Wanted pages

List of non-existing pages with the most links to them, excluding pages which only have redirects linking to them. For a list of non-existent pages that have redirects linking to them, see the list of broken redirects.

Showing below up to 50 results in range #1 to #50.

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  1. A Bayesian missing value estimation method for gene expression profile data‏‎ (1 link)
  2. A Systematic Evaluation of Single CellRNA-Seq Analysis Pipelines‏‎ (1 link)
  3. A benchmarking of workflows for detecting differential splicing and differential expression at isoform level in human RNA-seq studies‏‎ (1 link)
  4. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias‏‎ (1 link)
  5. A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the sequencing Quality control consortium‏‎ (1 link)
  6. A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysis‏‎ (1 link)
  7. A comprehensive evaluation of popular proteomics software workflows for label-free proteome quantification and imputation‏‎ (1 link)
  8. A systematic evaluation of single-cell RNA-sequencing imputation methods‏‎ (1 link)
  9. Accounting for undetected compounds in statistical analyses of mass spectrometry ‘omic studies‏‎ (1 link)
  10. Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ*‏‎ (1 link)
  11. Affymetrix GeneChip microarray preprocessing for multivariate analyses‏‎ (1 link)
  12. Assessment of maximum likelihood PCA missing data imputation‏‎ (1 link)
  13. Benchmarking scRNA-seq imputation tools with respect to network inference highlights deficits in performance at high levels of sparsity‏‎ (1 link)
  14. Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays‏‎ (1 link)
  15. Choice of library size normalization and statistical methods for differential gene expression analysis in balanced two-group comparisons for RNA-seq studies‏‎ (1 link)
  16. Clustering of CyTOF Data‏‎ (1 link)
  17. Comparative analysis of metagenomic classifiers for long-read sequencing datasets‏‎ (1 link)
  18. Comparing Variant Call Files for Performance Benchmarkingof Next-Generation Sequencing Variant Calling Pipelines‏‎ (1 link)
  19. Comparing feature selection methods for highdimensional imbalanced data: identifying rheumatoid arthritis cohorts from routine data‏‎ (1 link)
  20. Comparison of Affymetrix GeneChip Expression Measures‏‎ (1 link)
  21. Comparison of Affymetrix data normalization methods using 6,926 experiments across five array generations‏‎ (1 link)
  22. Comparison of Computational Methods for Imputing Single-Cell RNA-Sequencing Data‏‎ (1 link)
  23. Comparison of Random Forest and Parametric Imputation Models for Imputing Missing Data Using MICE: A CALIBER Study‏‎ (1 link)
  24. Comparison of background correction and normalization procedures for high-density oligonucleotide microarrays‏‎ (1 link)
  25. Comparison of imputation methods for missing laboratory data in medicine‏‎ (1 link)
  26. Comparison of methods for imputing limited-range variables: a simulation study‏‎ (1 link)
  27. Comparison of preprocessing methods for the hgU133+2 chip from Affymetrix‏‎ (1 link)
  28. Consistency of predictive signature genes and classifiers generated using different microarray platforms‏‎ (1 link)
  29. De novo identification of differentially methylated regions in the human genome‏‎ (1 link)
  30. Detecting and correcting systematic variation in large-scale RNA sequencing data‏‎ (1 link)
  31. Evaluating the Performance of the Generalized Linear Model (glm) R Package Using Single-Cell RNA-Sequencing Data‏‎ (1 link)
  32. Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments‏‎ (1 link)
  33. Gap-filling a spatially explicit plant trait database: comparing imputation methods and different levels of environmental information‏‎ (1 link)
  34. Identification of Differentially Methylated Sites with Weak Methylation Effects‏‎ (1 link)
  35. Identification of differentially expressed peptides in high-throughput proteomics data‏‎ (1 link)
  36. Imputation of missing longitudinal data: a comparison of methods‏‎ (1 link)
  37. Imputing Missing Data for Gene Expression Arrays‏‎ (1 link)
  38. In-depth method assessments of differentially expressed protein detection for shotgun proteomics data with missing values‏‎ (1 link)
  39. Iterative stepwise regression imputation using standard and robust methods‏‎ (1 link)
  40. MethylAction: detecting differentially methylated regions that distinguish biological subtypes‏‎ (1 link)
  41. Metilene: Fast and sensitive calling of differentially methylated regions from bisulfite sequencing data‏‎ (1 link)
  42. MissForest—non-parametric missing value imputation for mixed-type data‏‎ (1 link)
  43. Missing Value Imputation Approach for Mass Spectrometry-based Metabolomics Data‏‎ (1 link)
  44. Multiple imputation and analysis for high-dimensional incomplete proteomics data‏‎ (1 link)
  45. Nonlinear PCA: a missing data approach‏‎ (1 link)
  46. Normalization of RNA-seq data using factor analysis of control genes or samples‏‎ (1 link)
  47. Normalyzer: A Tool for Rapid Evaluation of Normalization Methods for Omics Data Sets‏‎ (1 link)
  48. ODE parameter inference using adaptive gradient matching with Gaussian processes‏‎ (1 link)
  49. On the Relationship Between Feature Selection and Classification Accuracy‏‎ (1 link)
  50. Optimization of high dimensionsional ODEs‏‎ (1 link)

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