Whole Exome Sequencing Panel TWES is usage of NGS sequencing technology for the diagnosis of diseases causing variants in entire protein coding regions or exomes in the human genome corresponding to >19000 genes. WES covers more than 95% of the exons, which contains 85% of disease-causing mutations in Mendelian disorders and many disease-causing SNPs throughout the genome. It helps in correct diagnosis of rare genetic disorders and syndromes for which no etiology is known.
Genes2Me Whole Exome Sequencing (WES) Panel is a comprehensive solution that covers all target regions of major WES panels available in the market. With a target size of 37.1 Mb, the panel does not compromise performance in terms of coverage and uniformity. It enables highly efficient and cost-effective sequencing of the human whole exome. The panel coverage spans across exon regions from RefSeq, CCDS, and GENCODE.
WEB panel shows exceptional performance for parameters like on-target read ratio, 0.2x mean depth coverage uniformity, and Fold-80 base penalty.