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Featured researches published by Martin Hammond.


Nucleic Acids Research | 2002

The Ensembl genome database project

Tim Hubbard; Darren Barker; Ewan Birney; Graham Cameron; Yuan Chen; L. Clark; Tony Cox; James Cuff; V. Curwen; Thomas A. Down; Richard Durbin; E. Eyras; James Gilbert; Martin Hammond; L. Huminiecki; Arek Kasprzyk; Heikki Lehväslaiho; Philip Lijnzaad; Craig Melsopp; Emmanuel Mongin; R. Pettett; M. Pocock; Simon Potter; A. Rust; Esther Schmidt; Stephen M. J. Searle; Guy Slater; J. Smith; W. Spooner; A. Stabenau

The Ensembl (http://www.ensembl.org/) database project provides a bioinformatics framework to organise biology around the sequences of large genomes. It is a comprehensive source of stable automatic annotation of the human genome sequence, with confirmed gene predictions that have been integrated with external data sources, and is available as either an interactive web site or as flat files. It is also an open source software engineering project to develop a portable system able to handle very large genomes and associated requirements from sequence analysis to data storage and visualisation. The Ensembl site is one of the leading sources of human genome sequence annotation and provided much of the analysis for publication by the international human genome project of the draft genome. The Ensembl system is being installed around the world in both companies and academic sites on machines ranging from supercomputers to laptops.


Science | 2007

Genome sequence of Aedes aegypti, a major arbovirus vector

Vishvanath Nene; Jennifer R. Wortman; Daniel John Lawson; Brian J. Haas; Chinnappa D. Kodira; Zhijian Jake Tu; Brendan J. Loftus; Zhiyong Xi; Karyn Megy; Manfred Grabherr; Quinghu Ren; Evgeny M. Zdobnov; Neil F. Lobo; Kathryn S. Campbell; Susan E. Brown; Maria F. Bonaldo; Jingsong Zhu; Steven P. Sinkins; David G. Hogenkamp; Paolo Amedeo; Peter Arensburger; Peter W. Atkinson; Shelby Bidwell; Jim Biedler; Ewan Birney; Robert V. Bruggner; Javier Costas; Monique R. Coy; Jonathan Crabtree; Matt Crawford

We present a draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and dengue fever, which at ∼1376 million base pairs is about 5 times the size of the genome of the malaria vector Anopheles gambiae. Nearly 50% of the Ae. aegypti genome consists of transposable elements. These contribute to a factor of ∼4 to 6 increase in average gene length and in sizes of intergenic regions relative to An. gambiae and Drosophila melanogaster. Nonetheless, chromosomal synteny is generally maintained among all three insects, although conservation of orthologous gene order is higher (by a factor of ∼2) between the mosquito species than between either of them and the fruit fly. An increase in genes encoding odorant binding, cytochrome P450, and cuticle domains relative to An. gambiae suggests that members of these protein families underpin some of the biological differences between the two mosquito species.


Science | 2010

Sequencing of Culex quinquefasciatus establishes a platform for mosquito comparative genomics.

Peter Arensburger; Karine Megy; Robert M. Waterhouse; Jenica Abrudan; Paolo Amedeo; Beatriz García Antelo; Lyric C. Bartholomay; Shelby Bidwell; Elisabet Caler; Francisco Camara; Corey L. Campbell; Kathryn S. Campbell; Claudio Casola; Marta T. Castro; Ishwar Chandramouliswaran; Sinéad B. Chapman; Scott Christley; Javier Costas; Eric Eisenstadt; Cédric Feschotte; Claire M. Fraser-Liggett; Roderic Guigó; Brian J. Haas; Martin Hammond; Bill S. Hansson; Janet Hemingway; Sharon R. Hill; Clint Howarth; Rickard Ignell; Ryan C. Kennedy

Closing the Vector Circle The genome sequence of Culex quinquefasciatus offers a representative of the third major genus of mosquito disease vectors for comparative analysis. In a major international effort, Arensburger et al. (p. 86) uncovered divergences in the C. quinquefasciatus genome compared with the representatives of the other two genera Aedes aegypti and Anopheles gambiae. The main difference noted is the expansion of numbers of genes, particularly for immunity, oxidoreductive functions, and digestive enzymes, which may reflect specific aspects of the Culex life cycle. Bartholomay et al. (p. 88) explored infection-response genes in Culex in more depth and uncovered 500 immune response-related genes, similar to the numbers seen in Aedes, but fewer than seen in Anopheles or the fruit fly Drosophila melanogaster. The higher numbers of genes were attributed partly to expansions in those encoding serpins, C-type lectins, and fibrinogen-related proteins, consistent with greater immune surveillance and associated signaling needed to monitor the dangers of breeding in polluted, urbanized environments. Transcriptome analysis confirmed that inoculation with unfamiliar bacteria prompted strong immune responses in Culex. The worm and virus pathogens that the mosquitoes transmit naturally provoked little immune activation, however, suggesting that tolerance has evolved to any damage caused by replication of the pathogens in the insects. The genome of a third mosquito species reveals distinctions related to vector capacities and habitat preferences. Culex quinquefasciatus (the southern house mosquito) is an important mosquito vector of viruses such as West Nile virus and St. Louis encephalitis virus, as well as of nematodes that cause lymphatic filariasis. C. quinquefasciatus is one species within the Culex pipiens species complex and can be found throughout tropical and temperate climates of the world. The ability of C. quinquefasciatus to take blood meals from birds, livestock, and humans contributes to its ability to vector pathogens between species. Here, we describe the genomic sequence of C. quinquefasciatus: Its repertoire of 18,883 protein-coding genes is 22% larger than that of Aedes aegypti and 52% larger than that of Anopheles gambiae with multiple gene-family expansions, including olfactory and gustatory receptors, salivary gland genes, and genes associated with xenobiotic detoxification.


