vidboda / MobiDetailsLinks
WebApp for DNA variants interpretation
☆14Updated this week
Alternatives and similar repositories for MobiDetails
Users that are interested in MobiDetails are comparing it to the libraries listed below
Sorting:
- ☆21Updated last month
- filtering trio-based genetic variants in VCFs for clinical review☆21Updated 5 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- This repository contains Jupyter Notebooks containing GATK Best Practices Workflows☆26Updated 5 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆30Updated 4 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Updated 3 years ago
- variant integration methods for the 1000 Genomes Project☆21Updated 7 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- Generic human DNA variant annotation pipeline☆58Updated last year
- (WIP) best-practices workflow for rare disease☆62Updated last year
- Website to analyze conflicting assertions in ClinVar☆18Updated last year
- Distributed execution of bioinformatics tools on Apache Spark. Apache 2 licensed.☆41Updated 6 months ago
- Simple vcf parser, based on PyVCF☆46Updated 6 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 9 months ago
- vgraph is a command line application and Python library to compare genetic variants using variant graphs. ``vgraph`` utilizes a graph re…☆43Updated 4 years ago
- Fast spliced aligner with low memory requirements☆41Updated 10 years ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆33Updated 2 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 7 months ago
- Copy Number Methods for Detection and Genome Wide Association Tests☆22Updated 10 months ago
- Genomic VCF to tab-separated values☆47Updated 2 years ago
- Genome-wide imputation pipeline☆31Updated last year
- conda recipes for genomic data☆84Updated 4 years ago
- An automated RNA-seq pipeline using Nextflow☆37Updated last year
- Sparse Project VCF: evolution of VCF to encode population genotype matrices efficiently☆58Updated last year
- Remove primer sequence from BAM alignments by soft-clipping☆31Updated 5 years ago
- Calling star alleles in highly polymorphic pharmacogenes (e.g. CYP450 genes) by leveraging genome graph-based variant detection.☆34Updated last week
- Sanity check Variant Call Format (VCF) files.☆37Updated 9 years ago
- A simple variant calling and annotation pipeline using BWA, GATK and ENSEMBL. This version of the pipeline uses the Rubra/Ruffus framewor…☆34Updated 11 years ago
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆75Updated last month