cobilab / cryfaLinks
A secure encryption tool for genomic data
☆62Updated last year
Alternatives and similar repositories for cryfa
Users that are interested in cryfa are comparing it to the libraries listed below
Sorting:
- Sparse Project VCF: evolution of VCF to encode population genotype matrices efficiently☆59Updated 2 years ago
- software tool for the manipulation, annotation, selection, and analysis of variants in the context of next-gen sequencing analysis☆30Updated 4 years ago
- Julia package powering VIVA, our tool for visualization of genomic variation data. Manual:☆87Updated 2 years ago
- HPG Aligner is an ultrafast and highly sensitive Next-Generation Sequencing (NGS) mapper which supoprts both DNA and RNA alignment☆34Updated 8 years ago
- Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; a…☆71Updated this week
- A modular annotation tool for genomic variants☆146Updated last week
- Workflows for germline short variant discovery in WGS data. PairedEndSingleSampleWf has been superseded in Broad production by https://gi…☆57Updated 5 years ago
- small RNA analysis from NGS data☆38Updated last year
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- Genomic VCF to tab-separated values☆48Updated 2 years ago
- Thousand Variant Callers Project Repository☆73Updated 6 years ago
- Scallop is a reference-based transcriptome assembler for RNA-seq☆92Updated 4 years ago
- Cancer Predisposition Sequencing Reporter (CPSR)☆63Updated 3 months ago
- Generic human DNA variant annotation pipeline☆59Updated last year
- ☆96Updated 3 years ago
- A Snakemake workflow for calling small and structural variants under any kind of scenario (tumor/normal, tumor/normal/relapse, germline, …☆88Updated this week
- Arioc: GPU-accelerated DNA short-read alignment☆70Updated 8 months ago
- TIDDIT - structural variant calling☆78Updated 2 months ago
- Method for detecting STR expansions from short-read sequencing data☆63Updated 4 years ago
- Fast fusion detection using kallisto☆79Updated 7 months ago
- RUFUS k-mer based genomic variant detection☆54Updated last month
- (WIP) best-practices workflow for rare disease☆62Updated last year
- WDL’s and Dockerfiles for assembly QC process☆72Updated 6 months ago
- Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/☆48Updated 5 months ago
- A collection of publications on comparison of high-throughput sequencing technologies.☆27Updated 2 months ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆64Updated last week
- Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes☆67Updated last month
- ☆55Updated 5 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆59Updated 8 years ago
- My bioinfo toolbox☆50Updated last year