Aufiero / circRNAprofilerLinks
☆10Updated last month
Alternatives and similar repositories for circRNAprofiler
Users that are interested in circRNAprofiler are comparing it to the libraries listed below
Sorting:
- West Coast Dream Team Whole Genome Bisulfite Sequencing☆15Updated 4 years ago
- scripts for the integrating ATAC-seq, RNA-seq and CHi-C paper☆24Updated 2 years ago
- R package to calculate the Aneuploidy Score from Chromosome Arm-level SCNAs/Aneuploidies (CAAs) as outlined and expanded by Shukla et al.…☆16Updated 4 years ago
- ☆17Updated 4 years ago
- GENome Organisation Visual Analytics☆15Updated 3 years ago
- Main repository for Drews et al. (Nature, 2022)☆42Updated last year
- Analysis pipeline for our circSC manuscript☆13Updated 3 years ago
- CNV analysis workflow code for the manuscript☆13Updated 5 years ago
- ORF Quantification pipeline for Alternative Splicing☆16Updated 4 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
- ☆23Updated 4 years ago
- A R script to perform clustering of gene expression time-series RNA-seq data with Mfuzz.☆20Updated 6 years ago
- Process m6A/MeRIP-seq data in a single or batch job mode☆20Updated 5 years ago
- Somatic coding and non-coding mutation enrichment analysis for tumor WGS data☆11Updated 4 years ago
- ☆28Updated 6 months ago
- ☆25Updated last year
- Scripts used for the ACT paper☆12Updated 4 years ago
- ☆9Updated 5 years ago
- CNApp represents the first web tool to perform a comprehensive and integrative analysis of copy number alterations (CNAs) in a user-frien…☆20Updated 5 years ago
- Detection of differential translated genes using Ribo-seq☆16Updated 4 years ago
- MAnorm2 for Normalizing and Comparing ChIP-seq Samples☆33Updated 2 years ago
- A multi-method comparative bioinformatics pipeline to detect and study circRNAs from RNA-seq data☆15Updated 5 years ago
- ☆21Updated 3 months ago
- A flexible framework to annotate and prioritize cancer somatic mutations.☆8Updated 8 years ago
- Advanced plotting functions for CNV data generated by CNV-Seq and Control Freec☆13Updated 4 years ago
- ☆17Updated 11 months ago
- ☆17Updated 6 years ago
- Abismal is a mapper of FASTQ bisulfite-converted short reads (between 50 and 1000 bases) to a FASTA reference genome.☆18Updated last week
- A tool kit for dissecting cancer evolution from multi-region derived tumor biopsies via somatic mutations☆36Updated 3 years ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Updated 6 years ago