A Twentieth Anniversary Tribute to Psb
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RECENT ADVANCES in BIOLOGY, BIOPHYSICS, BIOENGINEERING and COMPUTATIONAL CHEMISTRY
RECENT ADVANCES in BIOLOGY, BIOPHYSICS, BIOENGINEERING and COMPUTATIONAL CHEMISTRY Proceedings of the 5th WSEAS International Conference on CELLULAR and MOLECULAR BIOLOGY, BIOPHYSICS and BIOENGINEERING (BIO '09) Proceedings of the 3rd WSEAS International Conference on COMPUTATIONAL CHEMISTRY (COMPUCHEM '09) Puerto De La Cruz, Tenerife, Canary Islands, Spain December 14-16, 2009 Recent Advances in Biology and Biomedicine A Series of Reference Books and Textbooks Published by WSEAS Press ISSN: 1790-5125 www.wseas.org ISBN: 978-960-474-141-0 RECENT ADVANCES in BIOLOGY, BIOPHYSICS, BIOENGINEERING and COMPUTATIONAL CHEMISTRY Proceedings of the 5th WSEAS International Conference on CELLULAR and MOLECULAR BIOLOGY, BIOPHYSICS and BIOENGINEERING (BIO '09) Proceedings of the 3rd WSEAS International Conference on COMPUTATIONAL CHEMISTRY (COMPUCHEM '09) Puerto De La Cruz, Tenerife, Canary Islands, Spain December 14-16, 2009 Recent Advances in Biology and Biomedicine A Series of Reference Books and Textbooks Published by WSEAS Press www.wseas.org Copyright © 2009, by WSEAS Press All the copyright of the present book belongs to the World Scientific and Engineering Academy and Society Press. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without the prior written permission of the Editor of World Scientific and Engineering Academy and Society Press. All papers of the present volume were peer reviewed -
Proquest Dissertations
Automated learning of protein involvement in pathogenesis using integrated queries Eithon Cadag A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy University of Washington 2009 Program Authorized to Offer Degree: Department of Medical Education and Biomedical Informatics UMI Number: 3394276 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. UMI Dissertation Publishing UMI 3394276 Copyright 2010 by ProQuest LLC. All rights reserved. This edition of the work is protected against unauthorized copying under Title 17, United States Code. uest ProQuest LLC 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106-1346 University of Washington Graduate School This is to certify that I have examined this copy of a doctoral dissertation by Eithon Cadag and have found that it is complete and satisfactory in all respects, and that any and all revisions required by the final examining committee have been made. Chair of the Supervisory Committee: Reading Committee: (SjLt KJ. £U*t~ Peter Tgffczy-Hornoch In presenting this dissertation in partial fulfillment of the requirements for the doctoral degree at the University of Washington, I agree that the Library shall make its copies freely available for inspection. I further agree that extensive copying of this dissertation is allowable only for scholarly purposes, consistent with "fair use" as prescribed in the U.S. -
Molecular Biology for Computer Scientists
CHAPTER 1 Molecular Biology for Computer Scientists Lawrence Hunter “Computers are to biology what mathematics is to physics.” — Harold Morowitz One of the major challenges for computer scientists who wish to work in the domain of molecular biology is becoming conversant with the daunting intri- cacies of existing biological knowledge and its extensive technical vocabu- lary. Questions about the origin, function, and structure of living systems have been pursued by nearly all cultures throughout history, and the work of the last two generations has been particularly fruitful. The knowledge of liv- ing systems resulting from this research is far too detailed and complex for any one human to comprehend. An entire scientific career can be based in the study of a single biomolecule. Nevertheless, in the following pages, I attempt to provide enough background for a computer scientist to understand much of the biology discussed in this book. This chapter provides the briefest of overviews; I can only begin to convey the depth, variety, complexity and stunning beauty of the universe of living things. Much of what follows is not about molecular biology per se. In order to 2ARTIFICIAL INTELLIGENCE & MOLECULAR BIOLOGY explain what the molecules are doing, it is often necessary to use concepts involving, for example, cells, embryological development, or evolution. Bi- ology is frustratingly holistic. Events at one level can effect and be affected by events at very different levels of scale or time. Digesting a survey of the basic background material is a prerequisite for understanding the significance of the molecular biology that is described elsewhere in the book. -
