| |
|
|
| Registros recuperados : 38 | |
| 2. |  | BARBIERI, F. S.; BRITO, L. G.; BARROS-BATTESTI, D.; LABRUNA, M. B.; CAMARGO, L. M. A. Descrição morfológica da larva de Amblyomma pacae Aragão, 1911 (ACARI: IXODIDAE) através de microscopia óptica e eletrônica de varredura. In: CONGRESSO BRASILEIRO DE PARASIOTOLOGIA VETERINÁRIA, 14.; SIMPOSIO LATINO-AMERICANO DE RICKETTSIOSES, 2., 2006, Ribeirão Preto. Programa e resumos. Ribeirão Preto: CBPV, 2006. v. 1. p. 205.| Biblioteca(s): Embrapa Rondônia. |
|    |
| 4. | | ALMEIDA, R. F. C; ANDREOTTI, R.; LABRUNA, M. B; MATOS, M. F. C. Ocorrência de anticorpos anti- rickettsia spp em equinos de Mato Grosso do Sul In: CONGRESSO BRASILEIRO DE PARASITOLOGIA VETERINÁRIA, 16., 2010, Campo Grande, MS. [Anais...]. Campo Grande, MS: Colégio Brasileiro de Parasitologia Veterinária, 2010. 1 CD-ROM. 1 p.| Biblioteca(s): Embrapa Gado de Corte. |
| |
| 7. | | TERASSINI, F. A.; BARBIERI, F. da S.; ALBUQUERQUE, S.; SZABÓ, M. P. J.; CAMARGO, L. M. A.; LABRUNA, M. B. Comparison of two methods for collecting free-living ticks in the Amazonian forest. Ticks and Tick-borne Diseases, v. 1, n. 4, p. 194-196, dec. 2010.| Biblioteca(s): Embrapa Rondônia. |
|  |
| 8. | | COSTA, F. B.; BARBERI, A. R. M.; SZABÓ, M. P. J.; RAMOS, V. N.; PIOVEZAN, U.; LABRUNA, M. B. New records of Rickettsia bellii-infected ticks in Brazil. Brazilian Journal of Veterinary Research and Animal Science, São Paulo, v. 54, n. 1, p. 92-95, 2017.| Biblioteca(s): Embrapa Pantanal. |
| |
| 9. | | LABRUNA, M. B.; BARBIERI, F. da S.; MARTINS, T. F.; BRITO, L. G.; RIBEIRO, F. D. S. New tick records in Rondônia, Wester brazilian Amazon. Separata de: Revista Brasileira de Parasitologia Veterinária, v. 19, n. 3, p. 192-194, jul./set. 2010.| Biblioteca(s): Embrapa Rondônia. |
| |
| 10. | | BARBIERI, F. S.; BRITO, L. G.; LABRUNA, M. B.; BARROS-BATTESTI, D. M.; CAMARGO, L. M. A.; FAMADAS, K. M. Description of the larva of Amblyoma ovale Koch, 1844 (Acari: Ixodidae) by light and scanning electron microscopy. Systematic and Applied Acarology, v. 13, p. 109-119, 2008. Meta 2008.| Biblioteca(s): Embrapa Rondônia. |
| |
| 11. | | BARBIERI, F. S.; BRITO, L. G.; LABRUNA, M. B.; BARROS-BATTESTI, D. M.; CAMARGO, L. M. A.; FAMADAS, K. M. Description of the larva of Amblyomma pacae Aragão, 1911 (Acari: Ixodidae) by light and scanning electron microscopy. Systematic and Applied Acarology, v. 13, p. 195-203, 2008. Metas 2008.| Biblioteca(s): Embrapa Rondônia. |
| |
| 12. | | OLIVEIRA, C. S.; BRAUNIG, P.; KRAWCZAK, F.; LABRUNA, M. B.; BOTTON, S. A.; VOGEL, F. S. F.; SANGIONI, L. A. Detecção de proteínas imunorreativas de Rickettsia sp. cepa Mata Atlântica. Pesquisa Veterinária Brasileira, Rio de Janeiro, v. 37, n. 1, p. 52-57, jan. 2017.| Biblioteca(s): Embrapa Unidades Centrais. |
| |
| 13. | | NIERI-BASTOS, F. A.; MARTINS, T. F.; CANCADO, P. H. D.; FACCINI, J. L. H.; LABRUNA, M. B. Detection of a spotted fever group rickettsia in Amblyomma parvum (Acari: Ixodidae) from the Pantanal biome, Brazil. Biomédica, v.31, p. 87-102, 2011. Supplement. Edição dos resumos do CONGRESSO LATINOAMERICANO DE ENFERMEDADES RICKETTSIALES, 3., ENCUENTRO NACIONAL DE FIEBRES HEMORRÁGICAS, 1., 2011, Bogotá. Presentaciones orales. Bogotá: Pontificia Universidad Javeriana, 2011. p. 94| Biblioteca(s): Embrapa Gado de Corte. |
| |
| 14. | | ALMEIDA, R. F. C.; GARCIA, M. V.; CUNHA, R. C.; MATIAS, J; LABRUNA, M. B.; ANDREOTTI, R. The first report of Rickettsia spp. in Amblyomma nodosum in the State of Mato Grosso do Sul, Brazil. Ticks and Tick Borne Diseases, v. 4, n.1-2, p. 156-159,Feb. 2013.| Biblioteca(s): Embrapa Gado de Corte. |
| |
| 15. | | PIRANDA, E. M.; FACCINI, J. L. H.; PINTER, A.; PACHECO, R. C.; CANCADO, P. H. D.; LABRUNA, M. B. Experimental infection of Rhipicephalus sanguineus ticks with the Bacterium Rickettsia rickettsii, using experimentally infected dogs. Vector-Borne and Zoonotic Diseases, v.11, n.1, p.29-36, 2011.| Biblioteca(s): Embrapa Gado de Corte. |
| |
| 16. | | ITO, F. H.; VASCONCELLOS, S. A.; BERNARDI, F.; NASCIMENTO, A. A.; LABRUNA, M. B.; ARANTES, I. G. Evidencia sorologica de brucelose e leptospirose e parasitismo por ixodideos em animais silvestres do Pantanal Sul-Mato-Grossense. Ars Veterinaria, Jaboticabal, v.14, n.3, p.302-310, dez., 1998.| Biblioteca(s): Embrapa Pantanal. |
