Next-Generation Sequencing
State-of-the-art NGS on Illumina NovaSeq, NextSeq, Oxford Nanopore and MGI platforms — WGS, WES, RNA-Seq, metagenomics and more, with expert bioinformatics and competitive pricing.
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Talk to our NGS specialists about platform choice, data output and bioinformatics for your study.
Explore Next-Generation Sequencing
Sequencing and analysis services across our NGS platforms.
Whole Genome Sequencing
Complete end-to-end sequencing of an organism's entire genome for variant discovery and de novo assembly.
Transcriptome Sequencing
RNA-Seq profiling of the full set of transcripts to measure gene expression and identify novel transcripts.
Epigenome Sequencing
Genome-wide profiling of DNA methylation and epigenetic modifications that regulate gene activity.
Direct RNA Sequencing
Native RNA sequencing on Nanopore to read full-length transcripts and detect base modifications without reverse transcription.
Hybrid Sequencing
Combined short- and long-read sequencing for highly accurate, contiguous genome assemblies.
Hybrid Transcriptome Sequencing
Short- and long-read RNA-Seq combined to capture full-length isoforms with quantitative accuracy.
Metagenome Sequencing
Shotgun sequencing of entire microbial communities to characterise species composition and function.
Nanopore Sequencing
Real-time long-read sequencing on Oxford Nanopore for structural variants and full-length reads.
Bioinformatics Services in India
Downstream analysis, assembly, variant calling and interpretation delivering publication-ready results.
NGS Price Packages in India
Transparent, competitive pricing packages for sequencing and bioinformatics projects of any scale.