Department of Energy Office of Health and Environmental Research SEQUENCING the HUMAN GENOME Summary Report of the Santa Fe Workshop March 3-4, 1986
Department of Energy Office of Health and Environmental Research SEQUENCING THE HUMAN GENOME Summary Report of the Santa Fe Workshop March 3-4, 1986 Los Alamos National Laboratory Los Alamos Los Alamos, New Mexico 87545 Los Alamos National Laboratory is operated by the University of California for the United States Department of Energy under contract W-7405-ENG-36. DEPARTMENT OF ENERGY OFFICE OF HEALTH AND ENVIRONMENTAL RESEARCH SEQUENCING THE HUMAN GENOME SUMMARY REPORT ON THE SANTA FE WORKSHOP (MARCH 3-4, 1986) Executive Summary. The following is a summary of the Santa Fe Workshop held on March 3 and 4, 1986. The workshop was sponsored by the Office of Health and Environmental Research (OHER) and Los Alamos National Laboratory (LANL) and dedicated to examining the feasibility, advisability, and approaches to sequencing the human genome. The workshop considered four principal topics: I. Technologies to be employed. II. Expected benefits. III. Architecture of the enterprise. IV. Participants and funding. I . Technology The participants of the workshop foresaw extraordinary and continuing progress in the efficiency and accuracy of mapping, ordering , and sequencing technologies. They suggested that a coordinated analysis of the human genome begin with the task of ordering overlapping recombinant DNA fragments obtained from purified human chromosomes that would provide an infrastructure for sequencing activity. At the same time, they support in-depth evaluation of current and developing strategies for sequencing including possible applications of automation and robotics that would minimize the time and cost of sequencing. II. Benefits The socio-political and health benefits, and the benefit:cost ratio were seen as highly favorable not only for human health, but in addition for the development of new diagnostic, preventative and therapeutic tools, jobs, and industries. -
Ontology-Based Methods for Analyzing Life Science Data
Habilitation a` Diriger des Recherches pr´esent´ee par Olivier Dameron Ontology-based methods for analyzing life science data Soutenue publiquement le 11 janvier 2016 devant le jury compos´ede Anita Burgun Professeur, Universit´eRen´eDescartes Paris Examinatrice Marie-Dominique Devignes Charg´eede recherches CNRS, LORIA Nancy Examinatrice Michel Dumontier Associate professor, Stanford University USA Rapporteur Christine Froidevaux Professeur, Universit´eParis Sud Rapporteure Fabien Gandon Directeur de recherches, Inria Sophia-Antipolis Rapporteur Anne Siegel Directrice de recherches CNRS, IRISA Rennes Examinatrice Alexandre Termier Professeur, Universit´ede Rennes 1 Examinateur 2 Contents 1 Introduction 9 1.1 Context ......................................... 10 1.2 Challenges . 11 1.3 Summary of the contributions . 14 1.4 Organization of the manuscript . 18 2 Reasoning based on hierarchies 21 2.1 Principle......................................... 21 2.1.1 RDF for describing data . 21 2.1.2 RDFS for describing types . 24 2.1.3 RDFS entailments . 26 2.1.4 Typical uses of RDFS entailments in life science . 26 2.1.5 Synthesis . 30 2.2 Case study: integrating diseases and pathways . 31 2.2.1 Context . 31 2.2.2 Objective . 32 2.2.3 Linking pathways and diseases using GO, KO and SNOMED-CT . 32 2.2.4 Querying associated diseases and pathways . 33 2.3 Methodology: Web services composition . 39 2.3.1 Context . 39 2.3.2 Objective . 40 2.3.3 Semantic compatibility of services parameters . 40 2.3.4 Algorithm for pairing services parameters . 40 2.4 Application: ontology-based query expansion with GO2PUB . 43 2.4.1 Context . 43 2.4.2 Objective . -
Mapping Our Genes—Genome Projects: How Big? How Fast?
