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Featured researches published by Peter Sterk.


Nature Biotechnology | 2008

Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project

Chris F. Taylor; Dawn Field; Susanna-Assunta Sansone; Jan Aerts; Rolf Apweiler; Michael Ashburner; Catherine A. Ball; Pierre Alain Binz; Molly Bogue; Tim Booth; Alvis Brazma; Ryan R. Brinkman; Adam Clark; Eric W. Deutsch; Oliver Fiehn; Jennifer Fostel; Peter Ghazal; Frank Gibson; Tanya Gray; Graeme Grimes; John M. Hancock; Nigel Hardy; Henning Hermjakob; Randall K. Julian; Matthew Kane; Carsten Kettner; Christopher R. Kinsinger; Eugene Kolker; Martin Kuiper; Nicolas Le Novère

The Minimum Information for Biological and Biomedical Investigations (MIBBI) project aims to foster the coordinated development of minimum-information checklists and provide a resource for those exploring the range of extant checklists.


Science | 2009

Genome Project Standards in a New Era of Sequencing

Patrick Chain; Darren Grafham; Robert S. Fulton; Michael Fitzgerald; Jessica B. Hostetler; Donna M. Muzny; J. Ali; Bruce W. Birren; David Bruce; Christian Buhay; James R. Cole; Yan Ding; Shannon Dugan; Dawn Field; George M Garrity; Richard A. Gibbs; Tina Graves; Cliff Han; Scott H. Harrison; Sarah K. Highlander; Philip Hugenholtz; H. M. Khouri; Chinnappa D. Kodira; Eugene Kolker; Nikos C. Kyrpides; D. Lang; Alla Lapidus; S. A. Malfatti; Victor Markowitz; T. Metha

More detailed sequence standards that keep up with revolutionary sequencing technologies will aid the research community in evaluating data. For over a decade, genome sequences have adhered to only two standards that are relied on for purposes of sequence analysis by interested third parties (1, 2). However, ongoing developments in revolutionary sequencing technologies have resulted in a redefinition of traditional whole-genome sequencing that requires reevaluation of such standards. With commercially available 454 pyrosequencing (followed by Illumina, SOLiD, and now Helicos), there has been an explosion of genomes sequenced under the moniker “draft”; however, these can be very poor quality genomes (due to inherent errors in the sequencing technologies, and the inability of assembly programs to fully address these errors). Further, one can only infer that such draft genomes may be of poor quality by navigating through the databases to find the number and type of reads deposited in sequence trace repositories (and not all genomes have this available), or to identify the number of contigs or genome fragments deposited to the database. The difficulty in assessing the quality of such deposited genomes has created some havoc for genome analysis pipelines and has contributed to many wasted hours. Exponential leaps in raw sequencing capability and greatly reduced prices have further skewed the time- and cost-ratios of draft data generation versus the painstaking process of improving and finishing a genome. The result is an ever-widening gap between drafted and finished genomes that only promises to continue (see the figure, page 236); hence, there is an urgent need to distinguish good from poor data sets.


Bioinformatics | 2010

ISA software suite

Philippe Rocca-Serra; Marco Brandizi; Eamonn Maguire; Nataliya Sklyar; Chris F. Taylor; Kimberly Begley; Dawn Field; Stephen Harris; Winston Hide; Oliver Hofmann; Steffen Neumann; Peter Sterk; Weida Tong; Susanna-Assunta Sansone

Summary: The first open source software suite for experimentalists and curators that (i) assists in the annotation and local management of experimental metadata from high-throughput studies employing one or a combination of omics and other technologies; (ii) empowers users to uptake community-defined checklists and ontologies; and (iii) facilitates submission to international public repositories. Availability and Implementation: Software, documentation, case studies and implementations at http://www.isa-tools.org Contact: [email protected]


Nucleic Acids Research | 2014

EBI metagenomics—a new resource for the analysis and archiving of metagenomic data

Sarah Hunter; Matthew Corbett; Hubert Denise; Matthew Fraser; Alejandra Gonzalez-Beltran; Chris Hunter; Philip Jones; Rasko Leinonen; Craig McAnulla; Eamonn Maguire; John Maslen; Alex L. Mitchell; Gift Nuka; Arnaud Oisel; Sebastien Pesseat; Rajesh Radhakrishnan; Philippe Rocca-Serra; Maxim Scheremetjew; Peter Sterk; Daniel Vaughan; Guy Cochrane; Dawn Field; Susanna-Assunta Sansone

Metagenomics is a relatively recently established but rapidly expanding field that uses high-throughput next-generation sequencing technologies to characterize the microbial communities inhabiting different ecosystems (including oceans, lakes, soil, tundra, plants and body sites). Metagenomics brings with it a number of challenges, including the management, analysis, storage and sharing of data. In response to these challenges, we have developed a new metagenomics resource (http://www.ebi.ac.uk/metagenomics/) that allows users to easily submit raw nucleotide reads for functional and taxonomic analysis by a state-of-the-art pipeline, and have them automatically stored (together with descriptive, standards-compliant metadata) in the European Nucleotide Archive.


