The following pages link to BMC Bioinformatics (Q58840):
Displaying 50 items.
- GWAS on your notebook: fast semi-parallel linear and logistic regression for genome-wide association studies (Q58845) (← links)
- Block Forests: random forests for blocks of clinical and omics covariate data (Q59096) (← links)
- SQMtools: automated processing and visual analysis of ’omics data with R and anvi’o (Q64143) (← links)
- Genomic prediction using subsampling (Q66346) (← links)
- Bias in random forest variable importance measures: Illustrations, sources and a solution (Q69043) (← links)
- diceR: an R package for class discovery using an ensemble driven approach (Q70295) (← links)
- Single cell lineage reconstruction using distance-based algorithms and the R package, DCLEAR (Q75357) (← links)
- Simultaneous fitting of real-time PCR data with efficiency of amplification modeled as Gaussian function of target fluorescence (Q75819) (← links)
- chngpt: threshold regression model estimation and inference (Q78524) (← links)
- WGCNA: an R package for weighted correlation network analysis (Q80772) (← links)
- GENLIB: an R package for the analysis of genealogical data (Q80855) (← links)
- Bagging survival tree procedure for variable selection and prediction in the presence of nonsusceptible patients (Q81699) (← links)
- RNAstructure: software for RNA secondary structure prediction and analysis (Q81763) (← links)
- BPG: Seamless, automated and interactive visualization of scientific data (Q82714) (← links)
- tcR: an R package for T cell receptor repertoire advanced data analysis (Q85004) (← links)
- The curvHDR method for gating flow cytometry samples (Q88249) (← links)
- Extension of the bayesian alphabet for genomic selection (Q88580) (← links)
- A population-level statistic for assessing Mendelian behavior of genotyping-by-sequencing data from highly duplicated genomes (Q90617) (← links)
- QuickPed: an online tool for drawing pedigrees and analysing relatedness (Q96683) (← links)
- Computer-aided identification of polymorphism sets diagnostic for groups of bacterial and viral genetic variants (Q98634) (← links)
- PLEK: a tool for predicting long non-coding RNAs and messenger RNAs based on an improved k-mer scheme (Q98709) (← links)
- Feature selection for high-dimensional temporal data (Q98867) (← links)
- IntLIM: integration using linear models of metabolomics and gene expression data (Q99392) (← links)
- driveR: a novel method for prioritizing cancer driver genes using somatic genomics data (Q100202) (← links)
- A new multitest correction (SGoF) that increases its statistical power when increasing the number of tests (Q104264) (← links)
- A whitening approach to probabilistic canonical correlation analysis for omics data integration (Q106201) (← links)
- An integrated workflow for robust alignment and simplified quantitative analysis of NMR spectrometry data (Q107940) (← links)
- More powerful significant testing for time course gene expression data using functional principal component analysis approaches (Q110283) (← links)
- Significance testing in ridge regression for genetic data (Q111502) (← links)
- Random generalized linear model: a highly accurate and interpretable ensemble predictor (Q111528) (← links)
- Bayesian variable selection for high-dimensional data with an ordinal response: identifying genes associated with prognostic risk group in acute myeloid leukemia (Q111753) (← links)
- Analytical results on the Beauchemin model of lymphocyte migration (Q112719) (← links)
- BLAST+: architecture and applications (Q112884) (← links)
- Merged consensus clustering to assess and improve class discovery with microarray data (Q114321) (← links)
- Data-based RNA-seq simulations by binomial thinning (Q114599) (← links)
- Single sample scoring of molecular phenotypes (Q114721) (← links)
- Predicting RNA-binding sites of proteins using support vector machines and evolutionary information (Q117035) (← links)
- Conditional permutation importance revisited (Q121725) (← links)
- Statistical analysis of a Bayesian classifier based on the expression of miRNAs (Q125907) (← links)
- Integrating omics datasets with the OmicsPLS package (Q126049) (← links)
- Statistical integration of two omics datasets using GO2PLS (Q126052) (← links)
- GSVA: gene set variation analysis for microarray and RNA-Seq data (Q126221) (← links)
- Prediction of Human Phenotype Ontology terms by means of hierarchical ensemble methods (Q130237) (← links)
- flippant–An R package for the automated analysis of fluorescence-based scramblase assays (Q130477) (← links)
- Iterative pruning PCA improves resolution of highly structured populations (Q130976) (← links)
- simplePHENOTYPES: SIMulation of pleiotropic, linked and epistatic phenotypes (Q131158) (← links)
- NEAT: an efficient network enrichment analysis test (Q131769) (← links)
- Robust detection of periodic time series measured from biological systems (Q131909) (← links)
- Robust regression for periodicity detection in non-uniformly sampled time-course gene expression data (Q131912) (← links)
- PACVr: plastome assembly coverage visualization in R (Q132831) (← links)