Nucleic Acids Research | 2010

Ensembl’s 10th year

Paul Flicek; Bronwen Aken; Benoit Ballester; Kathryn Beal; Eugene Bragin; Simon Brent; Yuan Chen; Peter Clapham; Guy Coates; Susan Fairley; Stephen Fitzgerald; Julio Fernandez-Banet; Leo Gordon; Stefan Gräf; Syed Haider; Martin Hammond; Kerstin Howe; Andrew M. Jenkinson; Nathan Johnson; Andreas Kähäri; Damian Keefe; Stephen Keenan; Rhoda Kinsella; Felix Kokocinski; Gautier Koscielny; Eugene Kulesha; Daniel Lawson; Ian Longden; Tim Massingham; William M. McLaren

Ensembl (http://www.ensembl.org) integrates genomic information for a comprehensive set of chordate genomes with a particular focus on resources for human, mouse, rat, zebrafish and other high-value sequenced genomes. We provide complete gene annotations for all supported species in addition to specific resources that target genome variation, function and evolution. Ensembl data is accessible in a variety of formats including via our genome browser, API and BioMart. This year marks the tenth anniversary of Ensembl and in that time the project has grown with advances in genome technology. As of release 56 (September 2009), Ensembl supports 51 species including marmoset, pig, zebra finch, lizard, gorilla and wallaby, which were added in the past year. Major additions and improvements to Ensembl since our previous report include the incorporation of the human GRCh37 assembly, enhanced visualisation and data-mining options for the Ensembl regulatory features and continued development of our software infrastructure.


Nucleic Acids Research | 2003

Ensembl 2002: accommodating comparative genomics

Michele Clamp; D. Andrews; Darren Barker; Paul Bevan; Graham Cameron; Yuting Chen; Louise Clark; Tony Cox; James Cuff; Val Curwen; Thomas A. Down; Richard Durbin; Eduardo Eyras; James Gilbert; Martin Hammond; Tim Hubbard; Arek Kasprzyk; Damian Keefe; Heikki Lehväslaiho; Vishwanath R. Iyer; Craig Melsopp; Emmanuel Mongin; Roger Pettett; Simon Potter; Alistair G. Rust; Esther Schmidt; Steve Searle; Guy Slater; James Smith; William Spooner

The Ensembl (http://www.ensembl.org/) database project provides a bioinformatics framework to organise biology around the sequences of large genomes. It is a comprehensive source of stable automatic annotation of human, mouse and other genome sequences, available as either an interactive web site or as flat files. Ensembl also integrates manually annotated gene structures from external sources where available. As well as being one of the leading sources of genome annotation, Ensembl is an open source software engineering project to develop a portable system able to handle very large genomes and associated requirements. These range from sequence analysis to data storage and visualisation and installations exist around the world in both companies and at academic sites. With both human and mouse genome sequences available and more vertebrate sequences to follow, many of the recent developments in Ensembl have focusing on developing automatic comparative genome analysis and visualisation.


Nucleic Acids Research | 2009

VectorBase: A Data Resource for Invertebrate Vector Genomics

Daniel John Lawson; Peter Arensburger; Peter W. Atkinson; Nora J. Besansky; Robert V. Bruggner; Ryan Butler; Kathryn S. Campbell; George K. Christophides; Scott Christley; Emmanuel Dialynas; Martin Hammond; Catherine A. Hill; Nathan Konopinski; Neil F. Lobo; Robert M. MacCallum; Gregory R. Madey; Karine Megy; Jason M. Meyer; Seth Redmond; David W. Severson; Eric O. Stinson; Pantelis Topalis; Ewan Birney; William M. Gelbart; Fotis C. Kafatos; Christos Louis; Frank H. Collins

VectorBase (http://www.vectorbase.org) is an NIAID-funded Bioinformatic Resource Center focused on invertebrate vectors of human pathogens. VectorBase annotates and curates vector genomes providing a web accessible integrated resource for the research community. Currently, VectorBase contains genome information for three mosquito species: Aedes aegypti, Anopheles gambiae and Culex quinquefasciatus, a body louse Pediculus humanus and a tick species Ixodes scapularis. Since our last report VectorBase has initiated a community annotation system, a microarray and gene expression repository and controlled vocabularies for anatomy and insecticide resistance. We have continued to develop both the software infrastructure and tools for interrogating the stored data.


