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1.
Mem. Inst. Oswaldo Cruz ; 92(6): 805-9, Nov.-Dec. 1997. ilus, tab
Artículo en Inglés | LILACS | ID: lil-197220

RESUMEN

Data analysis, presentation and distribution is of utmost importance to a genome project. A public domain software, AdDB, has been chosen as the common basis for parasite genome databases, and a first release of TcruziDB, the Trypanosoma cruzi genome database, is available by ftp from ftp://irisdbbm.fiocruz.br/pub/genomedb/TcruziDB as well as versions of the software for different operating systems (ftp://iris.dbbm.fiocruz.br/pub/unixsoft/). Morever, data originated from the project are available from the WWW server at http://www.dbbm.fiocruz.br. It contains biological and parasitological data on CL Brener, its karytype, all available T. cruzi sequences from Genbank, data on th EST-sequencing project and on available libraries, a T. cruzi codon table and a listing of activities and participating groups in the genome project, as well as meeting reports. T. cruzi discussion lists (tcruzi-l@iris.dbbm.fiocruz.br and tcgenics@iris.dbbm.fiocruz.br) being maintained for communication and to promote collaboration in the genome project.


Asunto(s)
Animales , Genoma de Protozoos , Sistemas de Información , Trypanosoma cruzi/genética , Redes de Comunicación de Computadores , Servicios de Información , Almacenamiento y Recuperación de la Información
2.
Mem. Inst. Oswaldo Cruz ; 92(6): 863-6, Nov.-Dec. 1997.
Artículo en Inglés | LILACS | ID: lil-197229

RESUMEN

Random single pass sequencing of cDNA fragments, also known as generation of Expressed Sequence Taggs (ESTs), has been highly successful in the study of the gene content of higher organisms, and forms an integral part of most genome projects, with the objective to identify new genes and targets for disease control and prevention and to generate mapping probes. In the Trypanosoma cruzi genome project, EST sequencing has also been a starting point, and here we report data on the first 797 sequences obtained, partly from a CL Brener epimastigote non-normalized library, partly on a normalized library. Only around 30 per cent of the sequences obtained showed similarity with Genbank and dbEST databases, half of which with sequences already reported for T. cruzi.


Asunto(s)
Animales , Biblioteca de Genes , Genoma de Protozoos , Trypanosoma cruzi/genética , Células Clonales
3.
Mem. Inst. Oswaldo Cruz ; 91(3): 279-284, May-Jun. 1996.
Artículo en Inglés | LILACS | ID: lil-319872

RESUMEN

Sequence analysis of Leishmania (Viannia) kDNA minicircles and analysis of multiple sequence alignments of the conserved region (minirepeats) of five distinct minicircles from L. (V.) braziliensis species with corresponding sequences derived from other dermotropic leishmanias indicated the presence of a sub-genus specific sequence. An oligonucleotide bearing this sequence was designed and used as a molecular probe, being able to recognize solely the sub-genus Viannia species in hybridization experiments. A dendrogram reflecting the homologies among the minirepeat sequences was constructed. Sequence clustering was obtained corresponding to the traditional classification based on similarity of biochemical, biological and parasitological characteristics of these Leishmania species, distinguishing the Old World dermotropic leishmanias, the New World dermotropic leishmanias of the sub-genus Leishmania and of the sub-genus Viannia.


Asunto(s)
Animales , ADN de Cinetoplasto , Leishmania , Oligonucleótidos , Secuencia de Bases , ADN de Cinetoplasto , Hibridación Genética , Leishmania , Leishmania braziliensis , Leishmania guyanensis , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , Análisis de Secuencia de ADN
4.
Mem. Inst. Oswaldo Cruz ; 88(2): 309-12, abr.-jun. 1993.
Artículo en Inglés | LILACS | ID: lil-119495

RESUMEN

The F508 mutation in the cystic fibrosis (CF) gene was studied in a population of 18 Brazilian CF patients and their 17 families by use of PCR and differential hybridization with oligonucleotides. In a total of 34 chromosomes considered, 12 (35%) carried the F508 deletion, a frequency much lower than that reported in most other populations. As a consequence, CF in Brazil would be predominantly caused by mutations different from the F508 deletion


Asunto(s)
Fibrosis Quística , Ingeniería Genética , Brasil
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