Health & Safety

How to find the best topical formulation development company?

Finding the best nanoemulsionmicroFLuidization formulation is not an easy feat for the clients. There are however some factors to consider before selecting the best glp formulation company. Keeping these factors in mind is helpful when selecting the company for developing drugs. • The reputation of the company Check the reputation of the company. This will help […]

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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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Clinical Exome Sequencing – Identifying Underlying Genetic Disorders or Phenotypic Change Resulting from Exon Variation

The genome sequencing consists of exon and intron sequences but only the exons are spliced together to form genes that encode for various proteins. Any variation or mutation in the protein-encoding genes can result in genetic disorder, phenotypic change, or inherit the condition to the offspring. Clinical exome sequencing is a targeted and powerful diagnostic technique that

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Chromosomal Microarray – A Non-Invasive Technique for Identifying Chromosomal Aberrations in Fetus

Advanced technology has made it possible to screen the genetic sequence for the presence of any mutation and variation. With the growing awareness of genetic testing and its widespread benefits, it helps in screening for the presence of chromosomal aberrations and detecting the presence of any underlying genetic conditions. The cost of microarray genetic testing in

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BRCA Gene Testing – A Preventive Genetic Screening for Identifying Risk of Breast Cancer

Breast cancer is one of the most common forms of cancer in women but there is less awareness of it being an inherited cancer form. The BRCA1 and BRCA2 variants inherited from parents to offspring highly increase the risk of breast and ovarian cancer. Cancer gene testing helps in the early detection of BRCA1 and BRCA2 genes

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