PacificBiosciences / DevNet
The DevNet project on github stores the PacBio DevNet website.
☆116Updated 6 years ago
Alternatives and similar repositories for DevNet
Users that are interested in DevNet are comparing it to the libraries listed below
Sorting:
- VarDict☆199Updated last year
- pbsv - PacBio structural variant (SV) calling and analysis tools☆145Updated 2 months ago
- SV detection from paired end reads mapping☆117Updated 5 years ago
- Variant calling and somatic mutation/CNV detection for next-generation sequencing data☆158Updated 2 years ago
- Nextflow pipeline for analysis of direct RNA Nanopore reads☆102Updated 2 weeks ago
- ☆120Updated 6 months ago
- BAM Statistics, Feature Counting and Annotation☆149Updated 3 months ago
- Tool for stripping adaptors and/or merging paired reads with overlap into single reads.☆143Updated 8 years ago
- Whole Genome Simulator for Next-Generation Sequencing☆97Updated 5 months ago
- Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data☆114Updated 3 years ago
- Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics☆110Updated 3 weeks ago
- Same species annotation lift over pipeline.☆97Updated last year
- Relevant papers for CNV and SV approaches☆94Updated 6 months ago
- PacBio Assembly Tool Suite: Reads in ⇨ Assembly out☆117Updated 4 years ago
- A tool to identify, orient, trim and rescue full length cDNA reads☆81Updated 2 years ago
- Bayesian genotyper for structural variants☆132Updated 4 years ago
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆101Updated 4 years ago
- FEELnc : FlExible Extraction of LncRNA☆87Updated 8 months ago
- Script to automatically create and run IGV snapshot batchscripts☆141Updated 2 years ago
- ABRA2☆92Updated 2 years ago
- NEAT read simulation tools☆98Updated 2 years ago
- Read visualizer for structural variants☆83Updated 6 years ago
- This repository contains information about latest release from Genome in a Bottle project☆74Updated 5 years ago
- A tool for profiling long STRs from short reads☆96Updated 4 years ago
- A structural variation pipeline for short-read sequencing☆187Updated last week
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆98Updated 2 years ago
- ☆124Updated this week
- Snakemake pipelines for nanopore sequencing data archiving and processing☆90Updated 3 years ago
- Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data☆159Updated 8 months ago
- phasing and Allele Specific Expression from RNA-seq☆114Updated 10 months ago