India’s genomics ecosystem is entering a phase of accelerated growth driven by precision medicine, rare disease research, and large-scale population genomics initiatives. Yet, despite this momentum, many genomics workflows remain fragmented, spread across multiple technologies, platforms, and processes, often leading to variability, inefficiencies, and delayed inferences with data analysis.
At Spinco, we enable integrated, end-to-end genomics workflows bringing together best-in-class technologies across the entire continuum, from nucleic acid extraction, reagents and oligonucleotide solutions, and precise sample preparation to advanced sequencing, spatial genomics and high-resolution data generation. As a trusted solution partner in India, we go beyond individual platforms to design workflows that are cohesive, scalable, and aligned to real-world translational research needs.
An integrated suite of advanced genomics technologies spanning the full workflow from sample preparation to data analysis, delivering scalable, high-fidelity, and application-agnostic solutions to address diverse and complex biological research needs.
PacBio HiFi sequencing sets the gold standard in modern genomics by uniquely combining long read lengths with exceptional accuracy, eliminating the traditional trade-off between read length and precision. The result is a complete view of the genome for confident detection of complex variants & repeat regions.
n6Tec iconPCR enables intelligent real-time amplification through AutoNorm, delivering normalized sequencing-ready libraries in a single automated step while eliminating the need for individual cleanup and extra reagents and ensuring consistent performance with high-quality data from every sample.
Yourgene Health leverages Ranger Technology to deliver dynamic DNA size selection with integrated fragment analysis and fluorescence-based quality control, enabling automated, high-precision workflows that support diverse applications from oncology and gene synthesis to NIPT and beyond.
Vizgen’s MERFISH technology enables highly multiplexed spatial transcriptomics by imaging thousands of RNA molecules within intact cells, delivering precise, single-cell resolution maps of gene expression while preserving spatial context to power deeper biological insights and discovery.
Revvity advances genomic automation with seamlessly integrated solutions that combine precision, scalability, and performance, streamlining workflows from sample to analysis while ensuring accuracy and reproducibility across the entire genomic continuum.
IDT empowers end-to-end genome engineering with a comprehensive CRISPR workflow and precision gene synthesis solutions, combining optimized Cas systems, customizable gRNAs, HDR tools, and high-quality gene fragments to accelerate innovation from design to analysis in synthetic and molecular biology.
Hamilton Storage delivers integrated sample management systems that seamlessly connect with Hamilton Robotics liquid handling workstations and a wide range of automated devices, creating a flexible, end-to-end sample processing solution tailored to diverse laboratory needs.
OligoMaker APS delivers flexible, high-throughput DNA and RNA synthesis, enabling the simultaneous production of up to 1536 primers and probes in a single run while ensuring seamless workflows and scalable performance for advanced research.
A streamlined, comprehensive genomics workflow integrating automation, precision, and scalability from sample handling to high-quality sequencing output.
Reliable genomics workflows begin with secure sample storage, traceability, and efficient sample accessibility across high-throughput environments. Automated storage and retrieval systems help maintain sample integrity, minimize manual intervention, and improve overall workflow efficiency.
High-quality DNA and RNA extraction is essential for ensuring reproducible sequencing performance and accurate downstream molecular analysis. Automated extraction workflows deliver consistent nucleic acid recovery, scalability, and reduced operator-dependent variability across diverse sample types.
Accurate quantification and quality assessment are critical for optimizing library preparation efficiency and sequencing outcomes. Integrated QC workflows enable precise evaluation of nucleic acid concentration, integrity, and fragment distribution prior to downstream processing.
Library preparation directly impacts sequencing sensitivity, reproducibility, and overall data quality in genomics workflows. Automated and standardized preparation workflows help reduce bias, streamline normalization, and support scalable high-throughput sequencing applications.
Precise size selection and cleanup are essential for generating high-quality sequencing libraries with improved uniformity and performance. These workflows are particularly important for low-input, cfDNA, and advanced NGS applications where library consistency influences downstream analytical accuracy.
High-accuracy long-read sequencing enables comprehensive characterization of structural variants, repeat regions, transcript isoforms, and complex genomic landscapes. These capabilities support advanced genomic applications across translational research, oncology, rare disease, and population-scale genomics initiatives.
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