Next Generation Sequencing

Research Services for Cutting-Edge Genomics

Accelerate Your Scientific Discoveries

Mediomix is the premier provider of Next Generation Sequencing (NGS) services tailored to meet the distinct needs of researchers, clinicians, and biotechnologists worldwide. Our highly skilled scientists deliver precise, top-tier genomic data to drive your research endeavors.

Explore Services
NGS Laboratory Research
Whole Genome Sequencing

Complete Genome Analysis Solutions

From Human to Microbial Genomes

Unlock the full potential of genomic information with our comprehensive whole genome sequencing services. We offer scalable solutions for human, animal, plant, and microbial genome analysis with industry-leading accuracy and turnaround times.

Learn More
Genome Sequencing
Metagenomics

Explore Microbial Communities

Environmental & Clinical Microbiome Analysis

Discover the hidden world of microorganisms with our advanced metagenomics services. From 16S amplicon sequencing to shotgun metagenomics, we provide comprehensive solutions for microbiome research and environmental monitoring.

Discover More
Metagenomics Research
AI-Powered Analysis

Advanced Bioinformatics Solutions

From Raw Data to Actionable Insights

Our proprietary AI-powered genomic analysis engine combines machine learning with deep variant annotation for accurate, actionable insights. Get publication-ready results with comprehensive bioinformatics support.

Explore Analysis
Bioinformatics Analysis
DNA Sequencing

WGS, WES, Targeted
Transcriptomics

RNA-Seq & Expression
Metagenomics

Microbiome Analysis
Bioinformatics

Data Analysis
DNA Sequencing

Comprehensive DNA Sequencing Solutions

From whole genome to targeted sequencing, our NGS services provide the depth and accuracy you need for your research. Utilizing state-of-the-art Illumina and PacBio platforms for optimal results.

Whole Genome Sequencing

Comprehensive analysis of entire genomes for complete variant discovery, structural variation detection, and de novo assembly projects.

  • Human, animal, plant & microbial genomes
  • SNP, InDel & structural variant detection
  • Short-read and long-read options
  • De novo assembly capabilities

Whole Exome Sequencing

Focused analysis of protein-coding regions for efficient variant discovery in clinical and research applications with high coverage depth.

  • Comprehensive exome capture
  • Disease variant identification
  • Trio analysis for family studies
  • Clinical-grade interpretation

Targeted Sequencing

Custom panel design for focused analysis of specific genes or genomic regions with ultra-deep coverage for sensitive detection.

  • Custom panel design support
  • Amplicon & hybrid capture methods
  • Low-frequency variant detection
  • Scalable for large cohorts
Our Services

Explore Our NGS Service Portfolio

Comprehensive genomics solutions designed to meet diverse research needs across multiple disciplines and applications.

Whole Genome Sequencing DNA Sequencing

Whole Genome Sequencing

Complete genomic coverage for comprehensive variant discovery, structural analysis, and population studies across all organism types.

Human Animal Plant Microbial
RNA Sequencing Transcriptomics

RNA Sequencing

Comprehensive transcriptome analysis including mRNA, small RNA, and long non-coding RNA profiling with strand-specific protocols.

mRNA-Seq Small RNA lncRNA
Metagenomics Metagenomics

Microbiome Analysis

Explore microbial communities with 16S/ITS amplicon sequencing and shotgun metagenomics for taxonomic and functional profiling.

16S rRNA ITS Shotgun
Single Cell Single Cell

Single-Cell Sequencing

Resolve cellular heterogeneity with single-cell RNA sequencing, ATAC-seq, and multi-modal approaches for comprehensive cell profiling.

scRNA-seq scATAC Multi-omics
Exome Sequencing Exome

Exome Sequencing

Cost-effective analysis of protein-coding regions for clinical diagnostics, rare disease research, and cancer genomics studies.

Clinical Research Oncology
Epigenomics Epigenomics

Epigenetic Analysis

Study DNA methylation patterns, histone modifications, and chromatin accessibility with our comprehensive epigenomics services.

WGBS ChIP-seq ATAC-seq
Transcriptomics

RNA Sequencing & Gene Expression Analysis

Unlock the power of transcriptome analysis to understand gene expression patterns, alternative splicing events, and non-coding RNA regulation. Our RNA-Seq services provide comprehensive insights into cellular function and disease mechanisms with strand-specific, high-depth sequencing.

mRNA Sequencing

Differential expression and pathway analysis

Small RNA Sequencing

miRNA, piRNA, and siRNA profiling

Single-Cell RNA-Seq

Cellular heterogeneity resolution

Alternative Splicing

Isoform discovery and quantification

RNA Sequencing
Metagenomics

Microbiome & Environmental Genomics

Explore microbial communities with our comprehensive metagenomics services. From targeted 16S/ITS amplicon sequencing to whole-metagenome shotgun analysis, we provide complete solutions for understanding microbial diversity, function, and ecology in any environment.

16S/ITS Amplicon

Taxonomic profiling of bacteria and fungi

Shotgun Metagenomics

Functional and taxonomic analysis

AMR Detection

Antimicrobial resistance profiling

Environmental eDNA

Biodiversity monitoring solutions

Metagenomics
Bioinformatics

Advanced Data Analysis Capabilities

Our proprietary AI-powered analysis platform transforms raw sequencing data into actionable biological insights with comprehensive reporting.

Primary Analysis

Base calling, quality filtering, read mapping, and initial data processing with industry-standard pipelines ensuring reproducible results.

Variant Analysis

SNP/InDel calling, structural variant detection, copy number analysis, and comprehensive annotation against multiple databases.

Pathway Analysis

Gene ontology enrichment, pathway mapping, protein-protein interactions, and functional annotation for biological interpretation.

AI/ML Integration

Machine learning models for variant prioritization, biomarker discovery, and phenotype-genotype correlation analysis.

Custom Reporting

Publication-ready figures, interactive visualizations, and customizable reports tailored to your specific research needs.

Secure Delivery

AWS-hosted secure data transfer, long-term storage options, and compliant data handling protocols for all projects.

Applications

Research Applications We Support

Our NGS services power discoveries across diverse research domains, from basic science to clinical applications.

Human Disease Research

Cancer genomics, rare diseases, pharmacogenomics, and complex trait analysis

Agricultural Genomics

Crop improvement, livestock genetics, and agricultural microbiome studies

Environmental Science

Biodiversity assessment, pollution monitoring, and climate research

Infectious Disease

Pathogen genomics, outbreak investigation, and AMR surveillance

Population Genetics

Ancestry analysis, demographic history, and evolutionary studies

Basic Research

Gene function studies, regulatory elements, and epigenetic mechanisms

Dairy Research

Dairy microbiome profiling, fermentation genomics, and quality analysis

Dental Research

Oral microbiome analysis, periodontal disease studies, and dental genomics

Why Mediomix

Why Choose Our Research Services

We are committed to delivering exceptional genomics services that drive scientific breakthroughs and accelerate your research.

01

State-of-the-Art Technology

Access to the latest Illumina and PacBio sequencing platforms for optimal data quality and throughput.

02

Expert Scientific Team

Highly trained scientists with extensive experience in NGS library preparation and data analysis.

03

Comprehensive Analysis

AI-powered bioinformatics pipelines delivering actionable insights and publication-ready results.

04

Dedicated Support

End-to-end project management with dedicated support from consultation to data delivery.

Ready to Accelerate Your Research?

Contact our team of genomics experts to discuss your project requirements. We're here to help you achieve breakthrough discoveries with our comprehensive NGS services.

+91 938 025 1598 support@mediomixdb.com

Request a consultation: www.mediomixdb.com