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RNI TC No. MAHENG14628 RNI NO. DELENG/2004/13061
Date of Publication - 30.11.2022 Date of Posting - 1.12.2022
Research Services
DNA Based #GENOMICSFORALL
• Viral Sequencing Clinical
• Whole Genome Sequencing Genomics
(Bacteria, Fungi, Insects, Human, etc.) • Infectious Diseases
(Tuberculosis, HPV)
RNA Based Epigenetics
• Cancer
• Viral Sequencing • Whole Genome • Whole Exome
• Whole Transcriptome Sequencing Bisulfite Sequencing
• Circular RNA Sequencing Sequencing
• Small RNA Sequencing • MeDIP-Seq • HLA typing
• Long non-coding RNA Sequencing • ChIP-Seq
• RIP-Seq
Metagenomics
Computation
• Shotgun Metagenomics
• Shotgun Metatranscriptomics • Bioinformatics Analysis
• 16S/18S rDNA/rRNA Sequencing • Drug Repurposing
• Fungal ITS Sequencing
WHY • High Sensitivity, Variant calling confidence, Resolution
• High depth and deep coverage
NGS • Multigene testing potential
• High troughput leading to optimum cost
• Range of Genetic Variations possible to detect on a single platform
Multigene High Resolution Upto 4 field Nomenclature HLA Application
HLA
Typing
Exome • Understanding the Coding & UTR regions of your genome through exome analysis.
Analysis • 85% of disease causing variants are found in exomes.
Cancer • Cost effective alternative to WGS.
• Incresed variant discovery potential for population gentics & cancer genetics.
including rare and frequency mutation.
• 35 to 36.5 mb exome reading is possible only through NGS.
• NGS enables precision oncology through precision diagnostics. SOLVING CANCER
• Multiple biomarker testing in cancer for optimal cancer care by maximizing
treatment efficacy and minimizing window period of disease progression. YOU CAN’T CURE WHAT YOU
• Multigene testing on small sample volume. DON’T UNDERSTAND
• High sensitivity testing from liquid biopsy specimens for disease relapse or
monitoring.
www. mibiome.com +91 96502 31515
[email protected] [email protected]
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