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  • Individual cells represent the basic unit in tissues and organisms and are in many aspects unique in their properties. The introduction of new and sensitive techniques to study single-cells opens up new avenues to understand fundamental biological processes. Well established statistical tools and recommendations exist for gene expression data based on traditional cell population measurements. However, these workflows are not suitable, and some steps are even inappropriate, to apply on single-cell data. Here, we present a simple and practical workflow for preprocessing of single-cell data generated by reverse transcription quantitative real-time PCR. The approach is demonstrated on a data set based on profiling of 41 genes in 303 single-cells. For some pre-processing steps we present options and also recommendations. In particular, we demonstrate and discuss different strategies for handling missing data and scaling data for downstream multivariate analysis. The aim of this workflow is provide guide to the rapidly growing community studying single-cells by means of reverse transcription quantitative real-time PCR profiling. (C) 2012 Elsevier Inc. All rights reserved.
  • Individual cells represent the basic unit in tissues and organisms and are in many aspects unique in their properties. The introduction of new and sensitive techniques to study single-cells opens up new avenues to understand fundamental biological processes. Well established statistical tools and recommendations exist for gene expression data based on traditional cell population measurements. However, these workflows are not suitable, and some steps are even inappropriate, to apply on single-cell data. Here, we present a simple and practical workflow for preprocessing of single-cell data generated by reverse transcription quantitative real-time PCR. The approach is demonstrated on a data set based on profiling of 41 genes in 303 single-cells. For some pre-processing steps we present options and also recommendations. In particular, we demonstrate and discuss different strategies for handling missing data and scaling data for downstream multivariate analysis. The aim of this workflow is provide guide to the rapidly growing community studying single-cells by means of reverse transcription quantitative real-time PCR profiling. (C) 2012 Elsevier Inc. All rights reserved. (en)
Title
  • RT-qPCR work-flow for single-cell data analysis
  • RT-qPCR work-flow for single-cell data analysis (en)
skos:prefLabel
  • RT-qPCR work-flow for single-cell data analysis
  • RT-qPCR work-flow for single-cell data analysis (en)
skos:notation
  • RIV/86652036:_____/13:00392069!RIV14-MSM-86652036
http://linked.open...avai/riv/aktivita
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  • I, P(GAP303/10/1338), P(ME10052), Z(AV0Z50520701)
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  • 1
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  • 103721
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  • RIV/86652036:_____/13:00392069
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  • RT-qPCR; Single-cell biology; Single-cell data analysis (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
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  • [B66C58B408CB]
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  • Methods
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  • 59
http://linked.open...iv/tvurceVysledku
  • Kubista, Mikael
  • Stahlberg, A.
  • Rusňáková, Vendula
  • Anděrová, Miroslava
  • Forootan, A.
http://linked.open...ain/vavai/riv/wos
  • 000314555700009
http://linked.open...n/vavai/riv/zamer
issn
  • 1046-2023
number of pages
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