NX GEN WHOLE EXOME SEQUENCING
Whole exome sequencing (WES) is a genetic test to identify heritable cause of a disorder. WES searches through all the coding regions of the gene (exome) to identify variants. Human exome represents less than 2% of the genome but contains 85% of known disease related variants. This test is useful for the genetic analysis when patient presents with mutations in several genes which may have similar clinical presentation eg. neuropathies, ataxia, muscular disorders, skin disorders & thrombocytopenia. It is also useful when phenotype is atypical or combination of symptoms does not provide a definite diagnosis.
Parameter(s) covered : 2
Report Frequency: Sample Daily by 9 am; Report 30 Working days
Special Instruction: Duly filled Nx Gen Sequencing (NGS) Test Requisition Form (Form 40) is mandatory.
Price : ₹ 32400.00
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- NX GEN WHOLE EXOME SEQUENCING - THERMOFISHER