Mapping Our Genes—Genome Projects: How Big? How Fast? April 1988 NTIS order #PB88-212402 Recommended Citation: U.S. Congress, Office of Technology Assessment, Mapping Our Genes-The Genmne Projects.’ How Big, How Fast? OTA-BA-373 (Washington, DC: U.S. Government Printing Office, April 1988). Library of Congress Catalog Card Number 87-619898 For sale by the Superintendent of Documents U.S. Government Printing Office, Washington, DC 20402-9325 (order form can be found in the back of this report) Foreword For the past 2 years, scientific and technical journals in biology and medicine have extensively covered a debate about whether and how to determine the function and order of human genes on human chromosomes and when to determine the sequence of molecular building blocks that comprise DNA in those chromosomes. In 1987, these issues rose to become part of the public agenda. The debate involves science, technol- ogy, and politics. Congress is responsible for ‘(writing the rules” of what various Federal agencies do and for funding their work. This report surveys the points made so far in the debate, focusing on those that most directly influence the policy options facing the U.S. Congress, The House Committee on Energy and Commerce requested that OTA undertake the project. The House Committee on Science, Space, and Technology, the Senate Com- mittee on Labor and Human Resources, and the Senate Committee on Energy and Natu- ral Resources also asked OTA to address specific points of concern to them. Congres- sional interest focused on several issues: ● how to assess the rationales for conducting human genome projects, ● how to fund human genome projects (at what level and through which mech- anisms), ● how to coordinate the scientific and technical programs of the several Federal agencies and private interests already supporting various genome projects, and ● how to strike a balance regarding the impact of genome projects on international scientific cooperation and international economic competition in biotechnology. -
Program Book
Pacific Symposium on Biocomputing 2016 January 4-8, 2016 Big Island of Hawaii Program Book PACIFIC SYMPOSIUM ON BIOCOMPUTING 2016 Big Island of Hawaii, January 4-8, 2016 Welcome to PSB 2016! We have prepared this program book to give you quick access to information you need for PSB 2016. Enclosed you will find • Logistics information • Menus for PSB hosted meals • Full conference schedule • Call for Session and Workshop Proposals for PSB 2017 • Poster/abstract titles and authors • Participant List Conference materials are also available online at http://psb.stanford.edu/conference-materials/. PSB 2016 gratefully acknowledges the support the Institute for Computational Biology, a collaborative effort of Case Western Reserve University, the Cleveland Clinic Foundation, and University Hospitals; the National Institutes of Health (NIH), the National Science Foundation (NSF); and the International Society for Computational Biology (ISCB). If you or your institution are interested in sponsoring, PSB, please contact Tiffany Murray at [email protected] If you have any questions, the PSB registration staff (Tiffany Murray, Georgia Hansen, Brant Hansen, Kasey Miller, and BJ Morrison-McKay) are happy to help you. Aloha! Russ Altman Keith Dunker Larry Hunter Teri Klein Maryln Ritchie The PSB 2016 Organizers PACIFIC SYMPOSIUM ON BIOCOMPUTING 2016 Big Island of Hawaii, January 4-8, 2016 SPEAKER INFORMATION Oral presentations of accepted proceedings papers will take place in Salon 2 & 3. Speakers are allotted 10 minutes for presentation and 5 minutes for questions for a total of 15 minutes. Instructions for uploading talks were sent to authors with oral presentations. If you need assistance with this, please see Tiffany Murray or another PSB staff member. -
Conference Proceedingssmall
