Author name: Scott Sounder

Detecting the Variation in the Exome Sequence

The clinical exome testing in a targeted DNA test helps with the identification of genetic disorders in humans caused due by exome sequence or gene variation. As 85% of the disease-causing variants are present with the 1% of the exome comprising the exons and splice junction, it helps in identifying the pre-disposition of genetic disease. The clinical exome […]

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Find the Most Affordable Clinical Exome Sequencing Test Price in India

Indian clinical exome sequencing cost in the current scenario is very much cheaper than clinical sequencer in Europe and United States. According to reports, Indian clinical exome sequencing cost in current scenario is just half that of clinical exome sequencing cost in Europe and United States. With the advent of new technologies and introduction of

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Whole Exome Sequence – Detecting Changes within the Exon for Diagnosing Genetic Disease

Understanding the Genome and Relevance of Exome  The genome consists of the genetic material and in humans; the introns are spliced out to form an exome which consists of only the exons. The whole exome chromosomal microarray test help with prenatal analysis for the presence of any chromosomal aberration in the growing fetus. The chromosomal microarray helps

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RTPCR – A Real-Time Detection of Virus through Viral Genetic Material Amplification

COVID-19 has traumatized people from across the globe and initially, it was chaos handling the novel virus. However, with time the RT PCR test provided the much-needed respite by accurate diagnosing if an individual has contracted the coronavirus. The technology dwells on the power of real-time PCR for the detection of the presence of the genetic material

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Microarray Analysis – A Comprehensive Screening to Detect Copy Number Variants and Chromosome Abnormality

It is a crucial prenatal screening test to determine the presence or absence of chromosomal aberration in the growing fetus. The presence of such chromosomal abnormality in the mother or the fetus is one of the most common causes for recurrent miscarriages in a woman. The high-resolution technology helps in screening for microdeletion or addition

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Hereditary Cancer – BRCA Comprehensive Testing to Screen for Mutations and Variations

One of the most common inherited gene variants causing pre-disposition of cancer is the BRCA mutant. The genetic variants of genes are harmful as it tends to form cancer or develop other diseases. One of the common genetic variants that can cause breast, ovarian and prostate cancer is the BRCA gene mutation. BRCA Variation –

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