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Invent & Develop:

The Future of Computing Technologies for Bioinformatics

See our ProductsSee Products 

BALSA/ELSA

Economic, fast and accurate genome analysis software solution. 

BALSA/ELSA allows organisations to analyse data quickly without additional investments in large computing systems. 

Fast

Takes only 4.08 hours to process a 50-fold whole genome sequence (WGS) sample, or 10 minutes for a 200-fold whole exome sequence (WES) sample. 

Accurate

Validation with the NIST Genome In A Bottle standard demonstrates that BALSA/ELSA has the highest combined sensitivity and specificity.

Compatible

Outputs variants in VCF, alignment results in SAM/BAM format and stores a SNAPSHOT for efficient storage and indexing.

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Helicube

Hardware-software solution for next generation sequencing (NGS) data analysis

Scalable

Helicube schedules and spreads out jobs to the worker units in the cluster. It then executes the jobs in parallel to achieve horizontal scalability.

Extensible

Helicube can adapt new analysis tools and configure them to run on its platform.

System Management

Monitor system health, loading speed and utilisation using Helicube's administration panel. 

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BGI Online

Analyse, store and share
your genomics data securely.

BGI Online helps you to do genome sequencing and analysis projects, while eliminating software setup and file transfer logistics.

It is a secure cloud platform for bioinformaticians to advance life-saving research.

Big Data

Access the world’s largest repository of genetic data.

Design Analysis

Create your own pipelines or use our best practices. 

Share Findings

Share your findings to clients and peers. 

Visualise Results

Visualise your results using database.bio.

Go to bgionline.com

database.bio

Genome analysis visualised.

database.bio delivers genomic insights into genetics research and everyday medical practice through flexible, robust and secure web application.

Heuristic

database.bio uses a configurable decision tree to help rapidly prioritise genetic variants into five pathogenicities.

Variant

Each genetic variant is presented with human-readable annotations with links to external supporting evidence.

Technology

Includes over 30 databases and 120 annotation types for analysing panel, exome, or genome variants.

Learn More
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