1 COMMITTEES Steering Committee Phil Bourne - University of California, San Diego Eric Davidson - California Institute of Technology Steven Salzberg - The Institute for Genomic Research John Wooley - University of California San Diego, San Diego Supercomputer Center Organizing Committee Pat Blauvelt – LSS Membership Director Karen Hauge – Palo Alto Medical Foundation, Local Arangements Kass Goldfein - Finance Consultant AlishaHolloway – The J. David Gladstone Institutes, Tutorial Chair Sami Khuri – San Jose State University, Poster Chair Ann Loraine – University of North Carolina at Charlotte, CSB Publication Chair Fenglou Mao – University of Georgia, On-Line Registration and Refereeing Website Peter Markstein – in silico Labs, Program Co-Chair Vicky Markstein - Life Sciences Society, Conference Chair, LSS President Jean Tsukamoto - Graphics Design Bill Wang - Sun Microsystems Inc, LSS Information Technology Director Ying Xu – University of Georgia, Program Co-Chair Program Committee Tatsuya Akutsu – Kyoto University Chris Bailey-Kellogg – Dartmouth College Pierre Baldi – University of California Irvine Liming Cai – University of Georgia Bill Cannon – Pacific Northwest National Laboratory Jake Chen – Indiana University Bhaskar DasGupta – University of Illinois Chicago Andrey Gorin – Oak Ridge National Laboratory Matt Hibbs – Princeton University Wen-Lian Hsu – Academia Sinica Tamer Kahveci – University of Florida Carl Kingsford – University of Maryland Christina Leslie – Memorial Sloan-Kettering Cancer Center Jing Li – Case Western Reserve -
Characterizing the Dna-Binding Site Specificities of Cis2his2 Zinc Fingers
MQP-ID-DH-UM1 C H A R A C T E RI Z IN G T H E DN A-BINDIN G SI T E SPE C I F I C I T I ES O F C IS2H IS2 Z IN C F IN G E RS A Major Qualifying Project Report Submitted to the Faculty of the WORCESTER POLYTECHNIC INSTITUTE in partial fulfillment of the requirements for the Degrees of Bachelor of Science in Biochemistry and Biology and Biotechnology by _________________________ Heather Bell April 26, 2012 APPROVED: ____________________ ____________________ ____________________ Scot Wolfe, PhD Destin Heilman, PhD David Adams, PhD Gene Function and Exp. Biochemistry Biology and Biotech UMass Medical School WPI Project Advisor WPI Project Advisor MAJOR ADVISOR A BST R A C T The ability to modularly assemble Zinc Finger Proteins (ZFPs) as well as the wide variety of DNA sequences they can recognize, make ZFPs an ideal framework to design novel DNA-binding proteins. However, due to the complexity of the interactions between residues in the ZF recognition helix and the DNA-binding site there is currently no comprehensive recognition code that would allow for the accurate prediction of the DNA ZFP binding motifs or the design of novel ZFPs for a desired target site. Through the analysis of the DNA-binding site specificities of 98 ZFP clones, determined through a bacterial one-hybrid selection system, a predictive model was created that can accurately predict the binding site motifs of novel ZFPs. 2 T A B L E O F C O N T E N TS Signature Page ««««««««««««««««««««««««««« $EVWUDFW«««««««««««««««««««««««««««««« 7DEOHRI&RQWHQWV«««««««««««««««««««««««««« $FNQRZOHGJHPHQWV««««««««««««««««««««««««« %DFNJURXQG«««««««««««««««««««««««««««« Project Purpose «««««««««««««««««««««««««««15 0HWKRGV««««««««««««««««««««««««««««««16 5HVXOWV««««««««««««««««««««««««««««««21 'LVFXVVLRQ«««««««««««««««««««««««««««««28 Bibliograph\«««««««««««««««««««««««««««« 6XSSOHPHQWDO««««««««««««««««««««««««««« 3 A C K N O W L E D G E M E N TS I would like to thank Dr. -
2015 Wattiezm Memoire
Institutional Repository - Research Portal Dépôt Institutionnel - Portail de la Recherche University of Namurresearchportal.unamur.be THESIS / THÈSE MASTER IN COMPUTER SCIENCE Design of a support system for modelling gene regulatory networks Author(s) - Auteur(s) : Wattiez, Morgan Award date: 2015 Awarding institution: University of Namur Supervisor - Co-Supervisor / Promoteur - Co-Promoteur : Link to publication Publication date - Date de publication : Permanent link - Permalien : Rights / License - Licence de droit d’auteur : General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal ? Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. BibliothèqueDownload date: Universitaire 04. oct.. 2021 Moretus Plantin University of Namur Faculty of Computer Science Academic Year 2014{2015 Design of a support system for modelling gene regulatory networks Morgan WATTIEZ Supervisor: (Signed for Release Approval Jean-Marie JACQUET Study Rules art. 40) Thesis submitted in partial fulfillment of the requirements for the degree of Master in Computer Science at the University of Namur Abstract The understanding of gene regulatory networks depends upon the solving of ques- tions related to the interactions in those networks. -
