Difference between revisions of "Literature Studies"

(Preprocessing high-throughput data)
(Imputation methods for missing values)
Line 67: Line 67:
  
 
=== Imputation methods for missing values ===
 
=== Imputation methods for missing values ===
 +
''' 1996 '''</br>
 +
* [[Partially parametric techniques for multiple imputation (Schenker)]]
 +
''' 1999 '''</br>
 +
* [[Imputing Missing Data for Gene Expression Arrays]]
 
''' 2001 '''</br>
 
''' 2001 '''</br>
* [[Missing value estimation methods for DNA microarrays]]
+
* [[Missing value estimation methods for DNA microarrays (Troyanskaya)]]
 
''' 2002 '''</br>
 
''' 2002 '''</br>
 
* [[Imputation of missing longitudinal data: a comparison of methods]]
 
* [[Imputation of missing longitudinal data: a comparison of methods]]
 +
''' 2003 ''</br>
 +
* [[A Bayesian missing value estimation method for gene expression profile data (Oba)]]
 +
''' 2005 ''</br>
 +
* [[Nonlinear PCA: a missing data approach (Scholz)]]
 +
''' 2007 '''</br>
 +
* [[pcaMethods—a bioconductor package providing PCA methods for incomplete data (Stacklies)]]
 +
* [[Sequential imputation for missing values (Verboven)]]
 
''' 2008 '''</br>
 
''' 2008 '''</br>
 
* [[Which missing value imputation method to use in expression profiles: a comparative study and two selection schemes]]
 
* [[Which missing value imputation method to use in expression profiles: a comparative study and two selection schemes]]
 
''' 2011 ''' </br>
 
''' 2011 ''' </br>
 +
* [[Iterative stepwise regression imputation using standard and robust methods (Templ)]]
 
* [[Missing values in mass spectrometry based metabolomics: an undervalued step in the data processing pipeline]]
 
* [[Missing values in mass spectrometry based metabolomics: an undervalued step in the data processing pipeline]]
 +
''' 2012 ''' </br>
 +
* [[MissForest—non-parametric missing value imputation for mixed-type data (Stekhoven)]]
 +
''' 2013 ''' </br>
 +
* [[Accounting for undetected compounds in statistical analyses of mass spectrometry ‘omic studies (Taylor)]]
 +
* [[Comparison of imputation methods for missing laboratory data in medicine (Waljee)]]
 
''' 2014 '''</br>
 
''' 2014 '''</br>
 +
* [[Comparison of Random Forest and Parametric Imputation Models for Imputing Missing Data Using MICE: A CALIBER Study (Shah)]]
 +
* [[Comparison of methods for imputing limited-range variables: a simulation study (Rodwell)]]
 +
* [[Tuning multiple imputation by predictive mean matching and local residual draws (Morris)]]
 
* [[Recursive partitioning for missing data imputation in the presence of interaction effects.]]
 
* [[Recursive partitioning for missing data imputation in the presence of interaction effects.]]
 
''' 2015 '''</br>
 
''' 2015 '''</br>
Line 83: Line 103:
 
* [[Multiple imputation and analysis for high-dimensional incomplete proteomics data]]
 
* [[Multiple imputation and analysis for high-dimensional incomplete proteomics data]]
 
''' 2018 '''</br>
 
''' 2018 '''</br>
* [[Missing Value Imputation Approach for Mass Spectrometry-based Metabolomics Data]]
+
* [[Missing Value Imputation Approach for Mass Spectrometry-based Metabolomics Data (Wei)]]
 +
* [[Gap-filling a spatially explicit plant trait database: comparing imputation methods and different levels of environmental information (Poyatos)]]
 +
* [[The effects of nonignorable missing data on label-free mass spectrometry proteomics experiments (O'Brien)]]
  
 
=== ODE-based Modelling ===
 
=== ODE-based Modelling ===

Revision as of 12:11, 25 February 2020

Page summary
Here outcomes of benchmarking studies from the literature are collected. The primary aim is a comprehensive overview about neutral benchmark studies, i.e. assessments which were performed independenty on publication of a new approach. Studies which are not neutral are put in brackets.

The focus is on computational methods for analyzing experimental data (instead of comparing experimental techniques or platforms).

Please extend this list by creating a new page and adding a link below.
Use the guidelines described here.

1 Results from Literature

1.1 Classification

2003

2005

2016

1.2 Selection of Differential Features and Regions

1.2.1 Identifying differential features

2006

2010

2017

2018

1.2.2 Identifying differential regions (e.g. DMRs)

2015

2016

2017

2018

1.2.3 Identifying sets of features (e.g. gene set analyses)

2009

2018

1.2.4 Dimension reduction

2008

2015

1.3 Imputation methods for missing values

1996

1999

2001

2002

' 2003

' 2005

2007

2008

2011

2012

2013

2014

2015

2016

2018

1.4 ODE-based Modelling

2001

2008

2011

2013

2017

2018

2019


2020

1.5 Omics Workflows

2015

2017

2019


1.6 Preprocessing high-throughput data

Year First Author Title
2003 A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
2005 Comparison of Affymetrix GeneChip Expression Measures
2005 Comparison of background correction and normalization procedures for high-density oligonucleotide microarrays
2006 Using RNA sample titrations to assess microarray platform performance and normalization techniques
2006 Wang P Normalization regarding non-random missing values in high-throughput mass spectrometry data
2007 Carvalho B Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data
2007 Cannataro M MS‐Analyzer: preprocessing and data mining services for proteomics applications on the Grid
2008 Comparison of preprocessing methods for the hgU133+2 chip from Affymetrix
2009 Comparison of Affymetrix data normalization methods using 6,926 experiments across five array generations
2010 Consistency of predictive signature genes and classifiers generated using different microarray platforms
2010 Detecting and correcting systematic variation in large-scale RNA sequencing data
2010 Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments
2010 Normalization of RNA-seq data using factor analysis of control genes or samples
2011 Affymetrix GeneChip microarray preprocessing for multivariate analyses
2012 A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysis
2014 Normalyzer: A Tool for Rapid Evaluation of Normalization Methods for Omics Data Sets
2014 Zhou X Prevention, diagnosis and treatment of high-throughput sequencing data pathologies
2015 Caraus I Detecting and overcoming systematic bias in high-throughput screening technologies: a comprehensive review of practical issues and methodological solutions
2015 Tam S Optimization of miRNA-seq data preprocessing
2016 Yi L Chemometric methods in data processing of mass spectrometry-based metabolomics: A review
2018 Mazoure B Identification and Correction of Additive and Multiplicative Spatial Biases in Experimental High-Throughput Screening