nanoporetech / dRNA-paper-scriptsLinks
Direct RNA publication scripts
☆11Updated 7 years ago
Alternatives and similar repositories for dRNA-paper-scripts
Users that are interested in dRNA-paper-scripts are comparing it to the libraries listed below
Sorting:
- Code associated with the manuscript "A complete reference genome improves analysis of human genetic variation".☆17Updated 2 years ago
- toolkit to process gtf files☆17Updated 3 years ago
- ☆13Updated 2 years ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 4 months ago
- Pipeline for eukaryotic genome annotation based on external evidences☆13Updated 2 years ago
- All kinds of NGS analysis pipeline☆12Updated 5 years ago
- ☆15Updated last year
- Split-read pipeline for the identification of non-reference TE insertions with TSDs☆25Updated 4 years ago
- FastRemap, a C++ tool for quickly remapping reads between genome assemblies based on the commonly used CrossMap tool. Link to paper: http…☆26Updated 3 years ago
- Repository for pipeline code☆26Updated last year
- CNEFinder: Finding Conserved Non-coding Elements in Genomes☆24Updated 4 years ago
- Code used to process and analyze structural variants and short tandem repeat variants profiled in 719 deeply sequenced whole genomes as p…☆11Updated 6 years ago
- ☆10Updated last year
- ☆19Updated 2 years ago
- Enabling differential allele-specific analysis☆11Updated 8 months ago
- ☆10Updated 3 years ago
- ☆27Updated 2 years ago
- This is the Haplotypo repository☆20Updated last year
- A software suite for accurate identification, annotation, translation, and feature characterization of annotate transcripts.☆19Updated 3 years ago
- Invertory of TE-gene isoforms☆11Updated last year
- Long Read Based SV Calling Tools Analysis☆14Updated last year
- TideHunter: efficient and sensitive tandem repeat detection from noisy long reads using seed-and-chain☆20Updated last year
- Scripts to do haplotype analysis on pan genomes.☆21Updated 4 years ago
- This is a basic repository with all the scripts necessary to reconstruct the data analysis from our work on the 200 Genomes☆11Updated 6 years ago
- Scripts and files used in the generation of the COLO829 somatic SV truthset.☆13Updated 3 years ago
- Repository☆10Updated 10 months ago
- ☆31Updated last year
- Codes for the Iso-Seq variant-calling paper☆11Updated 2 years ago
- Plot allele frequencies in VCF files☆11Updated 6 years ago
- I often use some of the self-written programs.☆16Updated 5 months ago