UC Irvine UC Irvine Previously Published Works
UC Irvine UC Irvine Previously Published Works Title The capacity of feedforward neural networks. Permalink https://escholarship.org/uc/item/29h5t0hf Authors Baldi, Pierre Vershynin, Roman Publication Date 2019-08-01 DOI 10.1016/j.neunet.2019.04.009 License https://creativecommons.org/licenses/by/4.0/ 4.0 Peer reviewed eScholarship.org Powered by the California Digital Library University of California THE CAPACITY OF FEEDFORWARD NEURAL NETWORKS PIERRE BALDI AND ROMAN VERSHYNIN Abstract. A long standing open problem in the theory of neural networks is the devel- opment of quantitative methods to estimate and compare the capabilities of different ar- chitectures. Here we define the capacity of an architecture by the binary logarithm of the number of functions it can compute, as the synaptic weights are varied. The capacity provides an upperbound on the number of bits that can be extracted from the training data and stored in the architecture during learning. We study the capacity of layered, fully-connected, architectures of linear threshold neurons with L layers of size n1, n2,...,nL and show that in essence the capacity is given by a cubic polynomial in the layer sizes: L−1 C(n1,...,nL) = Pk=1 min(n1,...,nk)nknk+1, where layers that are smaller than all pre- vious layers act as bottlenecks. In proving the main result, we also develop new techniques (multiplexing, enrichment, and stacking) as well as new bounds on the capacity of finite sets. We use the main result to identify architectures with maximal or minimal capacity under a number of natural constraints. -
Two-Page PDF Version
CALL FOR PAPERS IEEE Computer Society Bioinformatics Conference Stanford University, Stanford, CA August 11–14, 2003 You are invited to submit a paper to the 2003 IEEE Computer Society Bioinformatics Conference (CSB2003). The conference’s goal is to facilitate collaboration between com- puter scientists and biologists by presenting cutting edge computational biology research findings. While such research has an interdisciplinary character, CSB2003 emphasizes the computational aspects of bioinformatics research. Computer science papers must show bio- logical relevance, and biology papers must stress the computational aspects of the results. CSB2003 will accept 27 papers for podium presentation, and these will be published in the IEEE conference proceedings. Topics of interest include (but are not limited to): • Machine Learning • String & Graph Algorithms • Data Mining • Genome to Life • Robotics • Stochastic Modeling • Data Visualization • Genomics and Proteomics • Regulatory Networks • Gene Expression Pathways • Comparative Genomics • Evolution and Phylogenetics • Pattern Recognition • Molecular Structures & Interactions Papers are limited to 12 pages, single spaced, in 12 point type, including title, abstract (250 words or less), figures, tables, text, and bibliography. The first page should give keywords, authors’ postal and electronic mailing addresses. Submit papers electronically to bioinfor- [email protected] in either postscript or PDF format. A select subset of accepted papers will be invited to also publish in the Journal of Bioinformatics and Computational Biology (http://www.worldscinet.com/jbcb/jbcb.shtml). The Best Paper will be selected by the Program Committee and announced at the awards ceremony. Submissions must be received no later than April 1, 2003. Authors will be notified of their submission's status by May 19, 2003, and final corrected versions must be received by June 14, 2003.