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Suggested Citation:"Glossary." National Research Council. 2006. Review of the Department of Energy's Genomics: GTL Program. Washington, DC: The National Academies Press. doi: 10.17226/11581.
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Glossary


Annotation1

Identification of the locations and coding regions of genes in a genome and determination of what they do.


Bioinformatics1

The study of genetic and other biological information using computer, mathematical, and statistical techniques.


Codon

A set of three adjoined nucleotides (triplet) that codes for an amino acid or a termination signal.


Functional genomics1

The study of genomes to determine the biological function of all the genes and their products.


Gene expression1

Conversion of the information encoded in a gene first to messenger RNA and then to a protein.

Genome1

The entire chromosomal genetic material of an organism.


Definitions taken from 1Science Vol. 291; 2NRC, 2003b; 3Handelsman, 2005b; 4NML, 2005; 5http://www.biochem.northwestern.edu/holmgren/Glossary/; 6http://www.medicine.net.com.

Suggested Citation:"Glossary." National Research Council. 2006. Review of the Department of Energy's Genomics: GTL Program. Washington, DC: The National Academies Press. doi: 10.17226/11581.
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Genomics1

The comprehensive study of whole sets of genes and their interactions rather than single genes or proteins.


High throughput2

Rapid (and simultaneous) processing of large sample sets.


Metabolomics2

The global analysis of metabolites and metabolic networks in cells, tissues, and organ systems.

Metagenomics3

The genomic analyses of assemblages of uncultured microorganisms.

Microarray2

A microscope slide or other solid support on which many distinct cDNAs or DNA oligonucleotides are patterned at high density in an addressable array. Microarrays are interrogated by hybridization to fluorescently labeled cDNAs or RNAs to detect the genes that are actively transcribed.


Open reading frame4

A reading frame in a sequence of nucleotides in DNA that contains no termination codons and so can potentially translate as a polypeptide chain.


PCR1

Polymerase chain reaction: a technique for amplifying a piece of DNA quickly and cheaply.

Proteomics1

The study of full set of proteins encoded by a genome.


Sequencing5

Determination of the order of nucleotides (base sequences) in a DNA or RNA molecule or the order of amino acids in a protein.

Shotgun assembly1

Breaking DNA into many small pieces, sequencing the pieces, and assembling the fragments.

Structural genomics1

The effort to determine the 3D structures of large numbers of proteins using both experimental techniques and computer simulation.


Upregulation6

An increase in the number of receptors on the surface of target cells, making the cells more sensitive to a hormone or another agent.

Suggested Citation:"Glossary." National Research Council. 2006. Review of the Department of Energy's Genomics: GTL Program. Washington, DC: The National Academies Press. doi: 10.17226/11581.
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Page 67
Suggested Citation:"Glossary." National Research Council. 2006. Review of the Department of Energy's Genomics: GTL Program. Washington, DC: The National Academies Press. doi: 10.17226/11581.
×
Page 68
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The U.S. Department of Energy (DOE) promotes scientific and technological innovation to advance the national, economic, and energy security of the United States. Recognizing the potential of microorganisms to offer new energy alternatives and remediate environmental contamination, DOE initiated the Genomes to Life program, now called Genomics: GTL, in 2000. The program aims to develop a predictive understanding of microbial systems that can be used to engineer systems for bioenergy production and environmental remediation, and to understand carbon cycling and sequestration. This report provides an evaluation of the program and its infrastructure plan. Overall, the report finds that GTL’s research has resulted in and promises to deliver many more scientific advancements that contribute to the achievement of DOE’s goals. However, the DOE’s current plan for building four independent facilities for protein production, molecular imaging, proteome analysis, and systems biology sequentially may not be the most cost-effective, efficient, and scientifically optimal way to provide this infrastructure. As an alternative, the report suggests constructing up to four institute-like facilities, each of which integrates the capabilities of all four of the originally planned facility types and focuses on one or two of DOE’s mission goals. The alternative infrastructure plan could have an especially high ratio of scientific benefit to cost because the need for technology will be directly tied to the biology goals of the program.

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