Whole Genome Sequencing
Whole Genome Sequencing (WGS) is a genomics technique that systematically sequences the genomic DNA of an organism. Its principle is to randomly fragment genomic DNA and construct a sequencing library, then read huge numbers of short sequences through high-throughput sequencing platforms massively and in parallel, followed by bioinformatic alignment and assembly to reconstruct the complete genome. We could identify the genetic variants such as mutation sites, SNPs, insertions/deletions (InDels), and structural variations by WGS, making it a foundation for genetic disease research and gene function analysis.
| PID | Service Description | Academic Price | Turnaround (weeks) | Materials | Deliverables |
|---|---|---|---|---|---|
| D004 | Whole Genome Re-sequencing (for variant discovery)* | 300 USD for one sample (including the worm sample preparation) | 8 | 1. Background strain 2. Target strain | 1. Quality report(.pdf) 2. FASTQ raw data files |
*: If you want to try the de novo sequencing (for novel genomes), please contact us and we will estimate the price for you.
How to Order:
Download the order form OR Start your inquiry
Have Other Questions?
You can always reach us at service@sunybiotech.com. Our customer service and editing experts will get back to you ASAP.
