Neuroinformatics: Sharing, Organizing and Accessing Data and Models

Total Page:16

File Type:pdf, Size:1020Kb

Neuroinformatics: Sharing, Organizing and Accessing Data and Models Neuroinformatics: sharing, organizing and accessing data and models Arnd Roth Wolfson Institute for Biomedical Research University College London The optogenetics revolution Fuhrmann et al., 2015 The optogenetics revolution Fuhrmann et al., 2015 The connectomics revolution Helmstaedter et al., 2013 The connectomics revolution Helmstaedter et al., 2013 Connectomics data mining Jonas & Körding, 2015 Connectomics data mining Jonas & Körding, 2015 Deep artificial neural networks Mnih et al., 2015 Neuroinformatics: sharing, organizing and accessing experimental data Allen Institute http://alleninstitute.org Janelia Research Campus https://www.janelia.org/ Open Connectome Project http://www.openconnectomeproject.org/ Cell Image Library http://www.cellimagelibrary.org/ Human Brain Project http://www.humanbrainproject.eu/ INCF http://www.incf.org/ Single neuron and network simulators NEURON http://www.neuron.yale.edu/neuron/ GENESIS https://www.genesis-sim.org/ MOOSE http://moose.ncbs.res.in/ PSICS http://www.psics.org/ NEST http://www.nest-initiative.org/ Meta-simulators: simulator- independent model description PyNN http://neuralensemble.org/PyNN/ neuroConstruct http://www.neuroconstruct.org/ NeuroML http://www.neuroml.org/ NineML http://software.incf.org/software/nineml neuroConstruct http://www.opensourcebrain.org 12 neuroConstruct Software tool (written in Java) developed in Angus Silver’s Laboratory of Synaptic Transmission and Information Processing Facilitates development of 3D network models of biologically realistic cells through graphical interface Allows anatomical positioning of cells and complex connectivity of axons/dendrites Automatically generates scripts for running simulations in NEURON/GENESIS/MOOSE/PSICS/PyNN & more Support for import, export & conversion of NeuroML http://www.opensourcebrain.org 13 neuroConstruct – latest developments neuroConstruct can generate code for Parallel NEURON - Most widespread platform for large scale detailed neuronal simulations - Near linear speedup of simulations up to hundreds of cores Python scripting interface - Python becoming language of choice for neuroinformatics applications - Gives access to all functionality “behind the GUI” Open Source Brain - Platform for sharing & collaboratively developing models in computational neuroscience - Many neuroConstruct projects from multiple brain regions available http://www.opensourcebrain.org 14 Example using Python interface & Parallel NEURON 3D version of Traub et al 2005 Thalamocortical column model Parallel simulation durations scale approx. linearly up to 200 processors & 10,000 cells Wider interoperability framework http://www.opensourcebrain.org 16 Towards multiscale simulation: from molecules to circuits MCell http://www.mcell.org/ CellBlender http://www.mcell.org/ STEPS http://steps.sourceforge.net/ TrakEM2 http://fiji.sc/TrakEM2 TREES toolbox http://www.treestoolbox.org/ Public databases of neural models ModelDB https://senselab.med.yale.edu/ModelDB/ NeuroMorpho.org http://neuromorpho.org/ BigNeuron http://alleninstitute.org/bigneuron OpenSourceBrain http://www.opensourcebrain.org/ Human Brain Project http://www.humanbrainproject.eu/ How to make computational neuroscience a more accepted scientific approach? Reproducibility: easy to rerun and validate simulation result reported in a scientific paper. Accessibility: available to theoretical and experimental neuroscientists in an understandable format Portability: cross-simulator validation and exchange of models and components enabling reuse Transparency: exposure of internal properties and automated validation http://www.opensourcebrain.org 19 Neuroinformatics infrastructure NeuroML A simulator-independent language for describing and exchanging detailed neuronal and network models LEMS Compact and flexible model description language that underlies NeuroML 2 The Open Source Brain Initiative Accessible repository of standardized models and infrastructure for collaborative, open source model development http://www.opensourcebrain.org 20 The Open Source Brain repository 21 Current model development life-cycle 22 Current model development life-cycle http://www.opensourcebrain.org 23 OSB collaborative development scenario http://www.opensourcebrain.org 24 OSB iterative development through critical evaluation Experiment Model Validate http://www.opensourcebrain.org 26 A Whole Community Approach • Must bring experimental and theoretical & computational neuroscience closer. • While the latter seek minimal models, the former want hard earned experimental facts not to be ignored. • As the functional principles of neuronal networks in the brain remain elusive, and the interactions are often highly non-linear, ignoring biological facts without thought to errors can easily result in misleading conclusions, and erroneous theories of brain function. • Adhoc simplification is a matter of taste Level of detail: A rift in neuroscience 1. Simplify the details – minimal model for hypothesis-driven science – Adhoc simplification – Minimal for which question? vs 2. Consider all known – data-driven is data-ready – Hypothesis-free integration of facts – Algorithms fill in gaps from sparse data – Fewer free parameters! – Avoid wasting time hand tuning parameters for a given model “island” “We find that the major obstacle that hinders our understanding the brain is the fragmentation of brain research and the data it produces. Our most urgent need is thus a concerted international effort that can integrate this data in a unified picture of the brain as a single multi- level system...” The HBP-PS Consortium 2012:8 .
