Interesting times for microarray expression profiling.

Brief Funct Genomic Proteomic

Cancer Research UK Molecular Biology Core Facility, Paterson Institute for Cancer Research, University of Manchester, Withington, Manchester M20 4BX, UK.

Published: May 2009

AI Article Synopsis

  • Microarrays have evolved over the past decade from a limited technology used in a few research labs to a common method for expression profiling, now capable of assaying complete transcriptomes and single cells.
  • Advances in RNA labeling have made it possible to analyze samples even from formalin-fixed paraffin-embedded archival samples, making it a prime time for microarray core facilities.
  • However, the rise of Next Generation Sequencers, which can offer a more comprehensive view of cellular expression, poses a challenge to microarray dominance, though they are still not widely available enough to meet current demand.

Article Abstract

The last 10 years have seen microarrays go from being a nascent technology available only in a limited range of research facilities to becoming a ubiquitous approach to expression profiling. Developments in microarray technology have allowed the content of arrays to increase to the point that complete transcriptomes can be assayed on a single array, whilst developments in RNA labelling technology have reduced the amount of RNA needed down to the point where single cell profiling is technically possible. Recently it has also become possible to generate expression data from formalin-fixed paraffin-embedded archival samples. With the range of samples that can now be successfully profiled by microarray analysis this should be a good time to be running a microarray core facility. However, the arrival of Next Generation Sequencers means that for the first time there is an alternate platform that can potentially give a more complete picture of cellular expression than a microarray. Next Generation Sequencers are still in their infancy as a platform for expression profiling. Currently there are simply not enough Next Generation Sequencers in operation to meet the level of demand for expression profiling that microarray facilities service, but more systems are constantly becoming available. Looking ahead it seems certain that some proportion of expression profiling work will move from microarrays to Next Generation Sequencers, so now is a good time to consider some of the factors that might affect how significant that switch will be.

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Source
http://dx.doi.org/10.1093/bfgp/elp012DOI Listing

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