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1.
Genetics ; 200(3): 675-8, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26170440

RESUMO

The Genetics Society of America's George W. Beadle Award honors individuals who have made outstanding contributions to the community of genetics researchers and who exemplify the qualities of its namesake as a respected academic, administrator, and public servant. The 2015 recipient is John Postlethwait. He has made groundbreaking contributions in developing the zebrafish as a molecular genetic model and in understanding the evolution of new gene functions in vertebrates. He built the first zebrafish genetic map and showed that its genome, along with that of distantly related teleost fish, had been duplicated. Postlethwait played an integral role in the zebrafish genome-sequencing project and elucidated the genomic organization of several fish species. Postlethwait is also honored for his active involvement with the zebrafish community, advocacy for zebrafish as a model system, and commitment to driving the field forward.


Assuntos
Distinções e Prêmios , Genética/história , Animais , Variação Genética , História do Século XX , História do Século XXI , Mapeamento Físico do Cromossomo/história , Seleção Genética , Análise de Sequência de DNA/história , Sociedades Científicas , Estados Unidos , Peixe-Zebra/genética
3.
BMC Genet ; 6 Suppl 1: S63, 2005 Dec 30.
Artigo em Inglês | MEDLINE | ID: mdl-16451676

RESUMO

BACKGROUND: There is great interest in the use of computationally intensive methods for fine mapping of marker data. In this paper we develop methods based upon ideas originally proposed 100 years ago in the context of spatial clustering. METHODS: We use spatial clustering of haplotypes as a low-dimensional surrogate for the unobserved genealogy underlying a set of genotype data. In doing so we hope to avoid the computational complexity inherent in explicitly modelling details of the ancestry of the sample, while at the same time capturing the key correlations induced by that ancestry at a much lower computational cost. RESULTS: We benchmark our methods using the simulated Genetic Analysis Workshop 14 data, using 100 replicates of 4 phenotypes to indicate the power of our method. When a functional mutation relating to a trait is actually present, we find evidence for that mutation in 97 out of 100 replicates, on average. CONCLUSION: Our results show that our method has the ability to accurately infer the location of functional mutations from unphased genotype data.


Assuntos
Mapeamento Físico do Cromossomo/história , Congressos como Assunto , História do Século XX , Humanos , Mutação/genética , Fenótipo , Reprodutibilidade dos Testes
5.
Pharmacogenomics ; 2(1): 37-49, 2001 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11258196

RESUMO

Efforts in genomics over the last decade have created a stream of opportunities for drug discovery. High-throughput DNA sequencing has forced a re-definition of the paradigm for identification and validation of targets for drug development. One purpose of this review is to delineate the different approaches to sequence data generation and to establish their various uses for the definition of gene function. There still remain crucial dilemmas for the pharmaceutical industry. The multitude of potential targets can each absorb enormous validation costs and the vast majority are likely to prove academically interesting but useless for drug development. An additional dimension arises from the importance of sequence variation between different individuals. These differences can determine response to therapy and must inform both the drug development process and healthcare delivery. This presents great challenges and opportunities for drug companies, their customers and society as a whole. I will review the technological aspects in some detail and give my view of the legal and social aspects. The field of bioinformatics is at the core of functional and pharmacogenomics and advances will depend on the continuing evolution of tools to interpret data. For the most part this evolution is reviewed in the context of specific application areas rather than as a discrete field, in recognition of its all-pervasive effects.


Assuntos
Mapeamento Cromossômico/história , Projeto Genoma Humano/história , Animais , Mapeamento Cromossômico/métodos , Etiquetas de Sequências Expressas , História do Século XX , Humanos , Mapeamento Físico do Cromossomo/história , Polimorfismo de Nucleotídeo Único
6.
Science ; 287(5461): 2216-8, 2000 Mar 24.
Artigo em Inglês | MEDLINE | ID: mdl-10731135

RESUMO

The sequence of the Drosophila melanogaster genome presented in this issue of Science is the latest milestone in nine decades of research on this organism. Genetic and physical mapping, whole-genome mutational screens, and functional alteration of the genome by gene transfer were pioneered in metazoans with the use of this small fruit fly. Here we look at some of the instances in which work on Drosophila has led to major conceptual or technical breakthroughs in our understanding of animal genomes.


Assuntos
Drosophila melanogaster/genética , Genética/história , Genoma , Animais , Animais Geneticamente Modificados , Mapeamento Cromossômico/história , Clonagem Molecular , Biologia Computacional/história , Genes de Insetos , História do Século XX , Mutação , Prêmio Nobel , Mapeamento Físico do Cromossomo/história , Recombinação Genética , Análise de Sequência de DNA
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