CBSR-Biobank / biobankLinks
Biorepository application for tracking biospecimens.
☆22Updated last year
Alternatives and similar repositories for biobank
Users that are interested in biobank are comparing it to the libraries listed below
Sorting:
- Moved to: https://github.com/maxplanck-ie/parkour2☆33Updated 3 years ago
- Snakemake skeleton - Build workflows with Snakemake☆19Updated last year
- Web based LIMS☆102Updated this week
- Seven Bridges API Client, CWL Schema, Meta Schema, and SDK Helper in R☆35Updated 3 years ago
- GeneSCF moved to a dedicated GitHub page, https://github.com/genescf/GeneSCF☆20Updated 4 years ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 5 years ago
- Repository for documentation to support the IEEE 2791-2020 standard. Please see our home page for communications/publications:☆17Updated last year
- Toolbox for generic NGS analyses - A framework to quickly build pipelines and to perform large-scale NGS analysis☆18Updated 2 years ago
- Candidate Drivers Analysis: Multi-Omic Search for Candidate Drivers of Functional Signatures☆24Updated 11 months ago
- Script to calculate polygenic risk scores in a genotyped sample using GWAS summary statistics from a disease/trait.☆18Updated 7 years ago
- Generate HTML report for a set of genomic regions or DESeq2/edgeR results☆10Updated 7 months ago
- Predicting oncogenic potential of gene fusions☆12Updated 9 years ago
- Integrative visualization of multiple omic datasets onto KEGG pathways.☆11Updated 3 years ago
- A web-based application to perform Over-Representation Analysis (ORA) using clusterProfiler and shiny R libraries☆12Updated 5 years ago
- MOLGENIS - for scientific data: management, exploration, integration and analysis.☆118Updated last month
- A tool to detect postzygotic single-nucleotide mosaicism from unpaired, trio, or paired samples.☆13Updated 4 years ago
- NExt generation Analysis Toolbox☆14Updated 9 years ago
- A webtool for the clinical interpretation of CNVs in rare disease patients☆12Updated 3 years ago
- A server for maintaining high-throughput sequencing QC data☆13Updated 3 weeks ago
- ☆16Updated 7 years ago
- Clinical Variant Annotation Pipeline☆10Updated 5 years ago
- RNA-seq for Mendelian disease diagnostics: A hands-on tutorial through bioinformatic tools and workflows☆17Updated 3 years ago
- GUI for batch primer design with graphical output for PCR and SNP detection☆17Updated 7 years ago
- A fast, easy way to present complex bioinformatics pipelines to biologists☆11Updated 6 years ago
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆33Updated 3 years ago
- Allele frequency filtering for Mendelian variant discovery☆18Updated 8 years ago
- A set of command line tools based on R and JavaScript.☆18Updated 5 years ago
- Framework to benchmark algorithms when detecting germline copy number variations (CNVs) from NGS data☆14Updated 8 months ago
- Proof of concept to use ansible + Lmod to deploy a bioinformatics server☆24Updated 2 months ago
- H3ABioNet 16S rDNA diverstity analysis package☆19Updated 6 years ago