Nucleic Acids Research | 2016

EBI metagenomics in 2016--an expanding and evolving resource for the analysis and archiving of metagenomic data.

Alex L. Mitchell; François Bucchini; Guy Cochrane; Hubert Denise; Petra ten Hoopen; Matthew Fraser; Sebastien Pesseat; Simon Potter; Maxim Scheremetjew; Peter Sterk; Robert D. Finn

EBI metagenomics (https://www.ebi.ac.uk/metagenomics/) is a freely available hub for the analysis and archiving of metagenomic and metatranscriptomic data. Over the last 2 years, the resource has undergone rapid growth, with an increase of over five-fold in the number of processed samples and consequently represents one of the largest resources of analysed shotgun metagenomes. Here, we report the status of the resource in 2016 and give an overview of new developments. In particular, we describe updates to data content, a complete overhaul of the analysis pipeline, streamlining of data presentation via the website and the development of a new web based tool to compare functional analyses of sequence runs within a study. We also highlight two of the higher profile projects that have been analysed using the resource in the last year: the oceanographic projects Ocean Sampling Day and Tara Oceans.


Standards in Genomic Sciences | 2010

Meeting Report from the Second “Minimum Information for Biological and Biomedical Investigations” (MIBBI) workshop

Carsten Kettner; Dawn Field; Susanna-Assunta Sansone; Chris F. Taylor; Jan Aerts; Nigel Binns; Andrew Blake; Cedrik M. Britten; Ario de Marco; Jennifer Fostel; Pascale Gaudet; Alejandra Gonzalez-Beltran; Nigel Hardy; Jan Hellemans; Henning Hermjakob; Nick Juty; Jim Leebens-Mack; Eamonn Maguire; Steffen Neumann; Sandra Orchard; Helen Parkinson; William H. Piel; Shoba Ranganathan; Philippe Rocca-Serra; Annapaola Santarsiero; David M. Shotton; Peter Sterk; Andreas Untergasser; Patricia L. Whetzel

This report summarizes the proceedings of the second workshop of the ‘Minimum Information for Biological and Biomedical Investigations’ (MIBBI) consortium held on Dec 1–2, 2010 in Rüdesheim, Germany through the sponsorship of the Beilstein-Institute. MIBBI is an umbrella organization uniting communities developing Minimum Information (MI) checklists to standardize the description of data sets, the workflows by which they were generated and the scientific context for the work. This workshop brought together representatives of more than twenty communities to present the status of their MI checklists and plans for future development. Shared challenges and solutions were identified and the role of MIBBI in MI checklist development was discussed. The meeting featured some thirty presentations, wide-ranging discussions and breakout groups. The top outcomes of the two-day workshop as defined by the participants were: 1) the chance to share best practices and to identify areas of synergy; 2) defining a series of tasks for updating the MIBBI Portal; 3) reemphasizing the need to maintain independent MI checklists for various communities while leveraging common terms and workflow elements contained in multiple checklists; and 4) revision of the concept of the MIBBI Foundry to focus on the creation of a core set of MIBBI modules intended for reuse by individual MI checklist projects while maintaining the integrity of each MI project. Further information about MIBBI and its range of activities can be found at http://mibbi.org/.


Standards in Genomic Sciences | 2010

Meeting Report: BioSharing at ISMB 2010

Dawn Field; Susanna Sansone; Edward F. DeLong; Peter Sterk; Iddo Friedberg; Pascale Gaudet; Susanna Lewis; Renzo Kottmann; Lynette Hirschman; George M Garrity; Guy Cochrane; John Wooley; Folker Meyer; Sarah Hunter; Owen White; Brian Bramlett; Susan K. Gregurick; Hilmar Lapp; Sandra Orchard; Philippe Rocca-Serra; Alan Ruttenberg; Nigam H. Shah; Chris F. Taylor; Anne E. Thessen

