Solutions
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SMART BIOINFORMATICS
Our vision is to make solutions for genomic tests helping clinicians and diagnostic labs with far-reaching impacts on the current as well as foreseen healthcare challenges. With our high efficacy and shorter turn-around time, we plan to accelerate the biomedical industry.
We Understand Your Needs
Customized Solutions
Our solutions are tailored to meet your specific needs and requirements of its clients, ensuring maximum accuracy and efficiency in genomic analyses.
Personalized reports
Our personalized clinical reports offer insights into genetic variants, disease risk, and personalized treatment options.
- Identification of evidence-based actionable markers (Single Nucleotide Variants (SNVs), Insertions and Deletions (Indels), Copy number variations (CNVs) and gene-fusions)
- Machine learning based scoring of variants based on guidelines provided by Association of Molecular Pathology (AMP) and ACMG
- Detailed interpretation about the variants and the associated genes
- Information about interventions or therapies associated with the variants
ONQUER
(Targeted Oncopanel Solution)
- Identification of evidence-based actionable markers (Single Nucleotide Variants (SNVs), Insertions and Deletions (Indels), Copy number variations (CNVs) and gene-fusions)
- Machine learning based scoring of variants based on guidelines provided by Association of Molecular Pathology (AMP) and ACMG
- Detailed interpretation about the variants and the associated genes
- Information about interventions or therapies associated with the variants
Anuvanshiki
A specialized genome-informatics solutions designed to analyze germline samples, which are inherited from parents. By focusing on the genetic material passed down from generation to generation, Anuvanshiki aims to pinpoint specific mutations associated with hereditary disorders.- Evidence-based genomic variants (Single Nucleotide Variants (SNVs), Insertions and Deletions (Indels), Copy number variations (CNVs)
- Machine learning-based scoring of variants based on guidelines provided by the American Council of Medical Genetics (ACMG)
- Detailed interpretation of the variants and the associated genes
- Information about interventions or therapies associated with the variants
A specialized genome-informatics solutions designed to analyze germline samples, which are inherited from parents. By focusing on the genetic material passed down from generation to generation, Anuvanshiki aims to pinpoint specific mutations associated with hereditary disorders.
Our results will empower medical decisions
Immense Expertise
Genome informatics is our Forte
Fast Turnaround Time
Accelerate your Analysis
Advanced Analysis
Cutting edge high quality analysis
User Specific Downstream Analysis
Customized Analysis
High Level of Support
Re-Analysis of Samples