A variance-stabilizing transformation for gene-expression microarray data
By Blythe Durbin, Johanna S. Hardin, Douglas M. Hawkins, David M. Rocke. Intelligent Systems in Molecular Biology, 2002
479 citations recorded by the source corpus.
Subfields: Artificial Intelligence, Molecular Biology, Statistics and Probability
View Paper: https://www.semanticscholar.org/paper/383fd5c8ae82d50861f33127e9c2a67cd9c9402a
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Artificial Intelligence
- Peng Qiu
- Wolfgang Huber
- Juan C. Caicedo
- M. Ravallion
- Shantanu Singh
- Anne E Carpenter
- Matthew E. Ritchie
- Simon M. Lin
In Molecular Biology
- Gordon K. Smyth
- Wolfgang Huber
- Matthew E. Ritchie
- Alicia Oshlack
- Simon M. Lin
- Juan C. Caicedo
- Anne E Carpenter
- Shantanu Singh
In Statistics and Probability
- Wolfgang Huber
- Alicia Oshlack
- Peng Qiu
- Juan C. Caicedo
- M. Ravallion
- Shantanu Singh
- Anne E Carpenter
- Simon M. Lin
Citations in the corpus
- GFOLD: a generalized fold change for ranking differentially expressed genes from RNA-seq data (2012, unknown): “In microarray analysis, a well-known variance stabilization method is fold change with offset (or start-log) (Durbin et al. , 2002; Ritchie et al. , 2007; Rocke and Durbin, 2003), which adds an offset before calculating fold changes.”
- Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis (2010, methodology): “A common way to check the homoscedasticity of the data is by visualizing the relations between mean and standard deviation [15,16].”
- Model-based variance-stabilizing transformation for Illumina microarray data (2008, methodology): “(6) have shown that the variance approaches infinity as the mean approaches zero when a log transformation is applied.”
- A Model-Based Background Adjustment for Oligonucleotide Expression Arrays (2004, unknown): “We base our approach on the model proposed by, for example, Durbin et al. (2002). Using replicate array data, Irizarry et al.”
- Data-analysis strategies for image-based cell profiling (2017, background): “Redundant features can diminish the signals of other more complementary features that are underrepresented, thus confounding downstream analysis.”
- A concave log-like transformation allowing non-positive values (2017, background): “4 Other log-like transformations have been proposed including the generalized log (Durbin et al., 2002), the log modulus (John and Draper, 1980), the log-linear hybrid (Rocke and Durbin, 2003) and the hyperlog (Bagwell, 2005).”
- A comparison of background correction methods for two-colour microarrays (2007, background): “ Durbin and Rocke (2004) have previously shown how an additive offset can behave as a simple but effective variance stabilizing transformation.”
- Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 (2014, unknown): “Alternative estimators can be found that are more stable than the standard calculation of fold change as the ratio of average observed values for each condition [53-55].”
- Three-parameter lognormal distribution ubiquitously found in cDNA microarray data and its application to parametric data treatment (2004, unknown): “In order to solve the intensity-dependence problem in determined ratios, Huber et al. and Durbin et al. [5, 6 ] produced a new scheme that recognizes the differences in mRNA levels, not in terms of ratios but in terms of the difference values in arsinh functions, which have stability in their statis”
- Stochastic Models Inspired by Hybridization Theory for Short Oligonucleotide Arrays (2004, unknown): “A slightly more complicated, additive background multiplicative measurement error (ABME) model has been proposed by, for example, Huber et al. (2002), Cui et al. (2003), and Durbin et al. (2002).”