Recommended publications
  • Monitoring Synaptic and Neuronal Activity in 3D with Synthetic And
    Journal of Neuroscience Methods 222 (2014) 69–81 Contents lists available at ScienceDirect Journal of Neuroscience Methods jou rnal homepage: www.elsevier.com/locate/jneumeth Basic Neuroscience Monitoring synaptic and neuronal activity in 3D with synthetic and genetic indicators using a compact acousto-optic lens two-photon microscopeଝ Tomás Fernández-Alfonso, K.M. Naga Srinivas Nadella, M. Florencia Iacaruso, ∗ Bruno Pichler, Hana Ros,ˇ Paul A. Kirkby, R. Angus Silver Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK h i g h l i g h t s g r a p h i c a l a b s t r a c t • We expand the utility of acousto- optic lens (AOL) 3D 2P microscopy. • We show rapid, simultaneous moni- toring of synaptic inputs distributed in 3D. • First use of genetically encoded indicators with AOL 3D functional imaging. • Measurement of sensory-evoked neuronal population activity in 3D in vivo. • Strategies for improving the mea- surement of the timing of neuronal signals. a r t i c l e i n f o a b s t r a c t Article history: Background: Two-photon microscopy is widely used to study brain function, but conventional micro- Received 26 June 2013 scopes are too slow to capture the timing of neuronal signalling and imaging is restricted to one plane. Received in revised form 22 October 2013 Recent development of acousto-optic-deflector-based random access functional imaging has improved Accepted 26 October 2013 the temporal resolution, but the utility of these technologies for mapping 3D synaptic activity patterns and their performance at the excitation wavelengths required to image genetically encoded indicators Keywords: have not been investigated.
    [Show full text]
  • Physical Determinants of Vesicle Mobility and Supply at a Central
    RESEARCH ARTICLE Physical determinants of vesicle mobility and supply at a central synapse Jason Seth Rothman1, Laszlo Kocsis2, Etienne Herzog3,4, Zoltan Nusser2*, Robin Angus Silver1* 1Department of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom; 2Laboratory of Cellular Neurophysiology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary; 3Department of Molecular Neurobiology, Max Planck Institute of Experimental Medicine, Go¨ ttingen, Germany; 4Team Synapse in Cognition, Interdisciplinary Institute for Neuroscience, Universite´ de Bordeaux, UMR 5297, F-33000, Bordeaux, France Abstract Encoding continuous sensory variables requires sustained synaptic signalling. At several sensory synapses, rapid vesicle supply is achieved via highly mobile vesicles and specialized ribbon structures, but how this is achieved at central synapses without ribbons is unclear. Here we examine vesicle mobility at excitatory cerebellar mossy fibre synapses which sustain transmission over a broad frequency bandwidth. Fluorescent recovery after photobleaching in slices from VGLUT1Venus knock-in mice reveal 75% of VGLUT1-containing vesicles have a high mobility, comparable to that at ribbon synapses. Experimentally constrained models establish hydrodynamic interactions and vesicle collisions are major determinants of vesicle mobility in crowded presynaptic terminals. Moreover, models incorporating 3D reconstructions of vesicle clouds near active zones (AZs) predict the measured releasable pool size and replenishment rate from the reserve pool. They also show that while vesicle reloading at AZs is not diffusion-limited at the onset of release, *For correspondence: nusser@ diffusion limits vesicle reloading during sustained high-frequency signalling. koki.hu (ZN); [email protected] DOI: 10.7554/eLife.15133.001 (RAS) Competing interests: The authors declare that no competing interests exist.
