daisybio / TF-PrioritizerLinks
Bioinformatics pipeline to identify differentially active transcription factors between conditions using expression and epigenetic data
☆14Updated last year
Alternatives and similar repositories for TF-Prioritizer
Users that are interested in TF-Prioritizer are comparing it to the libraries listed below
Sorting:
- The Zavolab Automated RNA-seq Pipeline☆36Updated 4 months ago
- Junction centric alternative splicing translator☆21Updated 3 years ago
- An R package for finding non-adenosine residues in poly(A) tails of ONT direct RNA sequencing reads☆13Updated last month
- interactive plots for differential expression analysis☆34Updated 5 months ago
- nRex: Germline and somatic single-nucleotide, short indel and structural variant calling☆12Updated 2 months ago
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆36Updated last year
- rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysis☆63Updated 6 months ago
- Frequently used commands in Bioinformatics☆21Updated 2 months ago
- a metabologenomic pipeline integrating metabolomic and genomic data to identify novel RiPPs and their BGCs☆12Updated 4 years ago
- ☆33Updated 3 weeks ago
- Millefy: Genome browser-like visualization of single-cell RNA-seq dataset☆29Updated 5 years ago
- Merge fastq files split over lanes☆20Updated 7 years ago
- Test data for MultiQC.☆22Updated this week
- An R interface to the MEME Suite☆53Updated 5 months ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆56Updated last week
- for visual evaluation of read support for structural variation☆55Updated last year
- A nextflow pipeline which integrates multiple omic data streams and performs coordinated analysis☆11Updated last year
- deepStats: a stastitical toolbox for deeptools and genomic signals☆35Updated 4 years ago
- Prepare Sailfish and Salmon output for downstream analysis☆42Updated 6 years ago
- A bioinformatics pipeline for viral transcriptome detection and quantification considering splicing.☆36Updated 3 years ago
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆44Updated this week
- Introme prioritises coding and noncoding splice-altering variants for clinical variant interpretation☆21Updated last week
- Snakemake pipeline for running MAJIQ☆23Updated last year
- LongcallR is a SNP caller for single molecule long-read RNA-seq data☆69Updated this week
- Slinker offers a succinct and complementary method to visualise RNA-Seq data through superTranscripts.☆19Updated 3 years ago
- visual analysis of your VCF files☆38Updated 3 years ago
- Useful tools for working with Salmon output☆39Updated 5 years ago
- A script to make downloading of SRA/GEO data easier☆31Updated 2 years ago
- ☆34Updated 3 weeks ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago