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Dive into the research topics where Suzanna E. Lewis is active.

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Featured researches published by Suzanna E. Lewis.


Nature Genetics | 2000

Gene ontology: tool for the unification of biology. The Gene Ontology Consortium.

Michael Ashburner; Catherine A. Ball; Judith A. Blake; David Botstein; Heather L. Butler; J. Michael Cherry; Allan Peter Davis; Kara Dolinski; Selina S. Dwight; Janan T. Eppig; Midori A. Harris; David P. Hill; Laurie Issel-Tarver; Andrew Kasarskis; Suzanna E. Lewis; John C. Matese; Joel E. Richardson; Martin Ringwald; Gerald M. Rubin; Gavin Sherlock

Genomic sequencing has made it clear that a large fraction of the genes specifying the core biological functions are shared by all eukaryotes. Knowledge of the biological role of such shared proteins in one organism can often be transferred to other organisms. The goal of the Gene Ontology Consortium is to produce a dynamic, controlled vocabulary that can be applied to all eukaryotes even as knowledge of gene and protein roles in cells is accumulating and changing. To this end, three independent ontologies accessible on the World-Wide Web (http://www.geneontology.org) are being constructed: biological process, molecular function and cellular component.


Nucleic Acids Research | 2004

The Gene Ontology (GO) database and informatics resource.

Midori A. Harris; Jennifer I. Clark; Amelia Ireland; Jane Lomax; Michael Ashburner; R. Foulger; K. Eilbeck; Suzanna E. Lewis; B. Marshall; Christopher J. Mungall; John Richter; Gerald M. Rubin; Judith A. Blake; Mary E. Dolan; Harold J. Drabkin; Janan T. Eppig; David P. Hill; Li Ni; Martin Ringwald; Rama Balakrishnan; J. M. Cherry; Karen R. Christie; Maria C. Costanzo; Selina S. Dwight; Stacia R. Engel; Dianna G. Fisk; Jodi E. Hirschman; Eurie L. Hong; Robert S. Nash; Anand Sethuraman

The Gene Ontology (GO) project (http://www. geneontology.org/) provides structured, controlled vocabularies and classifications that cover several domains of molecular and cellular biology and are freely available for community use in the annotation of genes, gene products and sequences. Many model organism databases and genome annotation groups use the GO and contribute their annotation sets to the GO resource. The GO database integrates the vocabularies and contributed annotations and provides full access to this information in several formats. Members of the GO Consortium continually work collectively, involving outside experts as needed, to expand and update the GO vocabularies. The GO Web resource also provides access to extensive documentation about the GO project and links to applications that use GO data for functional analyses.


Nucleic Acids Research | 2004

Reactome: a knowledgebase of biological pathways

G. Joshi-Tope; Marc Gillespie; Imre Vastrik; Peter D'Eustachio; Esther Schmidt; B. de Bono; Bijay Jassal; G.R. Gopinath; G.R. Wu; Lisa Matthews; Suzanna E. Lewis; Ewan Birney; Lincoln Stein

Reactome, located at http://www.reactome.org is a curated, peer-reviewed resource of human biological processes. Given the genetic makeup of an organism, the complete set of possible reactions constitutes its reactome. The basic unit of the Reactome database is a reaction; reactions are then grouped into causal chains to form pathways. The Reactome data model allows us to represent many diverse processes in the human system, including the pathways of intermediary metabolism, regulatory pathways, and signal transduction, and high-level processes, such as the cell cycle. Reactome provides a qualitative framework, on which quantitative data can be superimposed. Tools have been developed to facilitate custom data entry and annotation by expert biologists, and to allow visualization and exploration of the finished dataset as an interactive process map. Although our primary curational domain is pathways from Homo sapiens, we regularly create electronic projections of human pathways onto other organisms via putative orthologs, thus making Reactome relevant to model organism research communities. The database is publicly available under open source terms, which allows both its content and its software infrastructure to be freely used and redistributed.


Bioinformatics | 2009

AmiGO: online access to ontology and annotation data

Seth Carbon; Amelia Ireland; Christopher J. Mungall; ShengQiang Shu; Brad Marshall; Suzanna E. Lewis

AmiGO is a web application that allows users to query, browse and visualize ontologies and related gene product annotation (association) data. AmiGO can be used online at the Gene Ontology (GO) website to access the data provided by the GO Consortium1; it can also be downloaded and installed to browse local ontologies and annotations.2 AmiGO is free open source software developed and maintained by the GO Consortium. Availability: http://amigo.geneontology.org Download: http://sourceforge.net/projects/geneontology/ Contact: [email protected]


Science | 2010

Identification of functional elements and regulatory circuits by Drosophila modENCODE