| |
| 17. | | AGUIAR, D. M.; CAVALCANTE, G. T.; VASCONCELLOS, S. A.; SOUZA, G. O.; LABRUNA, M. B.; CAMARGO, L. M. A.; GENNARI, S. M. Anticorpos Anti-Leptospira spp. em ovinos do município de Monte Negro, Estado de Rondônia. Experimental and Toxicologic Pathology, v. 63, n. 3, p. 263-268, Mar. 2011.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
| |
| 18. | | PEREIRA, J. S.; MARTINS, T. F.; MUÑOZ-LEAL, S.; LOPES, M. G.; LABRUNA, M. B.; PAIVA, K. A. R. de; OLIVEIRA, M. F. de; AHID, S. M. M. Infestação por carrapatos Argasidae e Ixodidae em pequenos mamíferos silvestres da Estação Experimental Rafael Fernandes, Mossoró/RN. Pesquisa Veterinária Brasileira, Rio de Janeiro, v. 37, n. 7, p. 741-748,, julho 2017. Título em inglês: Infestation by ticks Argasidae and Ixodidae on small wild mammals at the Experimental Station Rafael Fernandes, Mossoró/RN, Brazil.| Biblioteca(s): Embrapa Unidades Centrais. |
| |
| 19. | | ARAUJO, A. C.; SILVEIRA, J. A. G.; AZEVEDO, S. S.; NIERI-BASTOS, F. A.; RIBEIRO, M. F. B.; LABRUNA, M. B.; HORTA, M. C. Babesia canis vogeli infection in dogs and ticks in the semiarid region of Pernanbuco, Brazil. Pesquisa Veterinária Brasileira, Rio de Janeiro v. 35, n. 5, p. 456-461, maio 2015.| Biblioteca(s): Embrapa Unidades Centrais. |
| |
| 20. | | BARBIERI, F. da S.; BRITO, L. G.; BATTESTI, D. M. B.; FAMADAS, K. M.; LABRUNA, M. B.; CAMARGO, L. M. A. Redescription of the larva of Amblyomma Obbongoguttatum Koch,1844(Acari:Ixodidae) by light and scanning electron microscopy. Zootaxa, New Zealand, v. 3579, nov. 2012.| Biblioteca(s): Embrapa Rondônia. |
| |
| Registros recuperados : 38 | |
|
|
|
Registro Completo
|
Biblioteca(s): |
Embrapa Agricultura Digital. |
|
Data corrente: |
06/12/2011 |
|
Data da última atualização: |
24/01/2020 |
|
Tipo da produção científica: |
Resumo em Anais de Congresso |
|
Autoria: |
CINTRA, L. C. |
|
Afiliação: |
LEANDRO CARRIJO CINTRA, CNPTIA. |
|
Título: |
Computational investigations in eukaryotes genome de novo assembly using short reads. |
|
Ano de publicação: |
2011 |
|
Fonte/Imprenta: |
In: INTERNATIONAL CONFERENCE OF THE BRAZILIAN ASSOCIATION FOR BIOINFORMATICS AND COMPUTATIONAL BIOLOGY, 7.; INTERNATIONAL CONFERENCE OF THE IBEROAMERICAN SOCIETY FOR BIOINFORMATICS, 3., 2011, Florianópolis. Proceedings... Florianópolis: Associação Brasileira de Bioinformática e Biologia Computacional, 2011. |
|
Páginas: |
Não paginado. |
|
Idioma: |
Inglês |
|
Notas: |
X-MEETING 2011. |
|
Conteúdo: |
Recently news technologies in molecular biology enormously improved the sequencing data production, making it possible to generate billions of short reads totalizing gibabases of data per experiment. Prices for sequencing are decreasing rapidly and experiments that were impossible in the past because of costs are now being executed. Computational methodologies that were successfully used to solve the genome assembler problem with data obtained by the shotgun strategy, are now inefficient. Efforts are under way to develop new programs. At this moment, a stabilized condition for producing quality assembles is to use paired-end reads to virtually increase the length of reads, but there is a lot of controversy in other points. The works described in literature basically use two strategies: one is based in a high coverage[1] and the other is based in an incremental assembly, using the made pairs with shorter inserts first[2]. Independently of the strategy used the computational resources demanded are actually very high. Basically the present computational solution for the de novo genome assembly involves the generation of a graph of some kind [3], and one because those graphs use as node whole reads or k-mers, and considering that the amount of reads is very expressive; it is possible to infer that the memory resource of the computational system will be very important. Works in literature corroborate this idea showing that multiprocessors computational systems with at least 512 Gb of principal