vidboda / MobiDetails
WebApp for DNA variants interpretation
☆13Updated last week
Alternatives and similar repositories for MobiDetails:
Users that are interested in MobiDetails are comparing it to the libraries listed below
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- filtering trio-based genetic variants in VCFs for clinical review☆21Updated 4 years ago
- robust matching of small variant datasets using flexible scoring schemes☆10Updated 5 years ago
- The OpEx (Optimised Exome) pipeline☆9Updated 6 years ago
- ☆21Updated 2 weeks ago
- Samwell: a python package for using genomic files... well☆20Updated 2 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆21Updated 3 years ago
- Opossum is a tool to pre-process RNA-seq reads prior to variant calling.☆28Updated 6 years ago
- Universal RObust Peak Annotator☆15Updated last year
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Updated 7 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated 8 months ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 5 years ago
- Structural Variation breakpoint discovery via adaptive learning☆15Updated last year
- This BLENDER has been sunsetted☆16Updated 6 months ago
- vgraph is a command line application and Python library to compare genetic variants using variant graphs. ``vgraph`` utilizes a graph re…☆43Updated 3 years ago
- This repository contains Jupyter Notebooks containing GATK Best Practices Workflows☆26Updated 5 years ago
- nRex: Germline and somatic single-nucleotide, short indel and structural variant calling☆12Updated this week
- The Loss-of-Function ToolKit (LoFTK) allows efficient and automated prediction of LoF variants from both genotyped and sequenced genomes,…☆9Updated 3 weeks ago
- Generic human DNA variant annotation pipeline☆58Updated last year
- A Feature Density Estimator for High-Throughput Sequence Tags☆23Updated 3 years ago
- Mutation Identification Pipeline. Read the latest documentation:☆44Updated last year
- GenoTypes Compressor☆15Updated 2 years ago
- PGxPOP☆16Updated 2 years ago
- Simplify snpEff annotations for interesting cases☆21Updated 6 years ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆32Updated last year
- Aggregation and analyses of rare CNVs across diseases☆14Updated 2 years ago
- Support code for NGS copy number algorithms. Takes a file of locations and a [cr|b]am file and generates a count of coverage of each alle…☆44Updated 2 years ago
- Linking GWAS studies to genes through cis-regulatory datasets☆39Updated 2 years ago
- Repo for downloading and storing OMIM data☆19Updated 8 years ago