Sushmita Roy; Jason Ernst; Peter V. Kharchenko; Pouya Kheradpour; Nicolas Nègre; Matthew L. Eaton; Jane M. Landolin; Christopher A. Bristow; Lijia Ma; Michael F. Lin; Stefan Washietl; Bradley I. Arshinoff; Ferhat Ay; Patrick E. Meyer; Nicolas Robine; Nicole L. Washington; Luisa Di Stefano; Eugene Berezikov; Christopher D. Brown; Rogerio Candeias; Joseph W. Carlson; Adrian Carr; Irwin Jungreis; Daniel Marbach; Rachel Sealfon; Michael Y. Tolstorukov; Sebastian Will; Artyom A. Alekseyenko; Carlo G. Artieri; Benjamin W. Booth

From Genome to Regulatory Networks For biologists, having a genome in hand is only the beginning—much more investigation is still needed to characterize how the genome is used to help to produce a functional organism (see the Perspective by Blaxter). In this vein, Gerstein et al. (p. 1775) summarize for the Caenorhabditis elegans genome, and The modENCODE Consortium (p. 1787) summarize for the Drosophila melanogaster genome, full transcriptome analyses over developmental stages, genome-wide identification of transcription factor binding sites, and high-resolution maps of chromatin organization. Both studies identified regions of the nematode and fly genomes that show highly occupied targets (or HOT) regions where DNA was bound by more than 15 of the transcription factors analyzed and the expression of related genes were characterized. Overall, the studies provide insights into the organization, structure, and function of the two genomes and provide basic information needed to guide and correlate both focused and genome-wide studies. The Drosophila modENCODE project demonstrates the functional regulatory network of flies. To gain insight into how genomic information is translated into cellular and developmental programs, the Drosophila model organism Encyclopedia of DNA Elements (modENCODE) project is comprehensively mapping transcripts, histone modifications, chromosomal proteins, transcription factors, replication proteins and intermediates, and nucleosome properties across a developmental time course and in multiple cell lines. We have generated more than 700 data sets and discovered protein-coding, noncoding, RNA regulatory, replication, and chromatin elements, more than tripling the annotated portion of the Drosophila genome. Correlated activity patterns of these elements reveal a functional regulatory network, which predicts putative new functions for genes, reveals stage- and tissue-specific regulators, and enables gene-expression prediction. Our results provide a foundation for directed experimental and computational studies in Drosophila and related species and also a model for systematic data integration toward comprehensive genomic and functional annotation.


Nucleic Acids Research | 2009

Reactome knowledgebase of human biological pathways and processes.

Lisa Matthews; Gopal Gopinath; Marc Gillespie; Michael Caudy; David Croft; Bernard de Bono; Phani Garapati; Jill Hemish; Henning Hermjakob; Bijay Jassal; Alex Kanapin; Suzanna E. Lewis; Shahana Mahajan; Bruce May; Esther Schmidt; Imre Vastrik; Guanming Wu; Ewan Birney; Lincoln Stein; Peter D’Eustachio

Reactome (http://www.reactome.org) is an expert-authored, peer-reviewed knowledgebase of human reactions and pathways that functions as a data mining resource and electronic textbook. Its current release includes 2975 human proteins, 2907 reactions and 4455 literature citations. A new entity-level pathway viewer and improved search and data mining tools facilitate searching and visualizing pathway data and the analysis of user-supplied high-throughput data sets. Reactome has increased its utility to the model organism communities with improved orthology prediction methods allowing pathway inference for 22 species and through collaborations to create manually curated Reactome pathway datasets for species including Arabidopsis, Oryza sativa (rice), Drosophila and Gallus gallus (chicken). Reactomes data content and software can all be freely used and redistributed under open source terms.


Nature | 2001

Functional annotation of a full-length mouse cDNA collection

Jun Kawai; Akira Shinagawa; Kazuhiro Shibata; Masataka Yoshino; Masayoshi Itoh; Yoshiyuki Ishii; Takahiro Arakawa; Ayako Hara; Yoshifumi Fukunishi; Hideaki Konno; Jun Adachi; Shiro Fukuda; Katsunori Aizawa; Masaki Izawa; Kenichiro Nishi; Hidenori Kiyosawa; Shinji Kondo; Itaru Yamanaka; Tsuyoshi Saito; Yasushi Okazaki; Takashi Gojobori; Hidemasa Bono; Takeya Kasukawa; R. Saito; Koji Kadota; Hideo Matsuda; Michael Ashburner; Serge Batalov; Tom L. Casavant; W. Fleischmann

The RIKEN Mouse Gene Encyclopaedia Project, a systematic approach to determining the full coding potential of the mouse genome, involves collection and sequencing of full-length complementary DNAs and physical mapping of the corresponding genes to the mouse genome. We organized an international functional annotation meeting (FANTOM) to annotate the first 21,076 cDNAs to be analysed in this project. Here we describe the first RIKEN clone collection, which is one of the largest described for any organism. Analysis of these cDNAs extends known gene families and identifies new ones.The RIKEN Mouse Gene Encyclopaedia Project, a systematic approach to determining the full coding potential of the mouse genome, involves collection and sequencing of full-length complementary DNAs and physical mapping of the corresponding genes to the mouse genome. We organized an international functional annotation meeting (FANTOM) to annotate the first 21,076 cDNAs to be analysed in this project. Here we describe the first RIKEN clone collection, which is one of the largest described for any organism. Analysis of these cDNAs extends known gene families and identifies new ones.


