epam / NGBLinks
New Genome Browser (NGB) - a Web - based NGS data viewer with unique Structural Variations (SVs) visualization capabilities, high performance, scalability, and cloud data support
☆165Updated 3 months ago
Alternatives and similar repositories for NGB
Users that are interested in NGB are comparing it to the libraries listed below
Sorting:
- A collection of reusable WDL tasks. Category:Other☆88Updated 3 months ago
- Documentation and description of AWS iGenomes S3 resource.☆117Updated 11 months ago
- Sequana: a set of Snakemake NGS pipelines☆149Updated last week
- Extensible specification for representing and uniquely identifying biological sequence variation☆94Updated last month
- VarDict Java port☆136Updated last year
- The nimble & robust variant annotator☆186Updated last year
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆91Updated 2 months ago
- A tool set for short variant discovery in genetic sequence data.☆202Updated 4 years ago
- TransVar - multiway annotator for precision medicine☆126Updated 2 years ago
- Open workflow definitions for genomic analysis from MGI at WUSM.☆105Updated 4 months ago
- HTML5 scrollable genome browser☆111Updated 2 years ago
- A modular annotation tool for genomic variants☆137Updated this week
- Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing☆133Updated 5 years ago
- Simple FASTQ quality assessment using Python☆108Updated 4 years ago
- VarSim: A high-fidelity simulation validation framework for high-throughput genome sequencing with cancer applications☆90Updated last year
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆128Updated 5 years ago
- This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…☆128Updated 5 years ago
- Tools for manipulating biological data, particularly multiple sequence alignments☆158Updated 2 weeks ago
- GATK RNA-Seq Variant Calling in Nextflow☆137Updated 2 years ago
- Extension for Jupyter which integrates igv.js☆154Updated 2 years ago
- Example Nextflow pipelines and programming techniques☆106Updated last month
- ABRA2☆95Updated 2 years ago
- Biopieces is a bioinformatic framework of tools easily used and easily created.☆143Updated 7 years ago
- All source code of the crispor.org website☆82Updated 2 months ago
- C++ Library to parse Illumina InterOp files☆79Updated 5 months ago
- Very simple, pure python, BAM file reader☆79Updated 6 years ago
- This repository contains information about latest release from Genome in a Bottle project☆75Updated 6 years ago
- ☆184Updated 2 years ago
- Plugins for the Ensembl Variant Effect Predictor (VEP)☆161Updated last month
- NEAT read simulation tools☆101Updated 3 years ago