Next-Generation Sequencing (NGS)

Deciphering complexity through high-throughput genomic insight
At Decipher Genomics & Research, our advanced NGS services empower researchers, clinicians, and innovators with scalable, high-resolution data across molecular layers. From individual genomes to complex microbiomes, our platforms are optimized for discovery and translational science.
Our cutting-edge sequencing centre in Ahmedabad, Gujarat, India, harnesses the world’s most advanced platforms to deliver reliable, high-resolution NGS data across domains. With quality as our cornerstone, we utilize leading technologies from:
- Illumina (NovaSeq 6000, NovaSeq X Plus, MiSeq)
- Thermo Fisher Scientific (Ion Torrent S5 Plus)
- PacBio (Revio /Vega)
- Nanopore Technologies
As a trusted partner in India’s genomics ecosystem, we ensure every dataset is generated under globally aligned standards for integrity, traceability, and reproducibility.
Next-Generation Sequencing Platforms
We utilize a diverse suite of state-of-the-art sequencing technologies to deliver fast, accurate, and scalable results for a wide range of applications.

NovaSeq 6000 system

NovaSeq X Plus

PacBio Revio

Ion GeneStudio S5 Plus & Ion Chef

Nanopore Technologies
What Sets Decipher Apart
- Optimized, validated protocols for diverse sequencing workflows
- Experienced team of scientists, clinicians, and bioinformaticians across human, animal, microbial, plant, insect, and environmental genomics
- End-to-end support, from experimental design and library preparation to bioinformatics, annotation, and custom reporting
- ISO-compliant systems and stringent QC checkpoints to ensure scientific confidence
At Decipher, technology meets expertise to decode life’s complexity with precision and purpose.
Our NGS Portfolio
- Genome Sequencing Comprehensive analysis of entire genomes for variant discovery, comparative genomics, and evolutionary research.
- Whole Transcriptome Sequencing (Total RNA-Seq/mRNA Seq) In-depth expression profiling of coding and non-coding RNAs, uncovering splicing patterns, gene fusions, and pathway regulation.
- Small RNA Sequencing Accurate quantification of miRNAs, siRNAs, and piRNAs to explore gene silencing and post-transcriptional control mechanisms.
- Genotyping by Sequencing (GBS) Targeted, cost-effective SNP detection across populations—ideal for breeding, QTL mapping, and association studies.
- Metatranscriptomics & Metagenomics Shotgun sequencing of environmental and host-associated samples for microbial diversity, function, and community gene expression.
NGS Methodology
Precision protocols for superior data integrity
At Decipher Genomics & Research, we follow a rigorous, quality-driven approach to ensure robust and reproducible sequencing outcomes:
- Sample Compatibility: We accepts High-quality Nucleic acids or Samples as per sequencing needs
- Quality Control: Stringent QC at every stage—from input DNA integrity to post-library validation
- Library Preparation: Utilizes optimized protocols and kits to prepare NGS libraries adapted to genome size and complexity
- Sequencing Platforms: Utilizes advanced sequencing technologies as per the project requirements to achieve comprehensive coverage and resolution.
Deliverables
Comprehensive data, ready for action
- Raw sequencing data in FASTQ format
- Bioinformatics report including alignment statistics, genomic coverage, and structural variant identification
- User-ready outputs delivered in annotated, accessible formats for direct downstream use
Why Choose Us
- Integrated sample-to-annotation workflow
- Platform flexibility for DNA, total RNA, small RNA, and metagenomic inputs
- Secure, ISO-compliant data management
- Expert bioinformatics support and custom reporting
Decoding Complexity. Delivering Insight. Driving Discovery.