memory were used in de novo projects of eukaryotes [1,2,3]. As an example and benchmark source it is possible use the Panda project, which was executed by a research group consortium at China and generated de novo genome of the giant Panda (Ailuropoda melanoleura) . The project initially produced 231 Gb of raw data, which was reduced to 176 Gb after removing low-quality and duplicated reads. In the de novo assembly process just 134 Gb were used. Those bases were distributed in approximately 3 billions short reads. After the assembly, 200604 contigs were generated and 5701 multicontig scaffolds were obtained using 124336 contigs. The N50 was respectively . 36728 bp and 1.22 Mb for contigs and scaffolds. The present work investigated the computational demands of de novo assembly of eukaryotes genomes, reproducing the results of the Panda project. The strategy used was incremental as implemented in the SOAPdenovo software, which basically divides the assembly process in four steps: pre-graph to construction of kmer-graph; contig to eliminate errors and output contigs, map to map reads in the contigs and scaff to scaffold contigs. It used a NUMA (non-uniform memory access) computational system with 8 six-core processors with hyperthread tecnology and 512 Gb of RAM (random access memory), and the consumption of resources as memory and processor time were pointed for every steps in the process. The incremental strategy to solve the problem seems practical and can produce effective results. At this moment a work is in progress which is investigating a new methodology to group the short reads together using the entropy concept. It is possible that assemblies with better quality will be generated, because this methodology initially uses more informative reads. References [1] Gnerre et. al.; High-quality draft assemblies of mammalian genomes from massively parallel sequence data, Proceedings of the National Academy of Sciences USA, v. 108, n. 4, p. 1513-1518, 2010 [2] Li et. al.; The sequence and de novo assembly of the giant panda genome, Nature, v. 463, p. 311-317, 2010 [3] Schatz et. al.; Assembly of large genomes using second-generation sequencing, Genome Research, v. 20, p. 1165-1173, 2010 MenosRecently news technologies in molecular biology enormously improved the sequencing data production, making it possible to generate billions of short reads totalizing gibabases of data per experiment. Prices for sequencing are decreasing rapidly and experiments that were impossible in the past because of costs are now being executed. Computational methodologies that were successfully used to solve the genome assembler problem with data obtained by the shotgun strategy, are now inefficient. Efforts are under way to develop new programs. At this moment, a stabilized condition for producing quality assembles is to use paired-end reads to virtually increase the length of reads, but there is a lot of controversy in other points. The works described in literature basically use two strategies: one is based in a high coverage[1] and the other is based in an incremental assembly, using the made pairs with shorter inserts first[2]. Independently of the strategy used the computational resources demanded are actually very high. Basically the present computational solution for the de novo genome assembly involves the generation of a graph of some kind [3], and one because those graphs use as node whole reads or k-mers, and considering that the amount of reads is very expressive; it is possible to infer that the memory resource of the computational system will be very important. Works in literature corroborate this idea showing that multiprocessors computational systems with at least 512 G... Mostrar Tudo |
|
Palavras-Chave: |
Bioinformática; Genomas de eucariotos. |
|
Thesagro: |
Biologia Molecular; Genoma. |
|
Thesaurus NAL: |
Bioinformatics; Eukaryotic cells; Genome; Molecular biology. |
|
Categoria do assunto: |
-- |
|
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/49471/1/eukariotes.pdf
|
|
Marc: |
LEADER 04672nam a2200229 a 4500
001 1908741
005 2020-01-24
008 2011 bl uuuu u00u1 u #d
100 1 $aCINTRA, L. C.
