The following pages link to Bioinformatics (Q58720):
Displaying 50 items.
- GWASinlps: non-local prior based iterative SNP selection tool for genome-wide association studies (Q87908) (← links)
- Edlib: a C/C ++ library for fast, exact sequence alignment using edit distance (Q88254) (← links)
- Pkgndep: a tool for analyzing dependency heaviness of R packages (Q89500) (← links)
- A latent unknown clustering integrating multi-omics data (LUCID) with phenotypic traits (Q90198) (← links)
- Network-based pathway enrichment analysis with incomplete network information (Q92134) (← links)
- Priors for Genotyping Polyploids (Q93200) (← links)
- Robust and sparse correlation matrix estimation for the analysis of high-dimensional genomics data (Q93489) (← links)
- SEMgraph: an R package for causal network inference of high-throughput data with structural equation models (Q93858) (← links)
- Robust rank aggregation for gene list integration and meta-analysis (Q94760) (← links)
- Multiple testing in genome-wide association studies via hidden Markov models (Q94930) (← links)
- Change-O: a toolkit for analyzing large-scale B cell immunoglobulin repertoire sequencing data (Q95128) (← links)
- A spectral clustering-based method for identifying clones from high-throughput B cell repertoire sequencing data (Q95974) (← links)
- Missing value estimation for DNA microarray gene expression data: local least squares imputation (Q96472) (← links)
- Learning sparse log-ratios for high-throughput sequencing data (Q98454) (← links)
- De novo construction of polyploid linkage maps using discrete graphical models (Q98897) (← links)
- ontologyX: a suite of R packages for working with ontological data (Q99165) (← links)
- The variant call format and VCFtools (Q99352) (← links)
- Pooled variable scaling for cluster analysis (Q100788) (← links)
- Reliable ABC model choice via random forests (Q100825) (← links)
- ABC random forests for Bayesian parameter inference (Q100827) (← links)
- A robust AMMI model for the analysis of genotype-by-environment data (Q101491) (← links)
- mlr3proba: an R package for machine learning in survival analysis (Q101706) (← links)
- Estimating and testing high-dimensional mediation effects in epigenetic studies (Q101726) (← links)
- IMIX: a multivariate mixture model approach to association analysis through multi-omics data integration (Q101976) (← links)
- tqDist: a library for computing the quartet and triplet distances between binary or general trees (Q103567) (← links)
- Fast and interpretable genomic data analysis using multiple approximate kernel learning (Q103688) (← links)
- GHap: an R package for genome-wide haplotyping (Q104041) (← links)
- Inferring clonal heterogeneity in cancer using SNP arrays and whole genome sequencing (Q104107) (← links)
- Mercator: a pipeline for multi-method, unsupervised visualization and distance generation (Q104132) (← links)
- HUM calculator and HUM package for R: easy-to-use software tools for multicategory receiver operating characteristic analysis (Q104931) (← links)
- CePa: an R package for finding significant pathways weighted by multiple network centralities (Q105752) (← links)
- bdvis: visualizing biodiversity data in R (Q105869) (← links)
- Model-based clustering of microarray expression data via latent Gaussian mixture models (Q107981) (← links)
- GEInter: an R package for robust gene–environment interaction analysis (Q108199) (← links)
- Statistical significance based on length and position of the local score in a model of i.i.d. sequences (Q108492) (← links)
- circlize implements and enhances circular visualization in R (Q109067) (← links)
- DIME: R-package for identifying differential ChIP-seq based on an ensemble of mixture models (Q109222) (← links)
- integIRTy: a method to identify genes altered in cancer by accounting for multiple mechanisms of regulation using item response theory (Q109781) (← links)
- SIBER: systematic identification of bimodally expressed genes using RNAseq data (Q109815) (← links)
- RMTL: an R library for multi-task learning (Q109895) (← links)
- GGRaSP: a R-package for selecting representative genomes using Gaussian mixture models (Q110817) (← links)
- influx_s: increasing numerical stability and precision for metabolic flux analysis in isotope labelling experiments (Q111368) (← links)
- A novel signaling pathway impact analysis (Q111381) (← links)
- CINNA: an R/CRAN package to decipher Central Informative Nodes in Network Analysis (Q111657) (← links)
- Amanida: an R package for meta-analysis of metabolomics non-integral data (Q112075) (← links)
- MALDIrppa: quality control and robust analysis for mass spectrometry data (Q112174) (← links)
- MOSS: multi-omic integration with sparse value decomposition (Q112390) (← links)
- MixTwice: large-scale hypothesis testing for peptide arrays by variance mixing (Q113843) (← links)
- Detecting quantitative trait loci and exploring chromosomal pairing in autopolyploids using polyqtlR (Q115560) (← links)
- Unsupervised multiple kernel learning for heterogeneous data integration (Q116481) (← links)