Genome Biology | 2002

Systematic determination of patterns of gene expression during Drosophila embryogenesis

Pavel Tomancak; Amy Beaton; Richard Weiszmann; Elaine Kwan; ShengQiang Shu; Suzanna E. Lewis; Stephen Richards; Michael Ashburner; Volker Hartenstein; Susan E. Celniker; Gerald M. Rubin

BackgroundCell-fate specification and tissue differentiation during development are largely achieved by the regulation of gene transcription.ResultsAs a first step to creating a comprehensive atlas of gene-expression patterns during Drosophila embryogenesis, we examined 2,179 genes by in situ hybridization to fixed Drosophila embryos. Of the genes assayed, 63.7% displayed dynamic expression patterns that were documented with 25,690 digital photomicrographs of individual embryos. The photomicrographs were annotated using controlled vocabularies for anatomical structures that are organized into a developmental hierarchy. We also generated a detailed time course of gene expression during embryogenesis using microarrays to provide an independent corroboration of the in situ hybridization results. All image, annotation and microarray data are stored in publicly available database. We found that the RNA transcripts of about 1% of genes show clear subcellular localization. Nearly all the annotated expression patterns are distinct. We present an approach for organizing the data by hierarchical clustering of annotation terms that allows us to group tissues that express similar sets of genes as well as genes displaying similar expression patterns.ConclusionsAnalyzing gene-expression patterns by in situ hybridization to whole-mount embryos provides an extremely rich dataset that can be used to identify genes involved in developmental processes that have been missed by traditional genetic analysis. Systematic analysis of rigorously annotated patterns of gene expression will complement and extend the types of analyses carried out using expression microarrays.


Genome Biology | 2005

The Sequence Ontology: a tool for the unification of genome annotations

Karen Eilbeck; Suzanna E. Lewis; Christopher J. Mungall; Mark Yandell; Lincoln Stein; Richard Durbin; Michael Ashburner

The Sequence Ontology (SO) is a structured controlled vocabulary for the parts of a genomic annotation. SO provides a common set of terms and definitions that will facilitate the exchange, analysis and management of genomic data. Because SO treats part-whole relationships rigorously, data described with it can become substrates for automated reasoning, and instances of sequence features described by the SO can be subjected to a group of logical operations termed extensional mereology operators.


Nucleic Acids Research | 2008

The Gene Ontology project in 2008

Midori A. Harris; Jennifer I. Deegan; Amelia Ireland; Jane Lomax; Michael Ashburner; Susan Tweedie; Seth Carbon; Suzanna E. Lewis; Christopher J. Mungall; John Richter; Karen Eilbeck; Judith A. Blake; Alexander D. Diehl; Mary E. Dolan; Harold Drabkin; Janan T. Eppig; David P. Hill; Ni Li; Martin Ringwald; Rama Balakrishnan; Gail Binkley; J. Michael Cherry; Karen R. Christie; Maria C. Costanzo; Qing Dong; Stacia R. Engel; Dianna G. Fisk; Jodi E. Hirschman; Benjamin C. Hitz; Eurie L. Hong

The Gene Ontology (GO) project (http://www.geneontology.org/) provides a set of structured, controlled vocabularies for community use in annotating genes, gene products and sequences (also see http://www.sequenceontology.org/). The ontologies have been extended and refined for several biological areas, and improvements to the structure of the ontologies have been implemented. To improve the quantity and quality of gene product annotations available from its public repository, the GO Consortium has launched a focused effort to provide comprehensive and detailed annotation of orthologous genes across a number of ‘reference’ genomes, including human and several key model organisms. Software developments include two releases of the ontology-editing tool OBO-Edit, and improvements to the AmiGO browser interface.

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Christopher J. Mungall

Lawrence Berkeley National Laboratory

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Gerald M. Rubin

Howard Hughes Medical Institute

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Nicole L. Washington

Lawrence Berkeley National Laboratory

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Damian Smedley

Queen Mary University of London

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Lincoln Stein

Ontario Institute for Cancer Research

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Sebastian Köhler

Lawrence Berkeley National Laboratory

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