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Dive into the research topics where Yasmin Alam-Faruque is active.

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Featured researches published by Yasmin Alam-Faruque.


Nucleic Acids Research | 2007

IntAct—open source resource for molecular interaction data

Samuel Kerrien; Yasmin Alam-Faruque; Bruno Aranda; I. Bancarz; Alan Bridge; C. Derow; Emily Dimmer; Marc Feuermann; A. Friedrichsen; Rachael P. Huntley; C. Kohler; Jyoti Khadake; Catherine Leroy; A. Liban; C. Lieftink; Luisa Montecchi-Palazzi; Sandra Orchard; Judith E. Risse; Karine Robbe; Bernd Roechert; David Thorneycroft; Y. Zhang; Rolf Apweiler; Henning Hermjakob

IntAct is an open source database and software suite for modeling, storing and analyzing molecular interaction data. The data available in the database originates entirely from published literature and is manually annotated by expert biologists to a high level of detail, including experimental methods, conditions and interacting domains. The database features over 126 000 binary interactions extracted from over 2100 scientific publications and makes extensive use of controlled vocabularies. The web site provides tools allowing users to search, visualize and download data from the repository. IntAct supports and encourages local installations as well as direct data submission and curation collaborations. IntAct source code and data are freely available from .


Nucleic Acids Research | 2012

The UniProt-GO Annotation database in 2011

Emily Dimmer; Rachael P. Huntley; Yasmin Alam-Faruque; Tony Sawford; Claire O'Donovan; María Martín; Benoit Bely; Paul Browne; Wei Mun Chan; Ruth Eberhardt; Michael Gardner; Kati Laiho; D Legge; Michele Magrane; Klemens Pichler; Diego Poggioli; Harminder Sehra; Andrea H. Auchincloss; Kristian B. Axelsen; Marie-Claude Blatter; Emmanuel Boutet; Silvia Braconi-Quintaje; Lionel Breuza; Alan Bridge; Elizabeth Coudert; Anne Estreicher; L Famiglietti; Serenella Ferro-Rojas; Marc Feuermann; Arnaud Gos

The GO annotation dataset provided by the UniProt Consortium (GOA: http://www.ebi.ac.uk/GOA) is a comprehensive set of evidenced-based associations between terms from the Gene Ontology resource and UniProtKB proteins. Currently supplying over 100 million annotations to 11 million proteins in more than 360 000 taxa, this resource has increased 2-fold over the last 2 years and has benefited from a wealth of checks to improve annotation correctness and consistency as well as now supplying a greater information content enabled by GO Consortium annotation format developments. Detailed, manual GO annotations obtained from the curation of peer-reviewed papers are directly contributed by all UniProt curators and supplemented with manual and electronic annotations from 36 model organism and domain-focused scientific resources. The inclusion of high-quality, automatic annotation predictions ensures the UniProt GO annotation dataset supplies functional information to a wide range of proteins, including those from poorly characterized, non-model organism species. UniProt GO annotations are freely available in a range of formats accessible by both file downloads and web-based views. In addition, the introduction of a new, normalized file format in 2010 has made for easier handling of the complete UniProt-GOA data set.


BMC Bioinformatics | 2014

A method for increasing expressivity of Gene Ontology annotations using a compositional approach

Rachael P. Huntley; Midori A. Harris; Yasmin Alam-Faruque; Judith A. Blake; Seth Carbon; Heiko Dietze; Emily Dimmer; Rebecca E. Foulger; David P. Hill; Varsha K. Khodiyar; Antonia Lock; Jane Lomax; Ruth C. Lovering; Prudence Mutowo-Meullenet; Tony Sawford; Kimberly Van Auken; Valerie Wood; Christopher J. Mungall

BackgroundThe Gene Ontology project integrates data about the function of gene products across a diverse range of organisms, allowing the transfer of knowledge from model organisms to humans, and enabling computational analyses for interpretation of high-throughput experimental and clinical data. The core data structure is the annotation, an association between a gene product and a term from one of the three ontologies comprising the GO. Historically, it has not been possible to provide additional information about the context of a GO term, such as the target gene or the location of a molecular function. This has limited the specificity of knowledge that can be expressed by GO annotations.ResultsThe GO Consortium has introduced annotation extensions that enable manually curated GO annotations to capture additional contextual details. Extensions represent effector–target relationships such as localization dependencies, substrates of protein modifiers and regulation targets of signaling pathways and transcription factors as well as spatial and temporal aspects of processes such as cell or tissue type or developmental stage. We describe the content and structure of annotation extensions, provide examples, and summarize the current usage of annotation extensions.ConclusionsThe additional contextual information captured by annotation extensions improves the utility of functional annotation by representing dependencies between annotations to terms in the different ontologies of GO, external ontologies, or an organism’s gene products. These enhanced annotations can also support sophisticated queries and reasoning, and will provide curated, directional links between many gene products to support pathway and network reconstruction.


