Augroup / miniQuantLinks
Improving gene isoform quantification with miniQuant
☆23Updated 2 weeks ago
Alternatives and similar repositories for miniQuant
Users that are interested in miniQuant are comparing it to the libraries listed below
Sorting:
- Identify and annotate TE-mediated insertions in long-read sequence data☆42Updated last week
- ☆19Updated 2 years ago
- ExOrthist: a pipeline to extract exon orthologies at any evolutionary distance.☆25Updated 7 months ago
- LongcallR is a SNP caller for single molecule long-read RNA-seq data☆62Updated 2 weeks ago
- ☆36Updated 2 years ago
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆24Updated 10 months ago
- A pipeline to detect chimeric transcripts derived from genes and transposable elements.☆30Updated 2 months ago
- ☆26Updated 3 years ago
- Hi-C Interaction Frequency Inference (HIFI): High-resolution estimation of DNA-DNA interaction frequency from Hi-C data☆24Updated 2 years ago
- ☆23Updated 6 months ago
- Long-read Isoform Quantification and Analysis☆38Updated 3 months ago
- ☆33Updated last year
- Pipeline to identify isoforms from full-length cDNA sequencing data☆25Updated 2 months ago
- TEMP is a software package for detecting transposable elements (TEs) insertions and excisions from pooled high-throughput sequencing dat…☆22Updated 7 years ago
- ☆37Updated 5 years ago
- Summarise and plot data from long-read ONT (direct RNA/cDNA) BAM files☆14Updated last year
- Simple library/pipeline to generate and handle Hi-C data.☆38Updated 7 months ago
- Invertory of TE-gene isoforms☆11Updated last year
- Split-read pipeline for the identification of non-reference TE insertions with TSDs☆25Updated 4 years ago
- ☆19Updated 11 months ago
- ☆16Updated 4 years ago
- An accurate repeat detection from Nanopore data using deep learning and image techniques☆22Updated 2 years ago
- ERVcaller is a tool designed to accurately detect and genotype non-reference unfixed endogenous retroviruses (ERVs) and other transposabl…☆13Updated last year
- GENE-SWitCH project RNA-Seq analysis pipeline☆28Updated 4 months ago
- SQANTI2 is now replaced by SQANTI3. Please go to: https://github.com/ConesaLab/SQANTI3☆38Updated 5 years ago
- Easy genomic regions for short-read variant calling☆30Updated this week
- R package to explore active transposable elements with RNA-seq data☆20Updated 2 years ago
- Scoring GT/AG sites for improving spliced alignment☆45Updated this week
- microRNA PREdiction From small RNA-seq data☆29Updated 7 years ago
- EM based transcript abundance from nanopore reads mapped to a transcriptome with minimap2☆61Updated 9 months ago