StrandOmics Description
Efficiently generating reports for NGS-based clinical tests necessitates a well-established and sophisticated platform that can automatically prioritize variants, interpret clinical data, and create comprehensive reports. Strand Omics serves as a rapid, HIPAA-compliant cloud platform that enhances our clinical diagnostics efforts, having been refined over four years through the analysis of more than 10,000 clinical reports and numerous peer-reviewed studies. This platform integrates advanced bioinformatics algorithms with curated databases, intuitive visualization tools, and robust reporting features. It is designed with specialized workflows tailored for both rare inherited conditions and somatic tumor profiling assays. Additionally, the system boasts a library of over 10,000 somatic variants that have been curated for their oncogenic potential, alongside 100 genes selected for their druggability across various cancer types, as well as 500 drugs that have been validated for efficacy against multiple cancers. Furthermore, its comprehensive approach ensures that healthcare professionals have access to critical data, ultimately facilitating informed decision-making in patient care.
StrandOmics Alternatives
Built for testing laboratories, QBench is a cloud LIMS that brings samples, workflows, lab data, inventory, reporting, quality processes, and client interactions into a single system.
From order placement through sample processing, results, and automated reporting, QBench supports every stage of lab operations. Lab teams configure their own workflows, data fields, and automation rules, so the software fits existing processes instead of forcing new ones. When requirements shift, labs can adjust fields, processes, and automations without depending heavily on custom code.
Instruments, software, and outside systems connect to QBench through file parsers and a robust API, which moves data automatically and limits repetitive entry and transcription mistakes. For reporting beyond the LIMS, labs can connect QBench to Tableau, Power BI, Domo, or Looker via REST API.
What labs get with QBench:
Sample and workflow management
Configurable workflows and custom data fields
Workflow automation
Instrument and system integrations
File parsing and API connectivity
Inventory management
A client portal
Automated reporting
Analytics and operational insights
Connections to Tableau, Power BI, Domo, and Looker
A built-in Quality Management System (QMS)
Because it runs in the cloud, lab teams get secure access to their data, workflows, quality management, and reporting in one centralized platform. Implementation and ongoing guidance come from a team that includes former bench scientists who understand laboratory workflows.
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SciSure is a Scientific Management Platform built to support the full range of laboratory operations for scientific organizations. It combines ELN, LIMS, and Health & Safety functionality, giving teams a single system to document experiments, track sample lineage, manage chemical inventory, and run structured, audit-ready compliance processes.
Instead of relying on disconnected systems, organizations get one governed platform that improves reproducibility, increases visibility into lab operations, and reduces risk as they scale.
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VSClinical
VSClinical facilitates the clinical analysis of genetic variants in accordance with ACMG and AMP guidelines. Its structured workflow supports adherence to the American College of Medical Genetics (ACMG) standards, which are essential for identifying and categorizing pathogenic variants related to inherited disease risk, cancer susceptibility, and rare disease diagnosis. The combined ACMG/AMP guidelines for variant interpretation establish a framework for scoring variants and categorizing them into one of five classification levels. Implementing these guidelines necessitates a thorough examination of annotations, genomic contexts, and pre-existing clinical insights for each variant. VSClinical streamlines this process by offering a customized workflow that evaluates each relevant criterion and supplies comprehensive bioinformatics, literature references, and clinical knowledgebase evidence to aid in the scoring and interpretation of variants. This innovative approach is designed to enhance the efficiency of variant scientists as they navigate the complexities of variant processing and analysis. Overall, VSClinical stands out as a vital tool for accelerating the understanding and classification of genetic variants in clinical settings.
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BigOmics Analytics
BigOmics Analytics is an innovative startup focused on biodata analytics, creating platforms that empower biologists to effectively visualize and interpret their omics data. Our primary offering, Omics Playground, is a highly intuitive bioinformatics tool tailored for RNA-seq and proteomics, enabling users to store their experimental data and visualize it interactively. With more than 18 interactive analysis modules and over 150 dynamic plots, the platform supports co-analysis with a vast array of more than 6,000 public datasets, in addition to providing access to more than 50,000 public gene sets and pathways. Furthermore, it seamlessly incorporates drug connectivity and drug sensitivity databases, featuring an extensive collection of over 30,000 drug expression profiles. BigOmics Analytics is designed to promote collaboration between biologists and bioinformaticians, allowing users to uncover insights while minimizing the time spent on data analysis, all without the need for any programming knowledge. The platform's commitment to producing reliable and reproducible results is achieved through the implementation of state-of-the-art methodologies. Ultimately, BigOmics Analytics is revolutionizing the way biological data is analyzed and understood.
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Integrations
No Integrations at this time
Company Details
Company:
Strand Life Sciences
Year Founded:
2000
Headquarters:
India
Website:
strandls.com/bioinformatics/
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Product Details
Platforms
Web-Based
Types of Training
Training Videos
Customer Support
Business Hours
Online Support
StrandOmics Features and Options
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