PLOS ONE | 2011

The Impact of Focused Gene Ontology Curation of Specific Mammalian Systems

Yasmin Alam-Faruque; Rachael P. Huntley; Varsha K. Khodiyar; Evelyn Camon; Emily Dimmer; Tony Sawford; María Martín; Claire O'Donovan; Philippa J. Talmud; Peter J. Scambler; Rolf Apweiler; Ruth C. Lovering

The Gene Ontology (GO) resource provides dynamic controlled vocabularies to provide an information-rich resource to aid in the consistent description of the functional attributes and subcellular locations of gene products from all taxonomic groups (www.geneontology.org). System-focused projects, such as the Renal and Cardiovascular GO Annotation Initiatives, aim to provide detailed GO data for proteins implicated in specific organ development and function. Such projects support the rapid evaluation of new experimental data and aid in the generation of novel biological insights to help alleviate human disease. This paper describes the improvement of GO data for renal and cardiovascular research communities and demonstrates that the cardiovascular-focused GO annotations, created over the past three years, have led to an evident improvement of microarray interpretation. The reanalysis of cardiovascular microarray datasets confirms the need to continue to improve the annotation of the human proteome. Availability GO annotation data is freely available from: ftp://ftp.geneontology.org/pub/go/gene-associations/


Database | 2013

Use of Gene Ontology Annotation to understand the peroxisome proteome in humans

Prudence Mutowo-Meullenet; Rachael P. Huntley; Emily Dimmer; Yasmin Alam-Faruque; Tony Sawford; María Martín; Claire O’Donovan; Rolf Apweiler

The Gene Ontology (GO) is the de facto standard for the functional description of gene products, providing a consistent, information-rich terminology applicable across species and information repositories. The UniProt Consortium uses both manual and automatic GO annotation approaches to curate UniProt Knowledgebase (UniProtKB) entries. The selection of a protein set prioritized for manual annotation has implications for the characteristics of the information provided to users working in a specific field or interested in particular pathways or processes. In this article, we describe an organelle-focused, manual curation initiative targeting proteins from the human peroxisome. We discuss the steps taken to define the peroxisome proteome and the challenges encountered in defining the boundaries of this protein set. We illustrate with the use of examples how GO annotations now capture cell and tissue type information and the advantages that such an annotation approach provides to users. Database URL: http://www.ebi.ac.uk/GOA/ and http://www.uniprot.org


PLOS ONE | 2014

Representing kidney development using the gene ontology.

Yasmin Alam-Faruque; David P. Hill; Emily Dimmer; Midori A. Harris; Rebecca E. Foulger; Susan Tweedie; Helen Attrill; Douglas G. Howe; Stephen Randall Thomas; Duncan Davidson; Adrian S. Woolf; Judith A. Blake; Christopher J. Mungall; Claire O’Donovan; Rolf Apweiler; Rachael P. Huntley

Gene Ontology (GO) provides dynamic controlled vocabularies to aid in the description of the functional biological attributes and subcellular locations of gene products from all taxonomic groups (www.geneontology.org). Here we describe collaboration between the renal biomedical research community and the GO Consortium to improve the quality and quantity of GO terms describing renal development. In the associated annotation activity, the new and revised terms were associated with gene products involved in renal development and function. This project resulted in a total of 522 GO terms being added to the ontology and the creation of approximately 9,600 kidney-related GO term associations to 940 UniProt Knowledgebase (UniProtKB) entries, covering 66 taxonomic groups. We demonstrate the impact of these improvements on the interpretation of GO term analyses performed on genes differentially expressed in kidney glomeruli affected by diabetic nephropathy. In summary, we have produced a resource that can be utilized in the interpretation of data from small- and large-scale experiments investigating molecular mechanisms of kidney function and development and thereby help towards alleviating renal disease.


Organogenesis | 2010

The Renal Gene Ontology Annotation Initiative

Yasmin Alam-Faruque; Emily Dimmer; Rachael P. Huntley; Claire O'Donovan; Peter J. Scambler; Rolf Apweiler

The Gene Ontology (GO) resource provides dynamic controlled vocabularies to aid in the description of the functional attributes and subcellular locations of gene products from all taxonomic groups (www.geneontology.org). A renal-focused curation initiative, funded by Kidney Research UK and supported by the GO Consortium, has started at the European Bioinformatics Institute and aims to provide a detailed GO resource for mammalian proteins implicated in renal development and function. This report outlines the aims of this initiative and explains how the renal community can become involved to help improve the availability, quality and quantity of GO terms and their association to specific proteins.

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Emily Dimmer

European Bioinformatics Institute

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Rachael P. Huntley

European Bioinformatics Institute

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Rolf Apweiler

European Bioinformatics Institute

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Tony Sawford

European Bioinformatics Institute

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Claire O'Donovan

European Bioinformatics Institute

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María Martín

European Bioinformatics Institute

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Claire O’Donovan

European Bioinformatics Institute

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Prudence Mutowo-Meullenet

European Bioinformatics Institute

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