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                  <mods:namePart>Perkins, James Richard</mods:namePart>
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                  <mods:namePart>Dawes, John M</mods:namePart>
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                  <mods:namePart>McMahon, Steve B</mods:namePart>
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                  <mods:namePart>Bennett, David LH</mods:namePart>
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                  <mods:namePart>Orengo, Christine A.</mods:namePart>
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                  <mods:namePart>Kohl, Matthias</mods:namePart>
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               <mods:identifier type="citation">Perkins, J.R., Dawes, J.M., McMahon, S.B. et al. ReadqPCR and NormqPCR: R packages for the reading, quality checking and normalisation of RT-qPCR quantification cycle (Cq) data. BMC Genomics 13, 296 (2012). https://doi.org/10.1186/1471-2164-13-296</mods:identifier>
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               <mods:identifier type="doi">10.1186/1471-2164-13-296</mods:identifier>
               <mods:abstract>Background: Measuring gene transcription using real-time reverse transcription polymerase chain reaction (RT-qPCR) technology is a mainstay of molecular biology. Technologies now exist to measure the abundance of many transcripts in parallel. The selection of the optimal reference gene for the normalisation of this data is a recurring problem, and several algorithms have been developed in order to solve it. So far nothing in R exists to unite these methods, together with other functions to read in and normalise the data using the chosen reference gene(s).&#xd;
Results: We have developed two R/Bioconductor packages, ReadqPCR and NormqPCR, intended for a user with some experience with high-throughput data analysis using R, who wishes to use R to analyse RT-qPCR data. We illustrate their potential use in a workflow analysing a generic RT-qPCR experiment, and apply this to a real dataset. Packages are available from http://www.bioconductor.org/packages/release/bioc/html/ReadqPCR.htmland http://www.bioconductor.org/packages/release/bioc/html/NormqPCR.html&#xd;
Conclusions: These packages increase the repetoire of RT-qPCR analysis tools available to the R user and allow them to (amongst other things) read their data into R, hold it in an ExpressionSet compatible R object, choose appropriate reference genes, normalise the data and look for differential expression between samples.</mods:abstract>
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                  <mods:topic>Transcripción genética</mods:topic>
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                  <mods:topic>Genética molecular</mods:topic>
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                  <mods:title>ReadqPCR and NormqPCR: R packages for the reading, quality checking and normalisation of RT-qPCR quantification cycle (Cq) data</mods:title>
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