This report summarizes the proceedings of the one day BioSharing meeting held at the Intelligent Systems for Molecular Biology (ISMB) 2010 conference in Boston, MA, USA This inaugural BioSharing event was hosted by the Genomic Standards Consortium as part of its M3 & BioSharing special interest group (SIG) workshop. The BioSharing event included invited talks from a range of community leaders and a panel discussion at the end of the day. The panel session led to the formal agreement among community leaders to join together to promote cross-community knowledge exchange and collaborations. A key focus of the newly formed Biosharing community will be linking up resources to promote real-world data sharing (virtuous cycle of data) and supporting compliance with data policies through the creation of a one-stop-portal of information. Further information about the newly established BioSharing effort can be found at http://biosharing.org.


Comparative and Functional Genomics | 2005

eGenomics: Cataloguing Our Complete Genome Collection III

Dawn Field; George M Garrity; Tanya Gray; Jeremy D. Selengut; Peter Sterk; Nicholas R. Thomson; Tatiana Tatusova; Guy Cochrane; Frank Oliver Glöckner; Renzo Kottmann; Allyson L. Lister; Yoshio Tateno; Robert Vaughan

This meeting report summarizes the proceedings of the “eGenomics: Cataloguing our Complete Genome Collection III” workshop held September 11–13, 2006, at the National Institute for Environmental eScience (NIEeS), Cambridge, United Kingdom. This 3rd workshop of the Genomic Standards Consortium was divided into two parts. The first half of the three-day workshop was dedicated to reviewing the genomic diversity of our current and future genome and metagenome collection, and exploring linkages to a series of existing projects through formal presentations. The second half was dedicated to strategic discussions. Outcomes of the workshop include a revised “Minimum Information about a Genome Sequence” (MIGS) specification (v1.1), consensus on a variety of features to be added to the Genome Catalogue (GCat), agreement by several researchers to adopt MIGS for imminent genome publications, and an agreement by the EBI and NCBI to input their genome collections into GCat for the purpose of quantifying the amount of optional data already available (e.g., for geographic location coordinates) and working towards a single, global list of all public genomes and metagenomes.


Standards in Genomic Sciences | 2014

Genomic Standards Consortium Projects

Dawn Field; Peter Sterk; Renzo Kottmann; J. Wim De Smet; Linda A. Amaral-Zettler; Guy Cochrane; James R. Cole; Neil Davies; Peter Dawyndt; George M Garrity; Jack A. Gilbert; Frank Oliver Glöckner; Lynette Hirschman; Hans-Peter Klenk; Rob Knight; Nikos C. Kyrpides; Folker Meyer; Ilene Karsch-Mizrachi; Norman Morrison; Robert J. Robbins; Inigo San Gil; Susanna Sansone; Lynn M. Schriml; Tatiana Tatusova; Dave Ussery; Pelin Yilmaz; Owen White; John Wooley; Gregory Caporaso

The Genomic Standards Consortium (GSC) is an open-membership community that was founded in 2005 to work towards the development, implementation and harmonization of standards in the field of genomics. Starting with the defined task of establishing a minimal set of descriptions the GSC has evolved into an active standards-setting body that currently has 18 ongoing projects, with additional projects regularly proposed from within and outside the GSC. Here we describe our recently enacted policy for proposing new activities that are intended to be taken on by the GSC, along with the template for proposing such new activities.


Viruses | 2010

Towards Viral Genome Annotation Standards, Report from the 2010 NCBI Annotation Workshop

James Rodney Brister; Yiming Bao; Carla Kuiken; Elliot J. Lefkowitz; Philippe Le Mercier; Raphael Leplae; Ramana Madupu; Richard H. Scheuermann; Seth Schobel; Donald Seto; Susmita Shrivastava; Peter Sterk; Qiandong Zeng; William Klimke; Tatiana Tatusova

Improvements in DNA sequencing technologies portend a new era in virology and could possibly lead to a giant leap in our understanding of viral evolution and ecology. Yet, as viral genome sequences begin to fill the world’s biological databases, it is critically important to recognize that the scientific promise of this era is dependent on consistent and comprehensive genome annotation. With this in mind, the NCBI Genome Annotation Workshop recently hosted a study group tasked with developing sequence, function, and metadata annotation standards for viral genomes. This report describes the issues involved in viral genome annotation and reviews policy recommendations presented at the NCBI Annotation Workshop.

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Guy Cochrane

European Bioinformatics Institute

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Nikos C. Kyrpides

European Bioinformatics Institute

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Tatiana Tatusova

National Institutes of Health

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