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'PACLIMS': A component LIM system for high-throughput functional genomic analysis

BACKGROUND: Recent advances in sequencing techniques leading to cost reduction have resulted in the generation of a growing number of sequenced eukaryotic genomes. Computational tools greatly assist in defining open reading frames and assigning tentative annotations. However, gene functions cannot b...

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Autores principales: Donofrio, Nicole, Rajagopalon, Ravi, Brown, Douglas, Diener, Stephen, Windham, Donald, Nolin, Shelly, Floyd, Anna, Mitchell, Thomas, Galadima, Natalia, Tucker, Sara, Orbach, Marc J, Patel, Gayatri, Farman, Mark, Pampanwar, Vishal, Soderlund, Cari, Lee, Yong-Hwan, Dean, Ralph A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1090558/
https://www.ncbi.nlm.nih.gov/pubmed/15826298
http://dx.doi.org/10.1186/1471-2105-6-94
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author Donofrio, Nicole
Rajagopalon, Ravi
Brown, Douglas
Diener, Stephen
Windham, Donald
Nolin, Shelly
Floyd, Anna
Mitchell, Thomas
Galadima, Natalia
Tucker, Sara
Orbach, Marc J
Patel, Gayatri
Farman, Mark
Pampanwar, Vishal
Soderlund, Cari
Lee, Yong-Hwan
Dean, Ralph A
author_facet Donofrio, Nicole
Rajagopalon, Ravi
Brown, Douglas
Diener, Stephen
Windham, Donald
Nolin, Shelly
Floyd, Anna
Mitchell, Thomas
Galadima, Natalia
Tucker, Sara
Orbach, Marc J
Patel, Gayatri
Farman, Mark
Pampanwar, Vishal
Soderlund, Cari
Lee, Yong-Hwan
Dean, Ralph A
author_sort Donofrio, Nicole
collection PubMed
description BACKGROUND: Recent advances in sequencing techniques leading to cost reduction have resulted in the generation of a growing number of sequenced eukaryotic genomes. Computational tools greatly assist in defining open reading frames and assigning tentative annotations. However, gene functions cannot be asserted without biological support through, among other things, mutational analysis. In taking a genome-wide approach to functionally annotate an entire organism, in this application the ~11,000 predicted genes in the rice blast fungus (Magnaporthe grisea), an effective platform for tracking and storing both the biological materials created and the data produced across several participating institutions was required. RESULTS: The platform designed, named PACLIMS, was built to support our high throughput pipeline for generating 50,000 random insertion mutants of Magnaporthe grisea. To be a useful tool for materials and data tracking and storage, PACLIMS was designed to be simple to use, modifiable to accommodate refinement of research protocols, and cost-efficient. Data entry into PACLIMS was simplified through the use of barcodes and scanners, thus reducing the potential human error, time constraints, and labor. This platform was designed in concert with our experimental protocol so that it leads the researchers through each step of the process from mutant generation through phenotypic assays, thus ensuring that every mutant produced is handled in an identical manner and all necessary data is captured. CONCLUSION: Many sequenced eukaryotes have reached the point where computational analyses are no longer sufficient and require biological support for their predicted genes. Consequently, there is an increasing need for platforms that support high throughput genome-wide mutational analyses. While PACLIMS was designed specifically for this project, the source and ideas present in its implementation can be used as a model for other high throughput mutational endeavors.
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spelling pubmed-10905582005-05-07 'PACLIMS': A component LIM system for high-throughput functional genomic analysis Donofrio, Nicole Rajagopalon, Ravi Brown, Douglas Diener, Stephen Windham, Donald Nolin, Shelly Floyd, Anna Mitchell, Thomas Galadima, Natalia Tucker, Sara Orbach, Marc J Patel, Gayatri Farman, Mark Pampanwar, Vishal Soderlund, Cari Lee, Yong-Hwan Dean, Ralph A BMC Bioinformatics Software BACKGROUND: Recent advances in sequencing techniques leading to cost reduction have resulted in the generation of a growing number of sequenced eukaryotic genomes. Computational tools greatly assist in defining open reading frames and assigning tentative annotations. However, gene functions cannot be asserted without biological support through, among other things, mutational analysis. In taking a genome-wide approach to functionally annotate an entire organism, in this application the ~11,000 predicted genes in the rice blast fungus (Magnaporthe grisea), an effective platform for tracking and storing both the biological materials created and the data produced across several participating institutions was required. RESULTS: The platform designed, named PACLIMS, was built to support our high throughput pipeline for generating 50,000 random insertion mutants of Magnaporthe grisea. To be a useful tool for materials and data tracking and storage, PACLIMS was designed to be simple to use, modifiable to accommodate refinement of research protocols, and cost-efficient. Data entry into PACLIMS was simplified through the use of barcodes and scanners, thus reducing the potential human error, time constraints, and labor. This platform was designed in concert with our experimental protocol so that it leads the researchers through each step of the process from mutant generation through phenotypic assays, thus ensuring that every mutant produced is handled in an identical manner and all necessary data is captured. CONCLUSION: Many sequenced eukaryotes have reached the point where computational analyses are no longer sufficient and require biological support for their predicted genes. Consequently, there is an increasing need for platforms that support high throughput genome-wide mutational analyses. While PACLIMS was designed specifically for this project, the source and ideas present in its implementation can be used as a model for other high throughput mutational endeavors. BioMed Central 2005-04-12 /pmc/articles/PMC1090558/ /pubmed/15826298 http://dx.doi.org/10.1186/1471-2105-6-94 Text en Copyright © 2005 Donofrio et al; licensee BioMed Central Ltd.
spellingShingle Software
Donofrio, Nicole
Rajagopalon, Ravi
Brown, Douglas
Diener, Stephen
Windham, Donald
Nolin, Shelly
Floyd, Anna
Mitchell, Thomas
Galadima, Natalia
Tucker, Sara
Orbach, Marc J
Patel, Gayatri
Farman, Mark
Pampanwar, Vishal
Soderlund, Cari
Lee, Yong-Hwan
Dean, Ralph A
'PACLIMS': A component LIM system for high-throughput functional genomic analysis
title 'PACLIMS': A component LIM system for high-throughput functional genomic analysis
title_full 'PACLIMS': A component LIM system for high-throughput functional genomic analysis
title_fullStr 'PACLIMS': A component LIM system for high-throughput functional genomic analysis
title_full_unstemmed 'PACLIMS': A component LIM system for high-throughput functional genomic analysis
title_short 'PACLIMS': A component LIM system for high-throughput functional genomic analysis
title_sort 'paclims': a component lim system for high-throughput functional genomic analysis
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1090558/
https://www.ncbi.nlm.nih.gov/pubmed/15826298
http://dx.doi.org/10.1186/1471-2105-6-94
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