Nucleic Acids Research | 2007

VectorBase: a home for invertebrate vectors of human pathogens

Daniel John Lawson; Peter Arensburger; Peter W. Atkinson; Nora J. Besansky; Robert V. Bruggner; Ryan Butler; Kathryn S. Campbell; George K. Christophides; Scott Christley; Emmanuel Dialynas; David B. Emmert; Martin Hammond; Catherine A. Hill; Ryan C. Kennedy; Neil F. Lobo; Robert M. MacCallum; Gregory R. Madey; Karine Megy; Seth Redmond; Susan Russo; David W. Severson; Eric O. Stinson; Pantelis Topalis; Evgeni M. Zdobnov; Ewan Birney; William M. Gelbart; Fotis C. Kafatos; Christos Louis; Frank H. Collins

VectorBase () is a web-accessible data repository for information about invertebrate vectors of human pathogens. VectorBase annotates and maintains vector genomes providing an integrated resource for the research community. Currently, VectorBase contains genome information for two organisms: Anopheles gambiae, a vector for the Plasmodium protozoan agent causing malaria, and Aedes aegypti, a vector for the flaviviral agents causing Yellow fever and Dengue fever.


Genome Biology | 2007

Update of the Anopheles gambiae PEST genome assembly

Maria V. Sharakhova; Martin Hammond; Neil F. Lobo; Jaroslaw Krzywinski; Maria F. Unger; Maureen E. Hillenmeyer; Robert V. Bruggner; Ewan Birney; Frank H. Collins

BackgroundThe genome of Anopheles gambiae, the major vector of malaria, was sequenced and assembled in 2002. This initial genome assembly and analysis made available to the scientific community was complicated by the presence of assembly issues, such as scaffolds with no chromosomal location, no sequence data for the Y chromosome, haplotype polymorphisms resulting in two different genome assemblies in limited regions and contaminating bacterial DNA.ResultsPolytene chromosome in situ hybridization with cDNA clones was used to place 15 unmapped scaffolds (sizes totaling 5.34 Mbp) in the pericentromeric regions of the chromosomes and oriented a further 9 scaffolds. Additional analysis by in situ hybridization of bacterial artificial chromosome (BAC) clones placed 1.32 Mbp (5 scaffolds) in the physical gaps between scaffolds on euchromatic parts of the chromosomes. The Y chromosome sequence information (0.18 Mbp) remains highly incomplete and fragmented among 55 short scaffolds. Analysis of BAC end sequences showed that 22 inter-scaffold gaps were spanned by BAC clones. Unmapped scaffolds were also aligned to the chromosome assemblies in silico, identifying regions totaling 8.18 Mbp (144 scaffolds) that are probably represented in the genome project by two alternative assemblies. An additional 3.53 Mbp of alternative assembly was identified within mapped scaffolds. Scaffolds comprising 1.97 Mbp (679 small scaffolds) were identified as probably derived from contaminating bacterial DNA. In total, about 33% of previously unmapped sequences were placed on the chromosomes.ConclusionThis study has used new approaches to improve the physical map and assembly of the A. gambiae genome.


Infection, Genetics and Evolution | 2009

Genomic Resources for Invertebrate Vectors of Human Pathogens, and the role of VectorBase

Karyn Megy; Martin Hammond; Daniel Lawson; Robert V. Bruggner; Ewan Birney; Frank H. Collins

High-throughput genome sequencing techniques have now reached vector biology with an emphasis on those species that are vectors of human pathogens. The first mosquito to be sequenced was Anopheles gambiae, the vector for Plasmodium parasites that cause malaria. Further mosquitoes have followed: Aedes aegypti (yellow fever and dengue fever vector) and Culex pipiens (lymphatic filariasis and West Nile fever). Species that are currently in sequencing include the body louse Pediculus humanus (Typhus vector), the triatomine Rhodnius prolixus (Chagas disease vector) and the tick Ixodes scapularis (Lyme disease vector). The motivations for sequencing vector genomes are to further understand vector biology, with an eye on developing new control strategies (for example novel chemical attractants or repellents) or understanding the limitations of current strategies (for example the mechanism of insecticide resistance); to analyse the mechanisms driving their evolution; and to perform an exhaustive analysis of the gene repertory. The proliferation of genomic data creates the need for efficient and accessible storage. We present VectorBase, a genomic resource centre that is both involved in the annotation of vector genomes and act as a portal for access to the genomic information (http://www.vectorbase.org).


Genome Research | 2003

EnsMart: A Generic System for Fast and Flexible Access to Biological Data

Arek Kasprzyk; Damian Keefe; Damian Smedley; Darin London; William Spooner; Craig Melsopp; Martin Hammond; Philippe Rocca-Serra; Tony Cox; Ewan Birney

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Ewan Birney

European Bioinformatics Institute

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Neil F. Lobo

University of Notre Dame

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Craig Melsopp

European Bioinformatics Institute

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Damian Keefe

European Bioinformatics Institute

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Karine Megy

European Bioinformatics Institute

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Shelby Bidwell

J. Craig Venter Institute

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