furkanmtorun / gnomad_python_apiLinks
[deprecated] 🧬 Python API to fetch gnomAD data
☆22Updated 3 years ago
Alternatives and similar repositories for gnomad_python_api
Users that are interested in gnomad_python_api are comparing it to the libraries listed below
Sorting:
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆83Updated last month
- ☆39Updated 2 weeks ago
- Website to analyze conflicting assertions in ClinVar☆18Updated last year
- Python package to annotate and visualize gene fusions.☆63Updated 9 months ago
- A guide to running MaxQuant in Linux☆33Updated 5 years ago
- Tissue-specific variant effect predictions on splicing☆42Updated 2 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆47Updated this week
- BEAVR: A Browser-based tool for the Exploration And Visualization of RNAseq data☆25Updated 3 years ago
- Tools for making plots of genomic datasets in a genome-browser-like format☆32Updated 7 months ago
- A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.☆46Updated 2 years ago
- A webtool for the clinical interpretation of CNVs in rare disease patients☆12Updated 3 years ago
- Clinical interpretation of somatic mutations in cancer☆47Updated 4 months ago
- VEP Plugin to annotate high-impact five prime UTR variants☆27Updated 10 months ago
- B-cell and T-cell Adaptive Immune Receptor Repertoire (AIRR) sequencing analysis pipeline using the Immcantation framework☆64Updated last week
- ☆21Updated 3 months ago
- JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes☆23Updated 6 months ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆49Updated 4 years ago
- Gene Fusion Visualiser☆51Updated 2 years ago
- CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data.☆39Updated 2 months ago
- Robust, tested workflows for RNA-seq, ChIP-seq and other high-throughput sequencing analysis☆23Updated this week
- predicts neoepitopes from phased somatic mutations detected using tumor/normal DNA-seq data☆27Updated last year
- Builds a PEP from SRA or GEO accessions☆52Updated this week
- The Zavolab Automated RNA-seq Pipeline☆35Updated this week
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆28Updated 2 years ago
- Analysis pipeline for the GUIDE-seq assay.☆26Updated 2 months ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆41Updated last year
- A BioWDL pipeline for processing RNA-seq data, starting with FASTQ files to produce expression measures and VCFs. Category:Multi-Sample☆32Updated 2 years ago
- Toolkit for benchmarking fusion transcript predictions☆19Updated 10 months ago
- Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products☆36Updated 3 weeks ago