96 Open source projects that are alternatives of or similar to civic-client

🚀 Handy dynamic styles utilities for React Native and React Native Web.

MAGERI - Assemble, align and call variants for targeted genome re-sequencing with unique molecular identifiers

Single-cell copy number calling and event history reconstruction.

Recursive Variant: A simple library for Recursive Variant Types

Aplicativo para o projeto "Anjos do SuperAção"

Rare variant test software for next generation sequencing data

A scalable styled-component theming system that fully leverages JavaScript as a language for styles authoring and theming at both local and global levels.

A neoantigen calling pipeline begins from variants record file (MAF) (Not maintain now)

xHLA: Fast and accurate HLA typing from short read sequence data

Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products

Classifies genes as an oncogene, tumor suppressor gene, or as a non-driver gene by using Random Forests

Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.

Federated Learning based Deep Learning. Docs: https://fets-ai.github.io/Front-End/

Cross-platform normalization enables machine learning model training on microarray and RNA-seq data simultaneously

Unleash is the open source feature toggle service.

Summarize, Analyze and Visualize MAF files from TCGA or in house studies.

DELLY2: Structural variant discovery by integrated paired-end and split-read analysis

A community-maintained repository of cancer clinical knowledge bases and databases focused on cancer variants.

Chromosome visualization for the web

Personal Cancer Genome Reporter (PCGR)

Lollipop-style mutation diagrams for annotating genetic variations.

Microassembly based somatic variant caller for NGS data

fast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"

Training and evaluating a variational autoencoder for pan-cancer gene expression data

An ensemble approach to accurately detect somatic mutations using SomaticSeq

microsatellite instability detection using tumor only or paired tumor-normal data

identifying mutational significance in cancer genomes

Python package to annotate and visualize gene fusions.

Snakemake-based workflow for detecting structural variants in WGS data

Unix, R and python tools for genomics and data science

cBioPortal for Cancer Genomics

Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs

Amaze UI, a mobile-first and modular front-end framework.

The adaptive interface system for modern web experiences.

JavaScript library to display interactive medical images including but not limited to DICOM

The OHIF Medical Imaging Viewer is for viewing medical images. It can retrieve and load images from most sources and formats; render sets in 2D, 3D, and reconstructed representations; allows for the manipulation, annotation, and serialization of observations; supports internationalization, OpenID Connect, offline use, hotkeys, and many more features.