    [Show full text]
  • Predominantly Linear Summation of Metabotropic Postsynaptic
    RESEARCH ARTICLE Predominantly linear summation of metabotropic postsynaptic potentials follows coactivation of neurogliaform interneurons Attila Ozsva´ r, Gergely Komlo´ si, Ga´ spa´ r Ola´ h, Judith Baka, Ga´ bor Molna´ r, Ga´ bor Tama´ s* MTA-SZTE Research Group for Cortical Microcircuits of the Hungarian Academy of Sciences,, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Szeged, Hungary Abstract Summation of ionotropic receptor-mediated responses is critical in neuronal computation by shaping input-output characteristics of neurons. However, arithmetics of summation for metabotropic signals are not known. We characterized the combined ionotropic and metabotropic output of neocortical neurogliaform cells (NGFCs) using electrophysiological and anatomical methods in the rat cerebral cortex. These experiments revealed that GABA receptors are activated outside release sites and confirmed coactivation of putative NGFCs in superficial cortical layers in vivo. Triple recordings from presynaptic NGFCs converging to a postsynaptic neuron revealed sublinear summation of ionotropic GABAA responses and linear summation of metabotropic GABAB responses. Based on a model combining properties of volume transmission and distributions of all NGFC axon terminals, we predict that in 83% of cases one or two NGFCs can provide input to a point in the neuropil. We suggest that interactions of metabotropic GABAergic responses remain linear even if most superficial layer interneurons specialized to recruit GABAB receptors are simultaneously active. *For correspondence: [email protected] Competing interests: The authors declare that no Introduction competing interests exist. Each neuron in the cerebral cortex receives thousands of excitatory synaptic inputs that drive action Funding: See page 20 potential (AP) output. The efficacy and timing of excitation is effectively governed by GABAergic Received: 10 December 2020 inhibitory inputs that arrive with spatiotemporal precision onto different subcellular domains.
    [Show full text]
  • Emmanuelle Chaigneau and Angus Silver
    Investigation of dendritic integration in spiny stellate cells of barrel cortex with 2-photon uncaging. E Chaigneau1 and RA Silver1 1. University College London, Department of Neuroscience, Physiology & Pharmacology, Gower street, London WC1E 6BT, United Kingdom Corresponding author: [email protected] Keywords: 2-photon microscopy, 2-photon photolysis, cortex Excitatory spiny neurons in layer 4 of somato-sensory exert a strong influence on transmission of information from the thalamus to the cortex [1] [2]. Their hyperpolarized resting potential [3] and relatively weak synaptic input [4] recorded in vivo raises the question of how they reach spike threshold. We have investigated how spiny stellate cells in barrel cortex integrate synaptic input by applying 2-photon uncaging in acute thalamocortical slices from P22-28 mice. To do this we patch loaded the cells with Alexa-594 and visualized the dendritic tree with 2-photon imaging. Layer 4 excitatory cells were identified on the basis of their location, anatomy and regular spiking firing properties. Different patterns of synaptic input onto the dendritic tree was mimicked at high spatiotemporal resolution by uncaging MNI-glutamate close to individual spines, while recording the membrane voltage through the somatic patch pipette. Under our experimental conditions, the resting potential of spiny stellate cells was -77 ± 7 mV (n = 52 cells). To ensure that the level of activation of synaptic glutamate receptors with photolysis was comparable to that during synaptic transmission, we first measured the quantal size of synaptic events which was -10 ± 2 pA (n = 4 cells). We then adjusted the photolysis laser power and duration so that the current evoked by uncaging MNI-glutamate on spines close to the cell soma, where dendritic filtering is minimized, matched the miniature current amplitude,.
    [Show full text]
  • 11-15 Juin 2014 Rapport Sur La Conférence
    Roscoff (France), 11-15 juin 2014 Imagerie (photonique) multi-échelle de la structure et de la fonction du cerveau Optical imaging of brain structure and function on multiple special scales PRESIDENT : Angus SILVER University College London, Londre, Royaume Uni VICE-PRESIDENT: Christophe MULLE CNRS UMR 5297, Université Bordeaux 2, Bordeaux, France Rapport sur la conférence Conference report RESUMÉ DU RAPPORT La Conférence Jacques Monod "Imagerie (photonique) multi-échelle de la structure et de la fonction du cerveau" s'est tenue à Roscoff du 11 au 15 juin 2014, sous la présidence du Prof Angus Silver (UCL, Londres) (vice-président, Christophe Mulle, DR CNRS, Bordeaux). Cette conférence internationale a rassemblé des experts mondialement reconnus de France, de différents pays d'Europe, des Etats-Unis et du Japon. Ils ont présenté les tous derniers développements technologiques et les découvertes sur l'analyse des synapses et des réseaux de neurones pour une meilleure compréhesion du fonctionnement du cerveau. La force de cette conférence est de mettre en relation étroite des neurobiologistes et des chercheurs actifs dans le développement de nouvelles technologies. L'analyse de la fonction du cerveau dépend étroitement des progrès en imagerie cellulaire sur le plan des sondes et des dispositifs instrumentaux, en techniques microscopiques super-résolutives, et de l'utilisation d'outils optogénétiques. Cette multidisciplinarité, qui fait la force et l'orginalité de cette conférence, a été unanimement appréciée par les participants, dont un nombre important de thésards et post-doctorants (70). Les organisateurs ont donné la possibilité à certains jeunes chercheurs (6) de présenter oralement leur travail. Les discussions ont été très riches durant les conférences et au cours des sessions de communications affichées et des multiples possibilités d'échanges informels.
