Beyond differential expression: the quest for causal mutations and effector molecules

<p>Abstract</p> <p>High throughput gene expression technologies are a popular choice for researchers seeking molecular or systems-level explanations of biological phenomena. Nevertheless, there has been a groundswell of opinion that these approaches have not lived up to the hype be...

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Main Authors: Hudson Nicholas J, Dalrymple Brian P, Reverter Antonio
Format: Article
Language:English
Published: BMC 2012-07-01
Series:BMC Genomics
Subjects:
Online Access:http://www.biomedcentral.com/1471-2164/13/356
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spelling doaj-0b2c4037b6544d17b1ef1bea65206c132020-11-25T01:39:17ZengBMCBMC Genomics1471-21642012-07-0113135610.1186/1471-2164-13-356Beyond differential expression: the quest for causal mutations and effector moleculesHudson Nicholas JDalrymple Brian PReverter Antonio<p>Abstract</p> <p>High throughput gene expression technologies are a popular choice for researchers seeking molecular or systems-level explanations of biological phenomena. Nevertheless, there has been a groundswell of opinion that these approaches have not lived up to the hype because the interpretation of the data has lagged behind its generation. In our view a major problem has been an over-reliance on isolated lists of differentially expressed (DE) genes which – by simply comparing genes to themselves – have the pitfall of taking molecular information out of context. Numerous scientists have emphasised the need for better context. This can be achieved through holistic measurements of differential connectivity in addition to, or in replacement, of DE. However, many scientists continue to use isolated lists of DE genes as the major source of input data for common readily available analytical tools. Focussing this opinion article on our own research in skeletal muscle, we outline our resolutions to these problems – particularly a universally powerful way of quantifying differential connectivity. With a well designed experiment, it is now possible to use gene expression to identify causal mutations and the other major effector molecules with whom they cooperate, irrespective of whether they themselves are DE. We explain why, for various reasons, no other currently available experimental techniques or quantitative analyses are capable of reaching these conclusions.</p> http://www.biomedcentral.com/1471-2164/13/356Differential connectivityDifferential networkingGene expressionCausal mutation algorithm
collection DOAJ
language English
format Article
sources DOAJ
author Hudson Nicholas J
Dalrymple Brian P
Reverter Antonio
spellingShingle Hudson Nicholas J
Dalrymple Brian P
Reverter Antonio
Beyond differential expression: the quest for causal mutations and effector molecules
BMC Genomics
Differential connectivity
Differential networking
Gene expression
Causal mutation algorithm
author_facet Hudson Nicholas J
Dalrymple Brian P
Reverter Antonio
author_sort Hudson Nicholas J
title Beyond differential expression: the quest for causal mutations and effector molecules
title_short Beyond differential expression: the quest for causal mutations and effector molecules
title_full Beyond differential expression: the quest for causal mutations and effector molecules
title_fullStr Beyond differential expression: the quest for causal mutations and effector molecules
title_full_unstemmed Beyond differential expression: the quest for causal mutations and effector molecules
title_sort beyond differential expression: the quest for causal mutations and effector molecules
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2012-07-01
description <p>Abstract</p> <p>High throughput gene expression technologies are a popular choice for researchers seeking molecular or systems-level explanations of biological phenomena. Nevertheless, there has been a groundswell of opinion that these approaches have not lived up to the hype because the interpretation of the data has lagged behind its generation. In our view a major problem has been an over-reliance on isolated lists of differentially expressed (DE) genes which – by simply comparing genes to themselves – have the pitfall of taking molecular information out of context. Numerous scientists have emphasised the need for better context. This can be achieved through holistic measurements of differential connectivity in addition to, or in replacement, of DE. However, many scientists continue to use isolated lists of DE genes as the major source of input data for common readily available analytical tools. Focussing this opinion article on our own research in skeletal muscle, we outline our resolutions to these problems – particularly a universally powerful way of quantifying differential connectivity. With a well designed experiment, it is now possible to use gene expression to identify causal mutations and the other major effector molecules with whom they cooperate, irrespective of whether they themselves are DE. We explain why, for various reasons, no other currently available experimental techniques or quantitative analyses are capable of reaching these conclusions.</p>
topic Differential connectivity
Differential networking
Gene expression
Causal mutation algorithm
url http://www.biomedcentral.com/1471-2164/13/356
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