Difference between revisions of "Literature Studies"
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=== Preprocessing high-throughput data=== | === Preprocessing high-throughput data=== | ||
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|- | |- | ||
| 2018 || Willforss J || [[NormalyzerDE: Online Tool for Improved Normalization of Omics Expression Data and High-Sensitivity Differential Expression Analysis]] | | 2018 || Willforss J || [[NormalyzerDE: Online Tool for Improved Normalization of Omics Expression Data and High-Sensitivity Differential Expression Analysis]] | ||
+ | |} | ||
+ | |||
+ | |||
+ | === Imputation methods for missing values === | ||
+ | |||
+ | {| class="wikitable sortable" | ||
+ | |- | ||
+ | ! Year || First Author || Title | ||
+ | |- | ||
+ | | 1996 || Schenker || [[Partially parametric techniques for multiple imputation]] | ||
+ | |- | ||
+ | | 1999 || Hastie T || [[Imputing Missing Data for Gene Expression Arrays]] | ||
+ | |- | ||
+ | | 2001 || Troyanskaya || [[Missing value estimation methods for DNA microarrays]] | ||
+ | |- | ||
+ | | 2002 || Engels J || [[Imputation of missing longitudinal data: a comparison of methods]] | ||
+ | |- | ||
+ | | 2003 || Oba || [[A Bayesian missing value estimation method for gene expression profile data]] | ||
+ | |- | ||
+ | | 2005 || Scholz || [[Nonlinear PCA: a missing data approach]] | ||
+ | |- | ||
+ | | 2007 || Stacklies || [[pcaMethods—a bioconductor package providing PCA methods for incomplete data]] | ||
+ | |- | ||
+ | | 2007 || Verboven || [[Sequential imputation for missing values]] | ||
+ | |- | ||
+ | | 2008 || Shaffer GN || [[Which missing value imputation method to use in expression profiles: a comparative study and two selection schemes]] | ||
+ | |- | ||
+ | | 2011 || Templ || [[Iterative stepwise regression imputation using standard and robust methods]] | ||
+ | |- | ||
+ | | 2012 || Hrydziuszko O || [[Missing values in mass spectrometry based metabolomics: an undervalued step in the data processing pipeline]] | ||
+ | |- | ||
+ | | 2012 || Stekhoven || [[MissForest—non-parametric missing value imputation for mixed-type data]] | ||
+ | |- | ||
+ | | 2013 || Taylor || [[Accounting for undetected compounds in statistical analyses of mass spectrometry ‘omic studies]] | ||
+ | |- | ||
+ | | 2013 || Waljee || [[Comparison of imputation methods for missing laboratory data in medicine]] | ||
+ | |- | ||
+ | | 2014 || Shah || [[Comparison of Random Forest and Parametric Imputation Models for Imputing Missing Data Using MICE: A CALIBER Study]] | ||
+ | |- | ||
+ | | 2014 || Rodwell || [[Comparison of methods for imputing limited-range variables: a simulation study]] | ||
+ | |- | ||
+ | | 2014 || Morris || [[Tuning multiple imputation by predictive mean matching and local residual draws]] | ||
+ | |- | ||
+ | | 2014 || Doove L || [[Recursive partitioning for missing data imputation in the presence of interaction effects]] | ||
+ | |- | ||
+ | | 2015 || Webb-Robertson BJM || [[Review, evaluation, and discussion of the challenges of missing value imputation for mass spectrometry-based label-free global proteomics]] | ||
+ | |- | ||
+ | | 2016 || Folch-Fortuny A || [[Assessment of maximum likelihood PCA missing data imputation]] | ||
+ | |- | ||
+ | | 2016 || Lazar C || [[Accounting for the Multiple Natures of Missing Values in Label-Free Quantitative Proteomics Data Sets to Compare Imputation Strategies]] | ||
+ | |- | ||
+ | | 2016 || Yin X || [[Multiple imputation and analysis for high-dimensional incomplete proteomics data]] | ||
+ | |- | ||
+ | | 2018 || Wei R || [[Missing Value Imputation Approach for Mass Spectrometry-based Metabolomics Data]] | ||
+ | |- | ||
+ | | 2018 || Poyatos R || [[Gap-filling a spatially explicit plant trait database: comparing imputation methods and different levels of environmental information]] | ||
