hms-dbmi / exac_browser
Browser for ExAC consortium data
☆12Updated 7 years ago
Alternatives and similar repositories for exac_browser:
Users that are interested in exac_browser are comparing it to the libraries listed below
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 3 years ago
- utilities for working with IGV: opening files remotely in either desktop IGV or a web viewer (igv.js), creating screenshots, etc.☆48Updated 5 years ago
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆33Updated 7 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 4 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated last month
- create a gemini-compatible database from a VCF☆56Updated 4 years ago
- filtering trio-based genetic variants in VCFs for clinical review☆21Updated 4 years ago
- Analysis from kallisto paper☆32Updated 8 years ago
- ☆24Updated 8 months ago
- JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes☆22Updated 3 weeks ago
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆16Updated 8 months ago
- ☆21Updated this week
- Tip and tricks for VCF files☆21Updated 6 years ago
- Generic human DNA variant annotation pipeline☆57Updated 11 months ago
- Analysis for svaseq paper☆19Updated 10 years ago
- Fork of https://code.google.com/p/ngs-analysis☆18Updated 11 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆10Updated 5 years ago
- ☆26Updated 6 years ago
- ☆30Updated 3 years ago
- 3D hotspot mutation proximity analysis tool☆46Updated last year
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated last year
- Code associated with 2019 manuscript entitled "Transcript expression-aware annotation improves rare variant discovery and interpretation…☆33Updated 2 years ago
- ☆23Updated last month
- An awk-like VCF parser☆55Updated last year
- Rna-seq pipeline, From FASTQ to differential expression analysis...☆20Updated 7 years ago
- a wee tool for random access into BGZF files.☆84Updated 6 years ago
- RNA-Seq Snakemake example with Jekyll homepage creation☆20Updated 10 years ago
- ☆68Updated 2 years ago
- Convert, explore, and manipulate GFF and GTF files (used in bioinformatics) using a sqlite-based approach☆35Updated 14 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 4 years ago