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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- A Bayesian missing value estimation method for gene expression profile data (1 link)
- A Systematic Evaluation of Single CellRNA-Seq Analysis Pipelines (1 link)
- A benchmarking of workflows for detecting differential splicing and differential expression at isoform level in human RNA-seq studies (1 link)
- A comparison of normalization methods for high density oligonucleotide array data based on variance and bias (1 link)
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the sequencing Quality control consortium (1 link)
- A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysis (1 link)
- A comprehensive evaluation of popular proteomics software workflows for label-free proteome quantification and imputation (1 link)
- A systematic evaluation of single-cell RNA-sequencing imputation methods (1 link)
- Accounting for undetected compounds in statistical analyses of mass spectrometry ‘omic studies (1 link)
- Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ* (1 link)
- Affymetrix GeneChip microarray preprocessing for multivariate analyses (1 link)
- Assessment of maximum likelihood PCA missing data imputation (1 link)
- Benchmarking scRNA-seq imputation tools with respect to network inference highlights deficits in performance at high levels of sparsity (1 link)
- Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays (1 link)
- Choice of library size normalization and statistical methods for differential gene expression analysis in balanced two-group comparisons for RNA-seq studies (1 link)
- Clustering of CyTOF Data (1 link)
- Comparative analysis of metagenomic classifiers for long-read sequencing datasets (1 link)
- Comparing Variant Call Files for Performance Benchmarkingof Next-Generation Sequencing Variant Calling Pipelines (1 link)
- Comparing feature selection methods for highdimensional imbalanced data: identifying rheumatoid arthritis cohorts from routine data (1 link)
- Comparison of Affymetrix GeneChip Expression Measures (1 link)