Whole exome sequencing is a powerful tool to investigate genetic variations underlying cancers, Mendelian diseases, and complex human disorders.
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Whole Exome sequencing services: Ion Torrent Certified Service Providers The Ion Torrent Certified Service Provider program is a global network of validated service providers that enable researchers in small- and medium-sized laboratories to get high-quality exome ...
Learn about what whole exome sequencing is, why it’s important, and how it’s furthering discoveries in cancer research.
Brief Strengths Process Requirements Brief Whole-exome sequencing (WES) is the most frequently used genome sequencing method. Exons are protein coding regions of human genome, and their DNA can be captured and enriched by sequence capture t
Sequencing & analysis IDT ALIGN℠Program Method data Library preparation and hybridization capture To assess the xGen Exome Hyb Panel v2, twelve libraries were prepared using 100 ng of human genomic DNA (Coriell Institute). Then, xGen Stubby Adapters and Unique Dual Indexing primers (UDIs) were...
Whole exome sequencing Most of the DNA sequence variants that lead to alterations in protein function are located in exons, which encompass approximately 1% of the genome. By specifically targeting exon regions, whole exome sequencing is a simple and efficient approach to identify rar...
Our whole genome sequencing services use cutting-edge technologies and bioinformatics to deliver high-quality data and analysis for your genome of interest. Whether you are studying human, animal, plant, bacteria, or virus species, we have a range of WGS services to cater to your unique research...
Supporting Services Data Sciences Back Bioinformatics Biostatistics Software claraT Report Back Publications, Posters & Presentations Fact Sheet Brochure Complimentary Webinar How to use claraT RNA Blog Whole Exome Sequencing (WES) Service Whole Genome Sequencing...
Using Next Generation Sequencing methodology, we provide sequence information that spans the complete genome, which is comprised of approximately 3.2 billion base pairs. In contrast to Whole Exome Sequencing, WGS provides sequence information spanning coding, non-coding, and intergenic regions as well ...