+ | |- | ||
+ | | 2018 || O'Brien JJ || [[The effects of nonignorable missing data on label-free mass spectrometry proteomics experiments]] | ||
+ | |- | ||
+ | | 2021 || Jin L || [[A comparative study of evaluating missing value imputation methods in label-free proteomics]] | ||
+ | |} | ||
+ | |||
+ | === Omics Workflows === | ||
+ | {| class="wikitable sortable" | ||
+ | |- | ||
+ | ! Year || First Author || Title | ||
+ | |- | ||
+ | | 2008 || Neuweger H || [[MeltDB: a software platform for the analysis and integration of metabolomics experiment data]] | ||
+ | |- | ||
+ | | 2008 || Barla A || [[Machine learning methods for predictive proteomics]] | ||
+ | |- | ||
+ | | 2009 || Xia J || [[MetaboAnalyst: a web server for metabolomic data analysis and interpretation]] | ||
+ | |- | ||
+ | | 2013 || Weisser H || [[An Automated Pipeline for High-Throughput Label-Free Quantitative Proteomics]] | ||
+ | |- | ||
+ | | 2014 || Cox J || [[Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ* ]] | ||
+ | |- | ||
+ | | 2015 || Cleary || [[Comparing Variant Call Files for Performance Benchmarkingof Next-Generation Sequencing Variant Calling Pipelines]] | ||
+ | |- | ||
+ | | 2016 || Tyanova S || [[The MaxQuant computational platform for mass spectrometry–based shotgun proteomics]] | ||
+ | |- | ||
+ | | 2016 || Röst HL || [[OpenMS: a flexible open-source software platform for mass spectrometry data analysis]] | ||
+ | |- | ||
+ | | 2017 || Merino || [[A benchmarking of workflows for detecting differential splicing and differential expression at isoform level in human RNA-seq studies]] | ||
+ | |- | ||
+ | | 2018 || Välikangas T || [[A comprehensive evaluation of popular proteomics software workflows for label-free proteome quantification and imputation]] | ||
+ | |- | ||
+ | | 2019 || Vieth || [[A Systematic Evaluation of Single CellRNA-Seq Analysis Pipelines]] | ||
+ | |- | ||
+ | | 2019 || Krishnan || [[Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays]] | ||
+ | |- | ||
+ | | 2020 || Tang || [[Simultaneous Improvement in the Precision, Accuracy and Robustness of Label-free Proteome Quantification by Optimizing Data Manipulation Chains]] | ||
|} | |} | ||
Revision as of 14:38, 2 February 2021
Page summary |
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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 form the molecular biology field (instead of comparing experimental techniques or platforms). Please extend this list by creating a new page and adding a link below. |
Contents
1 Results from Literature
1.1 Classification
Year | First Author | Title |
---|---|---|
2003 | Wu | Comparison of statistical methods for classification of ovarian cancer using mass spectrometry data |
2005 | Bellaachia | Predicting Breast Cancer Survivability Using Data Mining Techniques |
1.2 Selection of Differential Features and Regions
1.2.1 Identifying differential features
1.2.2 Identifying differential regions (e.g. DMRs)
1.2.3 Identifying sets of features (e.g. gene set analyses)
Year | First Author | Title |
---|---|---|
2009 | Ackermann | A general modular framework for gene set enrichment analysis |
2009 | Tintle | Comparing gene set analysis methods on single-nucleotide polymorphism data from Genetic Analysis Workshop 16 |
2018 | Mathur | Gene set analysis methods: a systematic comparison |
2020 | Geistlinger | Toward a gold standard for benchmarking gene set enrichment analysis |
1.2.4 Dimension reduction
Year | First Author | Title |
---|---|---|
2008 | Janecek | On the Relationship Between Feature Selection and Classification Accuracy |
2015 | Fernández-Gutiérrez | Comparing feature selection methods for highdimensional imbalanced data: identifying rheumatoid arthritis cohorts from routine data |
1.3 Preprocessing high-throughput data
1.4 Imputation methods for missing values
1.5 Omics Workflows