NVIDIA-Genomics-Research / DL4VCLinks
☆11Updated 5 years ago
Alternatives and similar repositories for DL4VC
Users that are interested in DL4VC are comparing it to the libraries listed below
Sorting:
- Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/☆45Updated 2 years ago
- ☆23Updated 6 years ago
- Documenting usage and experience with bioinformatic tools☆40Updated 9 years ago
- ☆68Updated 2 years ago
- Read visualizer for structural variants☆84Updated 6 years ago
- Method for detecting STR expansions from short-read sequencing data☆63Updated 3 years ago
- FInding REliable Variants without ArTifacts☆22Updated 2 years ago
- Arioc: GPU-accelerated DNA short-read alignment☆70Updated 2 weeks ago
- utilities for working with IGV: opening files remotely in either desktop IGV or a web viewer (igv.js), creating screenshots, etc.☆49Updated 6 years ago
- GEM-Mapper v3☆58Updated 2 months ago
- for visual evaluation of read support for structural variation☆54Updated last year
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- Aligner for sequencing data☆21Updated 9 years ago
- Data and information about the Polaris study☆53Updated 5 years ago
- Somatic copy number analysis using WGS paired end wholegenome sequencing☆71Updated 4 years ago
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆98Updated 2 years ago
- A new workflow for the custom design of CRISPR libraries.☆21Updated 2 years ago
- ☆82Updated 3 years ago
- 3D hotspot mutation proximity analysis tool☆47Updated 2 years ago
- Generic human DNA variant annotation pipeline☆58Updated last year
- Assembly Based ReAligner☆73Updated 7 years ago
- ☆46Updated 5 years ago
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 4 years ago
- Very simple, pure python, BAM file reader☆79Updated 6 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆65Updated last year
- Battenberg algorithm and associated implementation script☆52Updated 4 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆24Updated 3 months ago
- Remove primer sequence from BAM alignments by soft-clipping☆31Updated 5 years ago
- ☆53Updated 4 years ago
- DEPRECATED. This tool has been superseded by https://github.com/griffithlab/pVACtools☆61Updated 6 years ago