No description provided.
## Usage ```typescript import { RNSerialPort } from '@genee/react-native-serialport';
```typescript import { setRemoteBase, setDefaultResources, useI18N } from '@genee/i18n';
```typescript import HCISocket from '@genee/hci-socket';
genee-easyrun ============
```bash pnpm create @genee/uno-app <project-name> ```
这是一个由@genee/labmai开发的组件库
## Installation
## Usage
## Usage
基于 iframe 的父窗口和子窗口的通讯机制实现，支持 React 和 Vue 3。
## Installation ```bash yarn add git+https://github.com/iamfat/json-rpc.git ```
用于维护GPUI组件
## Usage
C-like struct for buffer parsing and packing
## Usage
Light-weight AMD JS loader for specific scene.
Node/Electron module to detect idle desktop users(users away from keyboard) in macOS, Windows, Linux, FreeBSD and OpenBSD
Bluez5 D-Bus library for easy to use bluetooth access in node
## 1. 整合方法
A D-Bus binding for Node
No description provided.
A Camera component for React Native. Also reads barcodes.
No description provided.
A habit tracker app with command-line interface
Spatial gene regulatory network inference and in-silico perturbation (Rust port of SpaceTravLR)
Spatial gene regulatory network inference and in-silico perturbation (Rust port of SpaceTravLR)
A tool to analyze and manipulate transcript segment graph (TSG)
Gene Cluster prediction with Conditional Random Fields
Prismer Cloud SDK — Context API, Parse API, IM, Evolution Engine
Gene-set score per cell (mean of a gene list minus an expression-bin-matched random control set) — matches scanpy tl.score_genes(random_state=0) value-exactly
rvDNA — AI-native genomic analysis. 20-SNP biomarker risk scoring, streaming anomaly detection, 64-dim profile vectors, 23andMe genotyping, CYP2D6/CYP2C19 pharmacogenomics, variant calling, protein prediction, and HNSW vector search in pure Rust.
Pure-Rust port of the GSVA family of gene-set enrichment methods (GSVA, ssGSEA, z-score, PLAGE), validated for numeric parity against the Bioconductor GSVA package.
Count intersections between genes and sequences
Fast and accurate guide counting for CRISPR screens.
Read phylogenetic tree(s) in newick, phyloXML or recPhyloXML file and build a svg representation of the tree(s) allowing 1, 2 or 3 reconciliation levels.
The tool validates the input predicted genes and provides useful information (length validation, gene merge validation, sequence duplication checking, ORF finding) based on the similarities to genes in public databases.
Gene Expression in RBBT
GoRuby makes it easy to interact with the Gene Ontology by using the infrastructure setup in R. By connecting to R using RSRuby, the database and methods can be interrogated. Plus, keeping the R library up to date is much simpler than having to keep a GO implementation up to date.
Parse publications for gene names in a fuzzy fashion
Parses gene ontology .obo files, links terms through `is_a` and provides methods to find levels and traverse the tree.
Data sources like PubMed, Entrez Gene, or Gene Ontology
This bio-gem facilitates the creation of pretty, publication quality SVG images from feature data.
A module which allows the GENE gyrokinetic code to be run using the CodeRunner framework.
CURRENTLY UNDER DEVELOPMENT (not usable yet)
Use this siftware with techniques like genecapture
kittyverse - helper classes for cattributes, trait types, traits, genes, genomes and more for cryptokitties and copycats
FULL-LENGTHERNEXT is a tool adapted to NGS technologies, able to work in parallel and in a distributed way to minimise computing time. It is able to classify unigenes to full-length, 5’-end, 3’-end and internal, suggesting which unknown genes are coding or not. It will be also shown that FULL-LENGTHERNEXT fixes frame shifts, one of the main mistake found in wrong entries of full-length sequences databases, and it is a fast tool to compare different transcriptome assemblies.