    [Show full text]
  • Neuroscience and Mental Health UCL School of Life and Medical Sciences Creating Knowledge, Achieving Impact 3 PREFACE
    Neuroscience and Mental Health UCL SCHOOL OF LIFE AND MEDICAL SCIENCES Creating knowledge, achieving impact 3 PREFACE UCL’s School of Life and Medical Cluster (GMEC) for which we lead in Sciences encompasses arguably the the field of rare diseases. Our growing greatest concentration of biomedical collaboration with our Bloomsbury science and population health neighbours, the London School of expertise in Europe. Our performance Hygiene and Tropical Medicine, is in the UK’s last Research Assessment fuelling exciting developments in Exercise was outstanding, and for most genetic epidemiology and pathogen key measures the School comfortably research. tops UK league tables. The breadth and quality of our In part because of UCL’s size and research creates almost unique organisational complexity, the scale opportunities. Our recent merger with of the School’s achievements is not the London School of Pharmacy adds always apparent. This publication, to our capacity in drug development, one of four, seeks to address this. formulation and adoption. Our highly Our recent reorganisation, with the productive links to the health service, Basic Life Sciences: creation of four new Faculties, has through UCL Partners, provides 1 ‘Discovery’ research, from been designed to create a more access to unmatched clinical expertise molecules to ecosystems. coherent structure, of which the and large patient groups. We are Faculty of Life Sciences, headed by fortunate to be partners in three Translation and the Dean, Professor Mary Collins, National Institute for Health Research 2 Experimental Medicine: is a clear example. But the School’s (NIHR) Biomedical Research Centres restructuring has also placed great and a new NIHR Biomedical Research Driving translation to emphasis on cross-Faculty interactions Unit in dementia.
    [Show full text]
  • Deactivation and Desensitization of Non-NMDA Receptors in Patches and the Time Course of Epscs in Rat Cerebellar Granule Cells
    5404 Journal of Physiology (1996), 493.1, pp.167-173 167 Deactivation and desensitization of non-NMDA receptors in patches and the time course of EPSCs in rat cerebellar granule cells R. Angus Silver, David Colquhoun, Stuart G. Cull-Candy and Brian Edmonds Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK 1. Spontaneous and evoked non-NMDA receptor-mediated EPSCs were recorded from cerebellar granule cells in slices at -24 and -34 'C. The EPSC decay was fitted with the sum of two exponential functions. 2. The time courses of non-NMDA receptor deactivation and desensitization were determined with fast concentration jumps of glutamate onto patches from cultured granule cells. Deactivation (decay time constant r = 0 6 ms at 24 °C) was substantially faster than desensitization ('r = 4 ms). Both processes were fitted by single exponential functions. 3. The decay of the fast component of the spontaneous EPSC (TEPSCfast = 09 ms at 23 °C) was marginally slower than deactivation but too fast to be determined by desensitization. Our results suggest that the decay of this component is set by both the rate of decline of transmitter concentration and channel deactivation. 4. A simple diffusion model predicts that the time course of transmitter in the cleft declines slowly during the later stages of its action. The slow phase of transmitter removal could account for the time course of the slow component of the spontaneous EPSC (rEPscslow = 8 ms at 23°C). The time course of excitatory postsynaptic currents (EPSCs) the mossy fibre to granule cell EPSC (Silver, Traynelis & is determined by the time course of the concentration of Cull-Candy, 1992).
