Whole-Exome sequencingGenomic medicinePersonal genome sequencingPersonalize medicineNext-Generation Sequencing technology provides remarkable opportunities to characterize personal or individual genome sequencing and to identifying mutations relevant for disease diagnosis and therapy. The Whole-Exome sequencing using...
Leveraging the ultrahigh-multiplex PCR approach of Ion AmpliSeq technology and the superior accuracy of the new Ion GeneStudio S5 Systems, the Ion AmpliSeq Exome RDY Kit allows for rapid, accurate sequencing of key exonic regions of the genome, going from DNA ...
About Whole Exome Sequencing The exome, comprising about 30 million base pairs and representing 22,000 genes, makes up roughly 2% of the genome. It is estimated that approximately 85% of disease-causing variants can be found within these protein-coding regions. WES therefore allows for a ...
Exome sequencing is a fast and affordable alternative to using whole genome sequencing for your research, allowing you to identify somatic and germline genetic variants within coding regions of genes without the additional expense and data analysis challenges associated with whole genome s...
exome sequencing is a strategy to selectively sequence the coding regions of the genome to identify novel genes associated with rare and common disorders. From: Emery and Rimoin's Principles and Practice of Medical Genetics (Sixth Edition), 2013 ...
Learn about what whole exome sequencing is, why it’s important, and how it’s furthering discoveries in cancer research.
Benefits of whole exome sequencing Using NGS technology gives researchers more comprehensive data and more discovery power than can be achieved through PCR. Since WES is targeted sequencing, it results in a more manageable data output (~5 Gb) for genotyping applications than whole genome sequencin...
© American College of Medical Genetics and Genomics ORIGINAL RESEARCH ARTICLE Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development Carin L. Yates, MS, Kristin G. Monaghan, PhD, Deborah Copenheaver, MS, Kyle Re...
Discover Almac's high-quality Whole Exome Sequencing (WES) service, built on Agilent’s chemistry with sequencing performed on the Illumina NovaSeq or NextSeq technology.
Data SetSequence TechnologyCoverageAssembly Time Yeast Genome (ERX009559)*Illumina22X2 Minutes Yeast Genome (srx1484451)*Ion Torrent22X3 Minutes Drosophila Genome (SRX1961013)*Illumina23X23 Minutes Human Exome (SRR701474)*Illumina81X53 Minutes ...