Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects

The recent genome initiatives of the neglected parasites Trypanosoma vivax and Trypanosoma congolense, and the vector tsetse are promising with regards to the data available in public databases. While these genome initiatives and the potential for developing new drugs and vaccines are admirable, it...

Descripción completa

Detalles Bibliográficos
Autores principales: Davila, A.M.R., Majiwa, Phelix A.O., Grisard, E.C., Aksoy, S., Hide, W.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Elsevier 2004
Materias:
Acceso en línea:https://hdl.handle.net/10568/29684
_version_ 1855538798166802432
author Davila, A.M.R.
Majiwa, Phelix A.O.
Grisard, E.C.
Aksoy, S.
Hide, W.
author_browse Aksoy, S.
Davila, A.M.R.
Grisard, E.C.
Hide, W.
Majiwa, Phelix A.O.
author_facet Davila, A.M.R.
Majiwa, Phelix A.O.
Grisard, E.C.
Aksoy, S.
Hide, W.
author_sort Davila, A.M.R.
collection Repository of Agricultural Research Outputs (CGSpace)
description The recent genome initiatives of the neglected parasites Trypanosoma vivax and Trypanosoma congolense, and the vector tsetse are promising with regards to the data available in public databases. While these genome initiatives and the potential for developing new drugs and vaccines are admirable, it is notable that scientists from developing and endemic countries have had very little participation in the process of developing genome resources that are important in their fight against disease. The capacity exists within disease-endemic countries (DECs) to contribute to annotation and development of the analyses of the parasite and vector genomes. It is stated that both bioinformatics and research are becoming more necessary and essential in DECs. Therefore, there is an urgent need to undertake bioinformatics capacity-building in developing countries for several reasons, such as: (i) costs for bioinformatics research are lower; (ii) annotations would be performed in close collaboration with the sequencing centers in developed countries; (iii) the biology of the organism (pathogens and pests) is evident in DECs; hence, relevant genes can be evaluated as soon as they are identified, thus speeding up the evaluation and validation phase of candidate genes; (iv) validation of reagents or biotechnological products can often be performed in DECs on definitive host(s) affected by the pathogen, without undue restrictions inherent in conducting such validations where the disease is not endemic (e.g. developed countries); (v) a sense of joint ownership can be developed over the information derived from the sequence; and (vi) re-annotation is usually necessary and can be also be performed in developing countries. Additional justification includes the need to develop capacity to address local problems locally. The process of annotation, not just access to raw sequence reads from a website, requires the development of skills that can be subsequently applied with high impact in the local environment.
format Journal Article
id CGSpace29684
institution CGIAR Consortium
language Inglés
publishDate 2004
publishDateRange 2004
publishDateSort 2004
publisher Elsevier
publisherStr Elsevier
record_format dspace
spelling CGSpace296842024-03-06T10:16:43Z Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects Davila, A.M.R. Majiwa, Phelix A.O. Grisard, E.C. Aksoy, S. Hide, W. glossina trypanosoma congolense trypanosoma vivax genomes nucleotide sequence research projects The recent genome initiatives of the neglected parasites Trypanosoma vivax and Trypanosoma congolense, and the vector tsetse are promising with regards to the data available in public databases. While these genome initiatives and the potential for developing new drugs and vaccines are admirable, it is notable that scientists from developing and endemic countries have had very little participation in the process of developing genome resources that are important in their fight against disease. The capacity exists within disease-endemic countries (DECs) to contribute to annotation and development of the analyses of the parasite and vector genomes. It is stated that both bioinformatics and research are becoming more necessary and essential in DECs. Therefore, there is an urgent need to undertake bioinformatics capacity-building in developing countries for several reasons, such as: (i) costs for bioinformatics research are lower; (ii) annotations would be performed in close collaboration with the sequencing centers in developed countries; (iii) the biology of the organism (pathogens and pests) is evident in DECs; hence, relevant genes can be evaluated as soon as they are identified, thus speeding up the evaluation and validation phase of candidate genes; (iv) validation of reagents or biotechnological products can often be performed in DECs on definitive host(s) affected by the pathogen, without undue restrictions inherent in conducting such validations where the disease is not endemic (e.g. developed countries); (v) a sense of joint ownership can be developed over the information derived from the sequence; and (vi) re-annotation is usually necessary and can be also be performed in developing countries. Additional justification includes the need to develop capacity to address local problems locally. The process of annotation, not just access to raw sequence reads from a website, requires the development of skills that can be subsequently applied with high impact in the local environment. 2004-07 2013-06-11T09:24:28Z 2013-06-11T09:24:28Z Journal Article https://hdl.handle.net/10568/29684 en Limited Access Elsevier Davila, A.M.R. 2004. Response to Hertz-Fowler and Berriman: Continuing tsetse and Trypanosoma genome sequencing projects. Trends in Parasitology;20(7): 309-310
spellingShingle glossina
trypanosoma congolense
trypanosoma vivax
genomes
nucleotide sequence
research projects
Davila, A.M.R.
Majiwa, Phelix A.O.
Grisard, E.C.
Aksoy, S.
Hide, W.
Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects
title Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects
title_full Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects
title_fullStr Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects
title_full_unstemmed Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects
title_short Response to Hertz-Fowler and Berriman: Continuing tsetse and trypanosoma genome sequencing projects
title_sort response to hertz fowler and berriman continuing tsetse and trypanosoma genome sequencing projects
topic glossina
trypanosoma congolense
trypanosoma vivax
genomes
nucleotide sequence
research projects
url https://hdl.handle.net/10568/29684
work_keys_str_mv AT davilaamr responsetohertzfowlerandberrimancontinuingtsetseandtrypanosomagenomesequencingprojects
AT majiwaphelixao responsetohertzfowlerandberrimancontinuingtsetseandtrypanosomagenomesequencingprojects
AT grisardec responsetohertzfowlerandberrimancontinuingtsetseandtrypanosomagenomesequencingprojects
AT aksoys responsetohertzfowlerandberrimancontinuingtsetseandtrypanosomagenomesequencingprojects
AT hidew responsetohertzfowlerandberrimancontinuingtsetseandtrypanosomagenomesequencingprojects