    [Show full text]
  • Neurobiology Technology
    TECHNOLOGY NEUROBIOLOGY times further down than two-photon imaging can, he says, although the limits depend on the properties of the tissue being imaged. His group managed to use the technique to image the mouse hippocampus, without removing any of the cortex above10. Xu’s team still can’t penetrate all the way through the brain — “We’re literally still scratching the surface,” he acknowledges — but there’s plenty of room for improvement, he says. There’s also room to develop live-brain imaging in other ways. A number of research- ers, including Kleinfeld and Svoboda, have devised systems that combine the wide mesoscopic field of view with the single-cell resolution achieved by two-photon imag- 4.0 NICHOLAS SOFRONIEW, DOI.ORG/10.7554/ELIFE.14472.015/CC BY ing, allowing them to zoom out on much of the brain or zoom in, Google Earth-style, on individual neurons11,12. Kleinfeld’s field- of-view covers an 8×10 millimetre section of cortex; Svoboda’s group can manage a cylinder of brain about 5 millimetres in diameter and 1 millimetre deep, and that’s about 25 times the typical field-of-view in two-photon micros- copy, he says. Svoboda has now trained several labs to build their own versions of his micro- scope, and licensed the technology to Thorlabs Two-photon microscopy can image cells as deep as 1 mm. These cortical neurons were imaged at 200 μm. in Newton, New Jersey. Ultimately, these diverse technologies of Colorado Anschutz Medical Campus of light. The technique can image one or two could realize Yuste’s dream for neuroscience: in Aurora.
    [Show full text]
  • Principles of Neural Design
    Principles of Neural Design Principles Compute with chemistry Compute directly with analog primitives Combine analog and pulsatile processing Sparsify Send only what is needed Send at the lowest acceptable rate Minimize wire Make neural components irreducibly small Complicate Adapt, match, learn, and forget Principles of Neural Design Peter Sterling and Simon Laughlin The MIT Press Cambridge, Massachusetts London, England © 2015 Massachusetts Institute of Technology All rights reserved. No part of this book may be reproduced in any form by any electronic or mechanical means (including photocopying, recording, or information storage and retrieval) without permission in writing from the publisher. MIT Press books may be purchased at special quantity discounts for business or sales promotional use. For information, please email [email protected]. This book was set in Stone Sans and Stone Serif by Toppan Best-set Premedia Limited. Printed and bound in the United States of America. Library of Congress Cataloging-in-Publication Data Sterling, Peter (Professor of neuroscience), author. Principles of neural design / Peter Sterling and Simon Laughlin. p. ; cm. Includes bibliographical references and index. ISBN 978-0-262-02870-7 (hardcover : alk. paper) I. Laughlin, Simon, author. II. Title. [DNLM: 1. Brain — physiology. 2. Learning. 3. Neural Pathways. WL 300] QP376 612.8’2 — dc23 2014031498 10 9 8 7 6 5 4 3 2 1 For Sally Zigmond and Barbara Laughlin Contents Preface ix Acknowledgments xi Introduction xiii 1 What Engineers Know about
    [Show full text]
  • Neurotechnology
    Imperial College Centre of Excellence in Neurotechnology BIENNIAL REPORT | 2017-2018 FOREWORD CENTRE FOR NEUROTECHNOLOGY DIRECTOR’S IMPERIAL COLLEGE LONDON FOREWORD ONE OF THE MAIN AIMS OF THE CENTRE FOR NEUROTECHNOLOGY has been to drive new collaborative research projects that span the range of disciplines represented at Imperial College and beyond, to improve our understanding of the brain and its disorders. PhD studentships have been one of the primary vessels for achieving this. The EPSRC Centre for Doctoral Training in Neurotechnology has taken two (or more) supervisors who bring complementary training expertise focussed at the intersection of neuroscience and engineering, and matched them with a stellar young PhD student to solve a difficult problem of real benefit to society. By any measure, this has been wildly successful, generating numerous new interdisciplinary collaborations, and providing these young scientist/engineers with a unique skillset which we expect to have great impact on the world. The new research collaborations generated by the Centre involve 31 principal investigators from 11 departments across the Faculties of Engineering, Life Sciences and Medicine. They have also spanned beyond Imperial, notably with the emergence of a strong collaboration on advanced closed-loop technology for deep brain stimulation, between Imperial, the University of Oxford, and Medtronic. THE CDT IS NOW IN ITS FIFTH YEAR, with the first cohort of students in the process of graduating – it gives me great pleasure to congratulate our first doctoral graduates, Cher Bass, Tamara Boltersdorf and Peter Quicke. The fifth and final cohort of students funded under this award began their research training www.imperial.ac.uk/neurotechnology in October 2018; they will graduate in 2022.
