LappalainenLab / lorals_paper_codeLinks
☆27Updated 3 years ago
Alternatives and similar repositories for lorals_paper_code
Users that are interested in lorals_paper_code are comparing it to the libraries listed below
Sorting:
- ☆18Updated last year
- ☆38Updated 2 years ago
- The cattle Genotype-Tissue Expression atlas v1☆28Updated 2 years ago
- ☆20Updated 3 years ago
- TEProf2 Pipeline used to find promoters and predict protein sequences from RNA-sequencing data☆27Updated 2 years ago
- ☆37Updated 6 years ago
- Improving gene isoform quantification with miniQuant☆29Updated 2 months ago
- Summarise and plot data from long-read ONT (direct RNA/cDNA) BAM files☆15Updated last year
- The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVOR…☆32Updated last year
- A pipeline for identifying conserved topologically associating domain boundaries among multiple species.☆16Updated 5 months ago
- Hi-C Interaction Frequency Inference (HIFI): High-resolution estimation of DNA-DNA interaction frequency from Hi-C data☆24Updated 3 years ago
- ☆18Updated last year
- ☆17Updated 5 years ago
- Long-read Isoform Quantification and Analysis☆38Updated 8 months ago
- ExOrthist: a pipeline to extract exon orthologies at any evolutionary distance.☆25Updated last year
- Identify and annotate TE-mediated insertions in long-read sequence data☆46Updated 5 months ago
- “When everything is connected to everything else, for better or worse, everything matters.” Bruce Mau☆19Updated 5 years ago
- ☆24Updated 11 months ago
- A comprehensive pipeline for RNAseq data analysis☆22Updated last year
- ☆22Updated 2 years ago
- An R package for performing MetaSTAAR procedure in whole-genome sequencing studies☆25Updated last year
- LongcallR is a SNP caller for single molecule long-read RNA-seq data☆69Updated this week
- R package to explore active transposable elements with RNA-seq data☆21Updated 3 years ago
- A graph-based pipeline used to call/genotype snvs/indels/SVs from NGS data☆16Updated 3 months ago
- ☆16Updated 3 years ago
- Pipeline to identify isoforms from full-length cDNA sequencing data☆25Updated 2 months ago
- Analysis of gene expression and splicing diversity in a subset of samples from the 1000 Genomes Project, including eQTL and sQTL discover…☆42Updated last year
- Micro DNA identification☆24Updated 4 years ago
- ☆20Updated 2 years ago
- FINSURF is a tool designed to analyse lists of sequences variants in the human genome.☆12Updated 3 years ago