245 $aComputational investigations in eukaryotes genome de novo assembly using short reads.$h[electronic resource]
260 $aIn: INTERNATIONAL CONFERENCE OF THE BRAZILIAN ASSOCIATION FOR BIOINFORMATICS AND COMPUTATIONAL BIOLOGY, 7.; INTERNATIONAL CONFERENCE OF THE IBEROAMERICAN SOCIETY FOR BIOINFORMATICS, 3., 2011, Florianópolis. Proceedings... Florianópolis: Associação Brasileira de Bioinformática e Biologia Computacional$c2011
300 $aNão paginado.
500 $aX-MEETING 2011.
520 $aRecently news technologies in molecular biology enormously improved the sequencing data production, making it possible to generate billions of short reads totalizing gibabases of data per experiment. Prices for sequencing are decreasing rapidly and experiments that were impossible in the past because of costs are now being executed. Computational methodologies that were successfully used to solve the genome assembler problem with data obtained by the shotgun strategy, are now inefficient. Efforts are under way to develop new programs. At this moment, a stabilized condition for producing quality assembles is to use paired-end reads to virtually increase the length of reads, but there is a lot of controversy in other points. The works described in literature basically use two strategies: one is based in a high coverage[1] and the other is based in an incremental assembly, using the made pairs with shorter inserts first[2]. Independently of the strategy used the computational resources demanded are actually very high. Basically the present computational solution for the de novo genome assembly involves the generation of a graph of some kind [3], and one because those graphs use as node whole reads or k-mers, and considering that the amount of reads is very expressive; it is possible to infer that the memory resource of the computational system will be very important. Works in literature corroborate this idea showing that multiprocessors computational systems with at least 512 Gb of principal memory were used in de novo projects of eukaryotes [1,2,3]. As an example and benchmark source it is possible use the Panda project, which was executed by a research group consortium at China and generated de novo genome of the giant Panda (Ailuropoda melanoleura) . The project initially produced 231 Gb of raw data, which was reduced to 176 Gb after removing low-quality and duplicated reads. In the de novo assembly process just 134 Gb were used. Those bases were distributed in approximately 3 billions short reads. After the assembly, 200604 contigs were generated and 5701 multicontig scaffolds were obtained using 124336 contigs. The N50 was respectively . 36728 bp and 1.22 Mb for contigs and scaffolds. The present work investigated the computational demands of de novo assembly of eukaryotes genomes, reproducing the results of the Panda project. The strategy used was incremental as implemented in the SOAPdenovo software, which basically divides the assembly process in four steps: pre-graph to construction of kmer-graph; contig to eliminate errors and output contigs, map to map reads in the contigs and scaff to scaffold contigs. It used a NUMA (non-uniform memory access) computational system with 8 six-core processors with hyperthread tecnology and 512 Gb of RAM (random access memory), and the consumption of resources as memory and processor time were pointed for every steps in the process. The incremental strategy to solve the problem seems practical and can produce effective results. At this moment a work is in progress which is investigating a new methodology to group the short reads together using the entropy concept. It is possible that assemblies with better quality will be generated, because this methodology initially uses more informative reads. References [1] Gnerre et. al.; High-quality draft assemblies of mammalian genomes from massively parallel sequence data, Proceedings of the National Academy of Sciences USA, v. 108, n. 4, p. 1513-1518, 2010 [2] Li et. al.; The sequence and de novo assembly of the giant panda genome, Nature, v. 463, p. 311-317, 2010 [3] Schatz et. al.; Assembly of large genomes using second-generation sequencing, Genome Research, v. 20, p. 1165-1173, 2010
650 $aBioinformatics
650 $aEukaryotic cells
650 $aGenome
650 $aMolecular biology
650 $aBiologia Molecular
650 $aGenoma
653 $aBioinformática
653 $aGenomas de eucariotos
Download
Esconder MarcMostrar Marc Completo |
|
Registro original: |
Embrapa Agricultura Digital (CNPTIA) |
|
|
Biblioteca |
ID |
Origem |
Tipo/Formato |
Classificação |
Cutter |
Registro |
Volume |
Status |
Fechar
|
| Nenhum registro encontrado para a expressão de busca informada. |
|
|
