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Rscreenorm: normalization of CRISPR and siRNA screen data for more reproducible hit selection
by
Wolthuis, Rob M. F.
, Brakenhoff, Ruud H.
, van der Mijn, Johannes C.
, van Wieringen, Wessel N.
, van Beusechem, Victor W.
, Felley-Bosco, Emanuela
, Stoepker, Chantal
, de Menezes, Renée X.
, Verheul, Henk M. W.
, Bachas, Costa
, Hodzic, Jasmina
in
Algorithms
/ Analysis
/ Bioinformatics
/ Biomedical and Life Sciences
/ Biotechnology
/ Cancer
/ Cell lines
/ Comparative genomics
/ Computational Biology/Bioinformatics
/ Computer Appl. in Life Sciences
/ CRISPR
/ CRISPR-Cas systems
/ Data analysis
/ Data processing
/ Functional genomics
/ Genes
/ Genetic analysis
/ Genetic research
/ Genetic screening
/ Genomes
/ Genomics
/ Information management
/ Life Sciences
/ Methodology
/ Methodology Article
/ Methods
/ Microarrays
/ Normalization
/ Parameter estimation
/ Reproducibility
/ siRNA
/ Small interfering RNA
/ Statistical methods
/ Studies
2018
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Rscreenorm: normalization of CRISPR and siRNA screen data for more reproducible hit selection
by
Wolthuis, Rob M. F.
, Brakenhoff, Ruud H.
, van der Mijn, Johannes C.
, van Wieringen, Wessel N.
, van Beusechem, Victor W.
, Felley-Bosco, Emanuela
, Stoepker, Chantal
, de Menezes, Renée X.
, Verheul, Henk M. W.
, Bachas, Costa
, Hodzic, Jasmina
in
Algorithms
/ Analysis
/ Bioinformatics
/ Biomedical and Life Sciences
/ Biotechnology
/ Cancer
/ Cell lines
/ Comparative genomics
/ Computational Biology/Bioinformatics
/ Computer Appl. in Life Sciences
/ CRISPR
/ CRISPR-Cas systems
/ Data analysis
/ Data processing
/ Functional genomics
/ Genes
/ Genetic analysis
/ Genetic research
/ Genetic screening
/ Genomes
/ Genomics
/ Information management
/ Life Sciences
/ Methodology
/ Methodology Article
/ Methods
/ Microarrays
/ Normalization
/ Parameter estimation
/ Reproducibility
/ siRNA
/ Small interfering RNA
/ Statistical methods
/ Studies
2018
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Rscreenorm: normalization of CRISPR and siRNA screen data for more reproducible hit selection
by
Wolthuis, Rob M. F.
, Brakenhoff, Ruud H.
, van der Mijn, Johannes C.
, van Wieringen, Wessel N.
, van Beusechem, Victor W.
, Felley-Bosco, Emanuela
, Stoepker, Chantal
, de Menezes, Renée X.
, Verheul, Henk M. W.
, Bachas, Costa
, Hodzic, Jasmina
in
Algorithms
/ Analysis
/ Bioinformatics
/ Biomedical and Life Sciences
/ Biotechnology
/ Cancer
/ Cell lines
/ Comparative genomics
/ Computational Biology/Bioinformatics
/ Computer Appl. in Life Sciences
/ CRISPR
/ CRISPR-Cas systems
/ Data analysis
/ Data processing
/ Functional genomics
/ Genes
/ Genetic analysis
/ Genetic research
/ Genetic screening
/ Genomes
/ Genomics
/ Information management
/ Life Sciences
/ Methodology
/ Methodology Article
/ Methods
/ Microarrays
/ Normalization
/ Parameter estimation
/ Reproducibility
/ siRNA
/ Small interfering RNA
/ Statistical methods
/ Studies
2018
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Rscreenorm: normalization of CRISPR and siRNA screen data for more reproducible hit selection
Journal Article
Rscreenorm: normalization of CRISPR and siRNA screen data for more reproducible hit selection
2018
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Overview
Background
Reproducibility of hits from independent CRISPR or siRNA screens is poor. This is partly due to data normalization primarily addressing technical variability within independent screens, and not the technical differences between them.
Results
We present “rscreenorm”, a method that standardizes the functional data ranges between screens using assay controls, and subsequently performs a piecewise-linear normalization to make data distributions across all screens comparable. In simulation studies, rscreenorm reduces false positives. Using two multiple-cell lines siRNA screens, rscreenorm increased reproducibility between 27 and 62% for hits, and up to 5-fold for non-hits. Using publicly available CRISPR-Cas screen data, application of commonly used median centering yields merely 34% of overlapping hits, in contrast with rscreenorm yielding 84% of overlapping hits. Furthermore, rscreenorm yielded at most 8% discordant results, whilst median-centering yielded as much as 55%.
Conclusions
Rscreenorm yields more consistent results and keeps false positive rates under control, improving reproducibility of genetic screens data analysis from multiple cell lines.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
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