An online platform for streamlined Next-Generation Sequencing analysis. Perform alignment, SNV, MSIndel and CNV calling, and HLA typing without the need for complex commands.
We are a dedicated team, aim to simplifying genomic data analysis by providing an intuitive platform for performing common NGS pipelines. Our mission is to make advanced genomic analysis accessible to researchers and clinicians without the need for complex command-line tools.
Accurate alignment of sequencing reads to reference genomes using cutting-edge algorithms.
Identify single nucleotide variants with high precision and sensitivity.
Detect microsatellite instability and indels for comprehensive genomic profiling.
Analyze copy number variations to uncover genomic alterations.
Perform accurate HLA typing for immunogenetics research and clinical applications.
Upload your data securely via our web interface or encrypted transfer protocols.
Access and manage your files and results through a private, user-friendly dashboard.
Integrate our platform into your workflows using our secure API endpoints.
Create your free account to get started with our platform.
Upload your .bam or .fastq files via our secure web interface.
Choose the analysis pipeline that suits your research needs.
Your data is processed using high-performance computing resources.
Download your results from your dashboard or via API.
Interpret your data with confidence and advance your research.
Basic pipelines with limited file size.
Pay only for what you use.
Access all pipelines with a monthly fee.