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SMART-OneTM (Sequence and Meta-Analysis Research Toolkit) is a powerful tool for analyzing genomic data in a clinical setting. With its automated pipeline for analyzing next-generation sequencing data, SMART-OneTM can help clinicians and researchers identify genetic variants associated with rare or undiagnosed genetic disorders, and interpret their clinical significance. By providing a comprehensive view of a patient's genetic makeup, SMART-OneTM can helps in better clinical outcomes.
AGRITTM (Agri-Genomics Research Innovation Toolkit) is a valuable tool for researchers and agricultural professionals working to improve crop and livestock genetics. By analyzing genomic data from plants and animals, AGRITTM can help identify desirable traits, such as disease resistance or high yield, and inform breeding strategies. AGRITTM can also help researchers understand the genetic basis of these traits and develop new methods for improving agricultural productivity.
SMART-OneTM (Sequence and Meta-Analysis Research Toolkit) is a versatile tool for researchers working in basic and applied genomics research. By analyzing genomic data from a wide variety of sources, including whole genome sequencing, whole exome sequencing, mitochondrial genome sequencing, and RNA sequencing, SMART-OneTM can help researchers study the genetic basis of complex diseases, understand the evolution of different species, and develop new genomic technologies. With its automated pipeline and comprehensive analysis capabilities, SMART-OneTM can help researchers accelerate their genomic research and development projects.
As genomics field becomes more mainstream in the life science arena, sequencing of Human, Plant, Animal, and Microbial etc. of DNA base pairs is critical to identifying CNVs/SNPs, mutations etc. that can cause disease. Advancements in high-throughput Instruments has decreased the cost of sequencing but also increased the huge amount of data that requires analysis in shorter time.
The exponential growth of genomics data poses a great challenge for data management and analysis.
Accelerating Genomic Data Analysis with ComputeGenomics
Leveraging CPU/GPU-based approaches to accelerate this data analysis can vastly decrease runtime and costs compared to traditional or normal system.
ComputeGenomics is a specialized platform designed for high throughput genomics data analysis. Dedicated pipeline for genomic studies like variant calling, Genotyping, Expression studies, GWAS, eQTLs, Plant and Animal breeding genetics.
Specialized pipelines for cancer genomics, whole genome to exome sequencing, and whole transcriptome to single cell analysis.
We provide a system tailored for you.
Enterprise-quality hardware is optimized around your organization’s goals and can scale to grow with you.
Our scale-out network-attached storage (NAS) systems start with standard configurations of 12, 48, and 110 TB of usable storage.
Our custom solutions go beyond 110 TB and can scale to 450 TB.
We help integrate our Solutions seamlessly into your lab or data centre.
Verify proper connectivity with your instruments,
Your data remains on site and private, available to share only with users you specify.
Every solution includes one year of on-site hardware and software support.
Additionally, your solution includes one year of direct access to storage administrators for support with integration, network connection, and data management.
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