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Registro Completo |
Biblioteca(s): |
Embrapa Cerrados. |
Data corrente: |
11/02/1993 |
Data da última atualização: |
11/02/1993 |
Autoria: |
JABUONSKI, R. E.; TAKATSU, A.; REIFSCHNEIDER, F. J. B. |
Título: |
Avaliacao da patogenicidade de bacterias do genero Erwinia isoladas de batateira, tomateiro e de outras plantas hospedeiras. |
Ano de publicação: |
1986 |
Fonte/Imprenta: |
Fitopatologia Brasileira, v.11, n.3, p.587-597, 1986. |
Idioma: |
Português |
Palavras-Chave: |
Brasil; Brasilia; Distrito Federal; Lycopersicum esculentum. |
Thesagro: |
Bactéria; Batata; Cerrado; Doença; Patógeno; Solanum Tuberosum; Tomate. |
Thesaurus Nal: |
Erwinia. |
Categoria do assunto: |
-- |
Marc: |
LEADER 00780naa a2200277 a 4500 001 1547847 005 1993-02-11 008 1986 bl uuuu u00u1 u #d 100 1 $aJABUONSKI, R. E. 245 $aAvaliacao da patogenicidade de bacterias do genero Erwinia isoladas de batateira, tomateiro e de outras plantas hospedeiras. 260 $c1986 650 $aErwinia 650 $aBactéria 650 $aBatata 650 $aCerrado 650 $aDoença 650 $aPatógeno 650 $aSolanum Tuberosum 650 $aTomate 653 $aBrasil 653 $aBrasilia 653 $aDistrito Federal 653 $aLycopersicum esculentum 700 1 $aTAKATSU, A. 700 1 $aREIFSCHNEIDER, F. J. B. 773 $tFitopatologia Brasileira$gv.11, n.3, p.587-597, 1986.
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Embrapa Cerrados (CPAC) |
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Registro Completo
Biblioteca(s): |
Embrapa Agricultura Digital. |
Data corrente: |
21/11/2012 |
Data da última atualização: |
14/04/2020 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
PROTASIO, A. V.; TSAI, I. J.; BABBAGE, A.; NICHOL, S.; HUNT, M.; ASLETT, M. A.; SILVA, N. de; VELARDE, G. S.; ANDERSON, T. J. C.; CLARK, R. C.; DAVIDSON, C.; DILLON, G. P.; HOLROYD, N. E.; LOVERDE, P. T.; LLOYD, C.; MCQUILLAN, J.; OLIVEIRA, G.; OTTO, T. D.; PARKER-MANUEL, S. J.; QUAIL, M. A.; WILSON, R. A.; ZERLOTINI, A.; DUNNE, D. W.; BERRIMAN, M. |
Afiliação: |
ANNA V. PROTASIO, Wellcome Trust Sanger Institute; ISHENG J. TSAI, Wellcome Trust Sanger Institute; ANNE BABBAGE, Wellcome Trust Sanger Institute; SARAH NICHOL, Wellcome Trust Sanger Institute; MARTIN HUNT, Wellcome Trust Sanger Institute; MARTIN A. ASLETT, Wellcome Trust Sanger Institute; NISHADI DE SILVA, Wellcome Trust Sanger Institute; GILES S. VELARDE, Wellcome Trust Sanger Institute; TIM J. C. ANDERSON, Texas Biomedical Research Institute; RICHARD C. CLARK, Wellcome Trust Sanger Institute; CLAIRE DAVIDSON, Wellcome Trust Sanger Institute; GARY P. DILLON, Wellcome Trust Sanger Institute; NANCY E. HOLROYD, Wellcome Trust Sanger Institute; PHILIP T. LOVERDE, University of Texas Health Science Center; CHRISTINE LLOYD, Wellcome Trust Sanger Institute; JACQUELLINE MCQUILLAN, Wellcome Trust Sanger Institute; GUILHERME OLIVEIRA, Centro de Pesquisas René Rachou, Fundação Oswaldo Cruz; THOMAS D. OTTO, Wellcome Trust Sanger Institute; SOPHIA J. PARKER-MANUEL, University of York; MICHAEL A. QUAIL, Wellcome Trust Sanger Institute; R. ALAN WILSON, University of York; ADHEMAR ZERLOTINI NETO, CNPTIA; DAVID W. DUNNE, University of Cambridge; MATTHEW BERRIMAN, Wellcome Trust Sanger Institute. |
Título: |
A systematically improved high quality genome and transcriptome of the human blood fluke Schistosoma mansoni. |
Ano de publicação: |
2012 |
Fonte/Imprenta: |
PLOS Neglected Tropical Diseases, v. 6, n. 1, p. 1-13, Jan. 2012. |
DOI: |
10.1371/journal.pntd.0001455 |
Idioma: |
Inglês |
Conteúdo: |
