NewPointe / KitchenViewLinks
The order monitoring system for our Cafes.
☆12Updated 4 years ago
Alternatives and similar repositories for KitchenView
Users that are interested in KitchenView are comparing it to the libraries listed below
Sorting:
- Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…☆10Updated 8 years ago
- ☆16Updated 2 years ago
- Utility programs to trim or sort Illumina reads with adapter sequences☆15Updated 12 years ago
- We aim to make it easier for biomedical researchers to access and customize synthetic sequence data for the purpose of sharing and testin…☆11Updated 6 years ago
- Angular.js app for Open Targets Platform☆15Updated 4 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Updated 7 years ago
- A protocol to estimate global ancestry starting from raw Illumina data☆11Updated 6 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Updated 7 years ago
- GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS☆17Updated 6 years ago
- variant integration methods for the 1000 Genomes Project☆21Updated 8 years ago
- ☆15Updated 2 years ago
- Mapping-free variant caller for short-read Illumina data☆20Updated 5 years ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 6 years ago
- Process Illumina instrument data into SAM/BAM/CRAM files.☆10Updated last month
- Tools for doing x way meta-analysis☆12Updated 3 years ago
- Allele frequency filter app☆14Updated 3 years ago
- Toolbox for generic NGS analyses - A framework to quickly build pipelines and to perform large-scale NGS analysis☆18Updated 3 years ago
- Ebola virus surveillance☆15Updated 9 years ago
- program to estimate admixture coefficients from individual genotype or sequence data☆33Updated last year
- As part of the COVID-19 Host Genetics Global initative, this repo serves to corroborate sample scripts for sequencing QC.☆12Updated 5 years ago
- Variant caller GUI + genetic disease analysis☆22Updated 5 years ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Updated 7 years ago
- Code to reproduce analyses from the sleuth paper☆16Updated 7 years ago
- A light-weight HTML lab notebook generator☆18Updated 2 years ago
- Code to do data processing and create figures for "The geography of recent genetic ancestry across Europe", http://arxiv.org/abs/1207.381…☆15Updated 11 years ago
- Targeted and non-targeted anticancer drugs and drug regimens☆30Updated 2 weeks ago
- Simple matching of HTS samples based on HLA typing☆13Updated 9 years ago
- extract SV signal from a BAM☆11Updated 7 years ago
- Program for estimating admixture proportions and doing principal component analysis of a single NGS sample☆11Updated last year
- Tutorial for working with cloud infrastructure and AWS from R☆20Updated 8 years ago