    [Show full text]
  • Acknowledgment of Reviewers, 2009
    Proceedings of the National Academy ofPNAS Sciences of the United States of America www.pnas.org Acknowledgment of Reviewers, 2009 The PNAS editors would like to thank all the individuals who dedicated their considerable time and expertise to the journal by serving as reviewers in 2009. Their generous contribution is deeply appreciated. A R. Alison Adcock Schahram Akbarian Paul Allen Lauren Ancel Meyers Duur Aanen Lia Addadi Brian Akerley Phillip Allen Robin Anders Lucien Aarden John Adelman Joshua Akey Fred Allendorf Jens Andersen Ruben Abagayan Zach Adelman Anna Akhmanova Robert Aller Olaf Andersen Alejandro Aballay Sarah Ades Eduard Akhunov Thorsten Allers Richard Andersen Cory Abate-Shen Stuart B. Adler Huda Akil Stefano Allesina Robert Andersen Abul Abbas Ralph Adolphs Shizuo Akira Richard Alley Adam Anderson Jonathan Abbatt Markus Aebi Gustav Akk Mark Alliegro Daniel Anderson Patrick Abbot Ueli Aebi Mikael Akke David Allison David Anderson Geoffrey Abbott Peter Aerts Armen Akopian Jeremy Allison Deborah Anderson L. Abbott Markus Affolter David Alais John Allman Gary Anderson Larry Abbott Pavel Afonine Eric Alani Laura Almasy James Anderson Akio Abe Jeffrey Agar Balbino Alarcon Osborne Almeida John Anderson Stephen Abedon Bharat Aggarwal McEwan Alastair Grac¸a Almeida-Porada Kathryn Anderson Steffen Abel John Aggleton Mikko Alava Genevieve Almouzni Mark Anderson Eugene Agichtein Christopher Albanese Emad Alnemri Richard Anderson Ted Abel Xabier Agirrezabala Birgit Alber Costica Aloman Robert P. Anderson Asa Abeliovich Ariel Agmon Tom Alber Jose´ Alonso Timothy Anderson Birgit Abler Noe¨l Agne`s Mark Albers Carlos Alonso-Alvarez Inger Andersson Robert Abraham Vladimir Agranovich Matthew Albert Suzanne Alonzo Tommy Andersson Wickliffe Abraham Anurag Agrawal Kurt Albertine Carlos Alos-Ferrer Masami Ando Charles Abrams Arun Agrawal Susan Alberts Seth Alper Tadashi Andoh Peter Abrams Rajendra Agrawal Adriana Albini Margaret Altemus Jose Andrade, Jr.
    [Show full text]
  • New Fellows and Foreign Members, Medals and Award Winners
    Promoting excellence in science 2017 New Fellows 2017 50 new Fellows, 10 new Foreign Members and one new Honorary Fellow were elected to the Society in May 2017 for their exceptional contributions to science. Individuals were elected from across the UK and Ireland, including Bristol, Aberdeen, Lancaster, Reading and Swansea, along with those from international institutions in Japan and the USA. New Fellows were admitted in July 2017 at the Admissions Ceremony, during which they signed the Charter Book. Professor Yves-Alain Professor Tony Bell FRS Professor Keith Beven Professor Wendy Professor Christopher Barde FRS FRS Bickmore FMedSci FRS Bishop FREng FRS Professor the Baroness Professor Neil Professor Krishna Professor James Mr Warren East CBE Brown of Cambridge Burgess FMedSci FRS Chatterjee FMedSci FRS Durrant FRS FREng FRS DBE FREng FRS Professor Tim Elliott Professor Anne Ferguson- Professor Jonathan Professor Mark Gross Professor Roy Harrison FRS Smith FMedSci FRS Gregory FRS FRS OBE FRS Professor Gabriele Professor Edward Professor Richard Professor Yvonne Jones Professor Subhash Khot Hegerl FRS Holmes FRS Houlston FMedSci FRS FMedSci FRS FRS Professor Stafford Professor Yadvinder Dr Andrew McKenzie Professor Gerard Professor Anne Neville Lightman FRS Malhi FRS FMedSci FRS Milburn FRS OBE FREng FRS Professor Alison Noble Professor Andrew Professor David Owen Professor Lawrence Professor Josephine OBE FREng FRS Orr-Ewing FRS FMedSci FRS Paulson FRS Pemberton FRS Professor Sandu Professor Sally Price Professor Anne Ridley Professor
    [Show full text]