting, challenging and feasible Eliminate ego (nameless) Cash for the winners (Euro or $) from the EM companies Publications in respectable journals Of interest to the community in general

Choice of a Challenge for CTF estimate (determination) 11 Assess quality of micrographs 10 Reconstruction refinement (Quality of the map) 9 Particle picking 9

Establish a Data Set of ~100 micrographs with different experimental conditions Defocus range: 0.5, 1.0, , 3, 5 micron 200 and 300 kV microscope “Small” Astigmatism and drift Variation of defocus within a micrograph due to various reasons Recording medium: film, CCD, Direct detector With and without Carbon or graphene film Size of particles MDa Particle concentration (>50 particles/frame) without C film Electron dose 20 e/ Å 2 per image different defocus Magnification is chosen to have Sampling: Å/pixel Ice thickness (typical for the experiment) Cumulative Envelope function

Define the FOM Determine the defocus U and defocus V and the angle as defined for data interchange Two photographs with different defocuses in well-calibrated microscopes to validate the true defocus values in all cases

Specimen choices 60S Ribosome (1.6 MDa), 300 kV, CCD, C film: J Frank GroEL (800kDa) 200 kV, CCD, DDD, no C film: A Cheng Lipid nanodisk (1MDa), 300 & 200 kV, CCD and CMOS, C and graphene: Henning Apoferritin (500 kDa) 200 kV, film, no carbon: Richard Henderson

Phases of Task in preparing the Data Monthly conference call initiated by J-M Carazo among the experimentalists. (March, April, May) to share progress and hurdles Focal pair Data generation and analysis by the suppliers of each of the 4 specimens – June 1, 2012 Use the J-M Carazo infrastructure to share data Meet at the Gordon conference to assess the collected images and to decide the policy for the competition among the community

Road Map of Challenges in the Future Suggested meeting in US in the winter of 2013 Financed by HHMI, NIH or NSF