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Whole Genome Sequencing (WGS) Services | Comprehensive DNA Analysis in India

Perfectly tailored genomic services that enhance our resources to detect rare variants and structural variants.

Genome Sequencing: A Comprehensive Tool

Yaazh Xenomics uses a diverse spectrum of ingenious technologies and scientific solutions to accurately determine a particular organism's genome's complete DNA sequence. Whole Genome Sequencing (WGS) is done with exceptionally high levels of quality and compliance. We have unmatched expertise,evidence-based knowledge, and an excellent Whole Genome Sequencing lab to facilitate the detailed evaluation of the genetic variations of a single strain.

Yaazh Xenomics delivers industry-leading Whole Genome Sequencing (WGS) services using state-of-the-art short-read and long-read technologies. From our advanced laboratory in Coimbatore (with services extended to Visakhapatnam), we provide complete, high-resolution sequencing of entire genomes — enabling discovery of SNPs, Indels, copy number variations (CNVs), structural variants (SVs), and rare genetic variants with exceptional accuracy and depth.

Genome Sequencing: A Comprehensive Tool

Whole Genome Sequencing Test We Offer using various platform

Illumina Novaseq Platform

Nanopore Platform

Thermo S5 Plus

MGI Platform

What is Whole Genome Sequencing (WGS)?

<p>Whole Genome Sequencing determines the exact order of nucleotides (A, T, C, G) across the entire genome of an organism — including coding regions, regulatory elements, introns, and non-coding DNA. Unlike targeted panels or exome sequencing, WGS provides an unbiased, base-by-base view, making it the gold standard for comprehensive genomic analysis.</p><p>Modern WGS combines high-throughput Next-Generation Sequencing (NGS) platforms with advanced bioinformatics pipelines to detect even the most complex genetic variations that other methods might miss.</p>

Advanced Platforms & Technologies

  • <strong>Illumina NovaSeq Series</strong> — Ultra-high throughput, exceptional accuracy for deep coverage resequencing
  • <strong>Oxford Nanopore Technology</strong> — Long-read sequencing (up to hundreds of kb) for resolving complex regions, repeats, and structural variants
  • <strong>MGI Sequencing Platform</strong> — Cost-effective, high-quality short-read sequencing
  • <strong>Thermo Fisher Ion S5 Plus</strong> — Flexible semiconductor-based sequencing for targeted or smaller genome projects

Ready for Your Whole Genome Sequencing Project?

Contact our genomics experts today for a free consultation, customized experimental design, coverage recommendations, and a competitive quote.