Schistosomiasis is one of the most prevalent parasitic diseases, affecting millions of people in developing countries. Amongst the human-infective species, Schistosoma mansoni is also the most commonly used in the laboratory and here we present the systematic improvement of its draft genome. We used Sanger capillary and deep-coverage Illumina sequencing from clonal worms to upgrade the highly fragmented draft 380 Mb genome to one with only 885 scaffolds and more than 81% of the bases organised into chromosomes. We have also used transcriptome sequencing (RNA-seq) from four time points in the parasite?s life cycle to refine gene predictions and profile their expression. More than 45% of predicted genes have been extensively modified and the total number has been reduced from 11,807 to 10,852. Using the new version of the genome, we identified trans-splicing events occurring in at least 11% of genes and identified clear cases where it is used to resolve polycistronic transcripts. We have produced a high-resolution map of temporal changes in expression for 9,535 genes, covering an unprecedented dynamic range for this organism. All of these data have been consolidated into a searchable format within the GeneDB (www.genedb.org) and SchistoDB (www.schistodb.net) databases. With further transcriptional profiling and genome sequencing increasingly accessible, the upgraded genome will form a fundamental dataset to underpin further advances in schistosome research. |
Thesaurus NAL: |
Schistosoma. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/70531/1/journal.pntd.0001455.pdf
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Marc: |
LEADER 02660naa a2200421 a 4500 001 1940202 005 2020-04-14 008 2012 bl uuuu u00u1 u #d 024 7 $a10.1371/journal.pntd.0001455$2DOI 100 1 $aPROTASIO, A. V. 245 $aA systematically improved high quality genome and transcriptome of the human blood fluke Schistosoma mansoni.$h[electronic resource] 260 $c2012 520 $aSchistosomiasis is one of the most prevalent parasitic diseases, affecting millions of people in developing countries. Amongst the human-infective species, Schistosoma mansoni is also the most commonly used in the laboratory and here we present the systematic improvement of its draft genome. We used Sanger capillary and deep-coverage Illumina sequencing from clonal worms to upgrade the highly fragmented draft 380 Mb genome to one with only 885 scaffolds and more than 81% of the bases organised into chromosomes. We have also used transcriptome sequencing (RNA-seq) from four time points in the parasite?s life cycle to refine gene predictions and profile their expression. More than 45% of predicted genes have been extensively modified and the total number has been reduced from 11,807 to 10,852. Using the new version of the genome, we identified trans-splicing events occurring in at least 11% of genes and identified clear cases where it is used to resolve polycistronic transcripts. We have produced a high-resolution map of temporal changes in expression for 9,535 genes, covering an unprecedented dynamic range for this organism. All of these data have been consolidated into a searchable format within the GeneDB (www.genedb.org) and SchistoDB (www.schistodb.net) databases. With further transcriptional profiling and genome sequencing increasingly accessible, the upgraded genome will form a fundamental dataset to underpin further advances in schistosome research. 650 $aSchistosoma 700 1 $aTSAI, I. J. 700 1 $aBABBAGE, A. 700 1 $aNICHOL, S. 700 1 $aHUNT, M. 700 1 $aASLETT, M. A. 700 1 $aSILVA, N. de 700 1 $aVELARDE, G. S. 700 1 $aANDERSON, T. J. C. 700 1 $aCLARK, R. C. 700 1 $aDAVIDSON, C. 700 1 $aDILLON, G. P. 700 1 $aHOLROYD, N. E. 700 1 $aLOVERDE, P. T. 700 1 $aLLOYD, C. 700 1 $aMCQUILLAN, J. 700 1 $aOLIVEIRA, G. 700 1 $aOTTO, T. D. 700 1 $aPARKER-MANUEL, S. J. 700 1 $aQUAIL, M. A. 700 1 $aWILSON, R. A. 700 1 $aZERLOTINI, A. 700 1 $aDUNNE, D. W. 700 1 $aBERRIMAN, M. 773 $tPLOS Neglected Tropical Diseases$gv. 6, n. 1, p. 1-13, Jan. 2012.
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