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Discovering collectively informative descriptors from high-throughput experiments

BACKGROUND: Improvements in high-throughput technology and its increasing use have led to the generation of many highly complex datasets that often address similar biological questions. Combining information from these studies can increase the reliability and generalizability of results and also yie...

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Autores principales: Jeffries, Clark D, Ward, William O, Perkins, Diana O, Wright, Fred A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813853/
https://www.ncbi.nlm.nih.gov/pubmed/20021653
http://dx.doi.org/10.1186/1471-2105-10-431
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author Jeffries, Clark D
Ward, William O
Perkins, Diana O
Wright, Fred A
author_facet Jeffries, Clark D
Ward, William O
Perkins, Diana O
Wright, Fred A
author_sort Jeffries, Clark D
collection PubMed
description BACKGROUND: Improvements in high-throughput technology and its increasing use have led to the generation of many highly complex datasets that often address similar biological questions. Combining information from these studies can increase the reliability and generalizability of results and also yield new insights that guide future research. RESULTS: This paper describes a novel algorithm called BLANKET for symmetric analysis of two experiments that assess informativeness of descriptors. The experiments are required to be related only in that their descriptor sets intersect substantially and their definitions of case and control are consistent. From resulting lists of n descriptors ranked by informativeness, BLANKET determines shortlists of descriptors from each experiment, generally of different lengths p and q. For any pair of shortlists, four numbers are evident: the number of descriptors appearing in both shortlists, in exactly one shortlist, or in neither shortlist. From the associated contingency table, BLANKET computes Right Fisher Exact Test (RFET) values used as scores over a plane of possible pairs of shortlist lengths [1,2]. BLANKET then chooses a pair or pairs with RFET score less than a threshold; the threshold depends upon n and shortlist length limits and represents a quality of intersection achieved by less than 5% of random lists. CONCLUSIONS: Researchers seek within a universe of descriptors some minimal subset that collectively and efficiently predicts experimental outcomes. Ideally, any smaller subset should be insufficient for reliable prediction and any larger subset should have little additional accuracy. As a method, BLANKET is easy to conceptualize and presents only moderate computational complexity. Many existing databases could be mined using BLANKET to suggest optimal sets of predictive descriptors.
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spelling pubmed-28138532010-01-30 Discovering collectively informative descriptors from high-throughput experiments Jeffries, Clark D Ward, William O Perkins, Diana O Wright, Fred A BMC Bioinformatics Methodology article BACKGROUND: Improvements in high-throughput technology and its increasing use have led to the generation of many highly complex datasets that often address similar biological questions. Combining information from these studies can increase the reliability and generalizability of results and also yield new insights that guide future research. RESULTS: This paper describes a novel algorithm called BLANKET for symmetric analysis of two experiments that assess informativeness of descriptors. The experiments are required to be related only in that their descriptor sets intersect substantially and their definitions of case and control are consistent. From resulting lists of n descriptors ranked by informativeness, BLANKET determines shortlists of descriptors from each experiment, generally of different lengths p and q. For any pair of shortlists, four numbers are evident: the number of descriptors appearing in both shortlists, in exactly one shortlist, or in neither shortlist. From the associated contingency table, BLANKET computes Right Fisher Exact Test (RFET) values used as scores over a plane of possible pairs of shortlist lengths [1,2]. BLANKET then chooses a pair or pairs with RFET score less than a threshold; the threshold depends upon n and shortlist length limits and represents a quality of intersection achieved by less than 5% of random lists. CONCLUSIONS: Researchers seek within a universe of descriptors some minimal subset that collectively and efficiently predicts experimental outcomes. Ideally, any smaller subset should be insufficient for reliable prediction and any larger subset should have little additional accuracy. As a method, BLANKET is easy to conceptualize and presents only moderate computational complexity. Many existing databases could be mined using BLANKET to suggest optimal sets of predictive descriptors. BioMed Central 2009-12-18 /pmc/articles/PMC2813853/ /pubmed/20021653 http://dx.doi.org/10.1186/1471-2105-10-431 Text en Copyright ©2009 Jeffries et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology article
Jeffries, Clark D
Ward, William O
Perkins, Diana O
Wright, Fred A
Discovering collectively informative descriptors from high-throughput experiments
title Discovering collectively informative descriptors from high-throughput experiments
title_full Discovering collectively informative descriptors from high-throughput experiments
title_fullStr Discovering collectively informative descriptors from high-throughput experiments
title_full_unstemmed Discovering collectively informative descriptors from high-throughput experiments
title_short Discovering collectively informative descriptors from high-throughput experiments
title_sort discovering collectively informative descriptors from high-throughput experiments
topic Methodology article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813853/
https://www.ncbi.nlm.nih.gov/pubmed/20021653
http://dx.doi.org/10.1186/1471-2105-10-431
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