seandavi / MachineLearningIntroLinks
Machine learning use cases for teaching
☆13Updated 8 years ago
Alternatives and similar repositories for MachineLearningIntro
Users that are interested in MachineLearningIntro are comparing it to the libraries listed below
Sorting:
- RNA-seq quantifications: gene expression responses to human rhinovirus infection for 6 asthmatic and 6 non-asthmatic donors (SRP046226)☆19Updated 8 years ago
- ☆10Updated 6 years ago
- Targeted and non-targeted anticancer drugs and drug regimens☆29Updated last week
- R Interface to the NCBI SRA metadata☆23Updated 7 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- Repository for signature genes from Immune Cell Atlas☆18Updated 6 years ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- ☆12Updated last year
- R interface to megadepth: BigWig and BAM related utilities☆12Updated last year
- TOP results by CONfident efFECT Sizes.☆15Updated last year
- TFregulomeR reveals transcription factors’ context-specific features and functions☆15Updated 3 years ago
- Bioconductor2017 workshop - Analysis of single-cell RNA-seq data: Normalization, dimensionality reduction, clustering, and lineage infere…☆11Updated 8 years ago
- R/BioC package to estimate the cell composition of whole blood in DNA methylation samples in microarray or sequencing platforms☆18Updated 3 weeks ago
- Extracting mutational signatures via LASSO. The manuscript of the method is published on PLOS Computational Biology and available at: htt…☆11Updated 2 months ago
- Molecular Signatures Database (MSigDB) in a data frame☆16Updated 7 years ago
- A Practical (And Opinionated) Guide To Analyzing 450K Data☆35Updated 11 years ago
- Examples of kallisto + sleuth☆11Updated 8 years ago
- zero-inflated negative binomial gene expression in R☆20Updated 7 years ago
- A set of tools for accurate quantitation of single-cell allele-specific expression☆13Updated 2 years ago
- ☆12Updated last month
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆14Updated 4 years ago
- Workflow for ZINB-WaVE + DESeq2 intergration for single-cell RNA-seq☆30Updated 4 years ago
- R wrapper for utilizing the SigProfilerMatrixGenerator framework☆20Updated 2 years ago
- Interactive benchmarking of ranking and assignment methods☆16Updated last week
- Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R☆32Updated 2 months ago
- R package to organise and standardise your genomic variant calls obtained with different callers.☆11Updated 6 years ago
- 🧭 Navigate single-cell RNA-seq datasets in your web browser.☆29Updated 2 years ago
- This repository contains the code to run the ASCETS arm-level copy number events caller for targeted sequencing data. ASCETS produces arm…☆18Updated last year
- mitochondrial variant analysis tools☆15Updated 4 years ago
- integrative pathway analysis with modern PCA methodology and gene selection☆11Updated 2 years ago