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 20 results in range #1 to #20.

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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)

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