DiogoVeiga / maserLinks
Mapping Alternative Splicing Events to pRoteins
☆20Updated 3 years ago
Alternatives and similar repositories for maser
Users that are interested in maser are comparing it to the libraries listed below
Sorting:
- Filtering of PDX samples for mouse derived reads☆28Updated 2 years ago
- R package with motifs for use with chromVAR☆28Updated 7 years ago
- Pipeline to analyze long-read mRNA isoforms and ORF products sequenced in breast cancer using PacBio Single-Molecule technology.☆16Updated 3 years ago
- Explore the cancer relevance of your gene list☆52Updated 2 weeks ago
- Harvard FAS informatics scRNAseq workshop website☆38Updated 6 years ago
- Algorithm for detecting alternative splicing in a population of single cells. See details in Welch et al., Nucleic Acids Research 2016: h…☆22Updated 9 years ago
- Machine learning algorithm to predict biological pathway relationships based on functional genomics networks☆20Updated 7 years ago
- processes GoT amplicon data and generates a table of metrics☆32Updated 3 years ago
- Discover differential transcript usage from polyA-captured single cell RNA-seq data☆51Updated 2 years ago
- Snakemake pipeline for benchmarking cell-type deconvolution methods and deconvolving real bulk RNA-seq data with the use of scRNA-seq dat…☆15Updated 5 months ago
- ☆23Updated last year
- Snakemake pipeline for running MAJIQ☆23Updated last year
- MAnorm2 for Normalizing and Comparing ChIP-seq Samples☆32Updated 2 years ago
- Bead-based single-cell atac processing☆33Updated 3 years ago
- ☆24Updated 4 months ago
- ☆44Updated 6 years ago
- Lightweight Iterative Gene set Enrichment in R☆57Updated last year
- Model-based tumour subclonal deconvolution using population genetics☆33Updated last month
- An R package to analyze single-cell V(D)J data☆28Updated last year
- Collection of functions created and/or curated to aid in the visualization and analysis of single-cell data using R.☆16Updated 3 years ago
- ☆28Updated last year
- An R package for studying mutational signatures and structural variant signatures along clonal evolution in cancer.☆71Updated last year
- Code accompanying Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes☆44Updated 4 years ago
- Identify and correct invalid gene symbols☆59Updated 10 months ago
- SCASA: Single cell transcript quantification tool☆21Updated last year
- CONICS: COpy-Number analysis In single-Cell RNA-Sequencing☆75Updated 2 years ago
- R vignettes for processing BUS format single-cell RNA-seq files☆20Updated 5 years ago
- A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites.☆29Updated last year
- Software Package for Transcription Factor Binding Site (TFBS) Analysis☆30Updated 6 months ago
- Interactive R package to quantify, analyse and visualise alternative splicing☆37Updated this week