Whole Genome Sequencing Revolutionary and Necessary
Leverage the power of tech-driven Whole Genome Sequencing with Yaazh Xenomics!
Experience The Power Of Scalable, Flexible NGS Technology
Get the power of the complete DNA sequence of any organism with our Whole Genome Sequencing services. It is also known as entire genome or full genome sequencing and is one of the best tools in your arsenal to detect rare variants.
With our comprehensive data set on any genome, you can evaluate all structural variation in the strain or organism. Make our WGS services the instrument for identifying mutations or inherited disorders. Use it to track disease outbreaks. We offer whole genome or complete genome sequencing not just for human genomes but also plants, microbes and livestock too!
Cutting-Edge Platforms
HiSeq2500 (250)
GS FLX Titanium Plus (Shotgun, Mate pair)
HiSeq X Ten
MiSeq (Mate pair, Paired end)
A Powerful Tool For You
Whole genome sequencing is the tool you need to draw concrete DNA sequences. Get in touch to learn more about our methods.
Our Whole Genome Sequencing, Your Asset
Excellent Clarity
We offer a base-by-base genome view in high resolution so that you get a clear picture of the structural variations.
Perfect Capture
We offer clear target capture of small and large variants. Even the captures which could have been missed with targeted approaches are also perfectly captured.
Identify Causes
We assist follow-up studies related to the regulation mechanism and gene expression by identifying potential causative variants clearly.
Deliver Data
We offer high-quality, high-volume data within just a short time span and offer support to the assembly of novel genomes.
Two Strands of WGS
At Yaazh, we offer two types of whole genome sequencing - De Novo sequencing and Re-sequencing.
Whole Genome De novo sequencing
De novo sequencing is usually performed without the help of a reference genome. It is also considered to be effective in confirming and re-reading on the results generated from existing ones. This is helpful to create comprehensive maps to genomes by utilizing multiple the various combinations of sequencing platforms such as HiSeq, MiSeq, NovaSeq.
Whole genome Re-sequencing WGS
WGS re-sequencing uses the reference sequence of a particular genome is available. The sample that can be sequenced will be successful at lower level, and the event suggested as a reference. In this, we can create an organisms individual variation from the genome mapping it. The variation can be SNP( Single nucleotide polymorphism), CNV (copy number variations), somatic mutations and Indels(insertion/deletions).