{"id":345,"date":"2020-08-31T11:32:25","date_gmt":"2020-08-31T11:32:25","guid":{"rendered":"https:\/\/genes2me.com\/blog\/?p=345"},"modified":"2020-08-31T11:32:28","modified_gmt":"2020-08-31T11:32:28","slug":"whole-exome-sequencing-genetic-testing-lab-in-india","status":"publish","type":"post","link":"https:\/\/genes2me.com\/blog\/2020\/08\/31\/whole-exome-sequencing-genetic-testing-lab-in-india\/","title":{"rendered":"Whole Exome Sequencing – An extensive cost effective genetic testing technology offering high diagnostic yield with accuracy"},"content":{"rendered":"\n
\"\"
Whole Exome Sequencing<\/figcaption><\/figure>\n\n\n\n

Whole Exome Sequencing<\/strong> (WES<\/strong>): <\/h2>\n\n\n\n

A comprehensive approach to the detection of disease-causing mutations present in the exome of an individual. Exome covers the protein-coding region of the genome; also called exons. Most of the genes responsible for any genetic abnormality and chromosomal disorder in a suspected individual are located in the exons. Sequencing of all the exons can help in identification of genetic cause behind the symptoms and signs observed in an individual. WES, an approach based on Next Generation Sequencing<\/a><\/strong>, is used for the detection of germline mutations located in the exome of an individual. Simultaneous screening of all the exons is an important aspect associated with this technique. <\/p>\n\n\n\n

Need of Whole Exome Sequencing<\/strong>:<\/h2>\n\n\n\n

The information obtained from targeted genetic testing technologies may not be sufficient to find the root cause behind the observable symptoms and signs in an individual. In such cases, diagnosis<\/strong> is delayed, which may have a severe impact on the medical health and treatment of an individual. WES is preferred in such specific cases as it screens all the exons of the genome for potential disease-causing mutated genes<\/strong>. Whole-exome sequencing genetic test diagnose single nucleotide variations and insertions and deletion of several sequences by default with high sensitivity and accuracy.\u00a0\u00a0 <\/p>\n\n\n\n

\"\"
Clinical Exome<\/figcaption><\/figure>\n\n\n\n

Sampling and Methodology<\/strong>:<\/h2>\n\n\n\n

The blood sample is acquired from the suspected individual and is sent to the processing laboratory for further analysis. Genomic DNA is isolated from the blood and is used for Whole Exome testing procedure. Further procedures are based on Next Generation Sequencing (NGS)<\/a><\/strong> platform. The data generated by NGS is aligned and analyzed for variations present in different gene sequences. <\/p>\n\n\n\n

Advantages of Whole Exome Sequencing<\/strong>:<\/h3>\n\n\n\n

This methodology offers complete genetic coverage of\nall the exons with sequencing depth > 100x. The test provides 97-99%\naccurate and reliable results about an unknown genetic condition. The results\ncan help in risk assessment of different family members pertaining to that\nspecific genetic condition. Analyzing the results can help the doctors in\nmanagement and designing specific medication for suspected disease identified. <\/p>\n\n\n\n

Genes2Me for WES<\/strong>:<\/h3>\n\n\n\n

Genes2Me<\/a><\/strong> Whole-exome test offers exceptional sensitivity and uniform exon coverage (covering approximately 22,000 genes). The test also uses the latest Next Generation Sequencing platform for processing the samples. Pre and post genetic counselling sessions are also provided for better interpretation of results along with the benefits associated with WES. The results obtained are also confirmed with Sanger sequencing. The results of the WES test can be obtained within 5-6 weeks. Doubtful of a suspected genetic condition and not getting informative results from regular targeted genetic tests. Go for Genes2Me WES!\u00a0\u00a0 <\/p>\n","protected":false},"excerpt":{"rendered":"

Whole Exome Sequencing (WES): A comprehensive approach to the detection of disease-causing mutations present in the exome of an individual. Exome covers the protein-coding region…<\/p>\n","protected":false},"author":1,"featured_media":346,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[5,6,50],"tags":[49,48,45,46,43,44],"yoast_head":"\nWhole Exome Sequencing Genetic Testing Cost in Delhi Gurugam India<\/title>\n<meta name=\"description\" content=\"Whole Exome sequencing is a featured genetic test that is being offered by selected genetic diagnostic companies in the country. 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Built on a strong foundation of scientific excellence and precision engineering, Genes2Me develops and manufactures advanced diagnostic technologies that enable accurate, reliable, and timely clinical decision-making across diverse healthcare settings worldwide. With a comprehensive and rapidly expanding portfolio, Genes2Me offers cutting-edge solutions across molecular diagnostics, including Next Generation Sequencing (NGS) clinical assays, point-of-care (POC) testing platforms, RT-PCR kits and instruments, as well as nucleic acid extraction kits and automation systems. Designed to meet the evolving needs of modern laboratories and clinicians, our products combine performance, scalability, and operational efficiency. A vast majority of Genes2Me products are CE-IVD marked, reflecting our commitment to global quality benchmarks, regulatory compliance, and uncompromising product standards. 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