cobilab / cryfa
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:
- Fast fusion detection using kallisto☆80Updated 6 months ago
- (WIP) best-practices workflow for rare disease☆60Updated 10 months ago
- A collection of publications on comparison of high-throughput sequencing technologies.☆27Updated 4 months ago
- Sparse Project VCF: evolution of VCF to encode population genotype matrices efficiently☆58Updated last year
- RNA-Seq Mutation Detection☆28Updated 3 years ago
- An efficient index for the colored, compacted, de Bruijn graph☆110Updated 7 months ago
- List of IARC bioinformatics nextflow pipelines☆51Updated 4 months ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆66Updated 2 years ago
- Cancer Predisposition Sequencing Reporter (CPSR)☆59Updated last month
- Scallop is a reference-based transcriptome assembler for RNA-seq☆90Updated 4 years ago
- small RNA analysis from NGS data☆37Updated 8 months ago
- pipeline for the analysis of small RNA data☆14Updated 5 years ago
- Long-read splice alignment with high accuracy☆63Updated 7 months ago
- igv.js standalone page generator and automatic configuration to view bam/cram/vcf/bed. "working in under 1 minute"☆127Updated last year
- A bit-packed k-mer representation (and relevant utilities) for rust☆48Updated 10 months ago
- Fast FASTQ sample demultiplexing in Rust.☆62Updated last month
- parallelized blat with multi-threads support☆53Updated 3 months ago
- Kourami: Graph-guided assembly for HLA alleles☆38Updated 5 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆55Updated 7 years ago
- Grep for FASTQ files☆97Updated last month
- A C library for handling bigWig files☆79Updated 4 months ago
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated last week
- Data from the Human PanGenomics Project☆60Updated 3 years ago
- SV caller for nanopore data☆91Updated 4 years ago
- Single-Cell RNA-seq pseudo-aligner☆51Updated last year
- BigWig and BAM utilities☆96Updated last year
- HATCHet (Holistic Allele-specific Tumor Copy-number Heterogeneity) is an algorithm that infers allele and clone-specific CNAs and WGDs jo…☆69Updated 2 months ago
- Assembly Based ReAligner☆73Updated 6 years ago
- CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data.☆38Updated 3 weeks ago
- WDL’s and Dockerfiles for assembly QC process☆66Updated last week