#exome sequencing

Lipodystrophy is a term that refers to a group of disorders in which our body fails to produce fat (total fat loss) or abnormally accumulates fat. It can be both congenital or acquired & partial or generalised. This condition is usually manifested with other metabolic abnormalities normally related with Diabetes, PCOS, hypertriglyceridemia. Lipodystrophy are of many types but when present in generalised congenital form, it is presented very severely and mostly inherited in autosomal recessive manner. If presented in partial form, it can be inherited in an autosomal dominant manner too. Exome Sequencing can help in identification of mutated genes responsible for this heterogeneous condition. Know more about Exome Sequencing with Genes2Me #WorldLipodystrophyDay #liposydtrophy #exomesequencing #adiposetissue #diagnostic #familial #healthcare #health #skincare

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Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data. Veatch, et al., Journal of neurodevelopmental disorders doi: 10.1186/s11689-022-09448-8.

Whole-exome sequencing is the next-generation sequencing (NGS) method that is utilised to sequence the protein coding regions of the genome. Using exome enrichment, exome sequencing can efficiently identify coding variants across a broad range of applications, including population genetics, genetic disease, and cancer studies. Uncover any rare abnormality with the help of exome sequencing. Call US on 18001214030 or drop us an email at [email protected] for an Appointment.

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Exome sequencing is a type of genetic sequencing increasingly used to understand what may be causing symptoms or a disease. Exome Sequencing has proven exceptionally useful for molecular diagnosis of rare monogenic disorders, identification of complex phenotypes, and tumor/normal analysis to identify driver genes in cancer. Take the Genes2Me test to get better understanding of rare inherited diseases.

Call US on 18001214030 or drop us an email at [email protected] for an Appointment. To know more visit. cutt.ly/uWqJEOw #Sequencing #Exome #ExomeSequencing #GenomeSequencing #Diagnosis #GeneticDisorders #ClinicalStudy #Sequence #TestingServices #Genes #GeneticTesting #Genetics #AntibodyTesting #HealthCare #Health

Clinical Exome Sequencing is a test used to identify disease-causing DNA variants within the 1% of the genome, which codes for proteins (exons) or flanks the regions that code for proteins (splice junctions).  The genetic test results can help you confirm or rule out a suspected genetic condition or help determine your chance of developing or passing on a genetic disorder. Book the test at [email protected] and call us on 18001214030 for exemplary service. To know more visit. cutt.ly/Kmna6Qg #cancercare #clinicallaboratory #clinicaldiagnostics #sequencing #sequence  #DNA #DNASequencing #GeneticTesting #Genetics #Antibodies #AntibodyTest #AntibodyTesting #COVIDAntibodiTest #COVID #Pendamic #Immunity #COVIDAntibodyTest #RTPCRTest #RTPCR

Sequencing helps to detect changes in DNA responsible for various diseases. Whole Exome Sequencing (WES) sequences all genes that code for our proteins. Its application is increasing in personalized medicine. Nowadays WES is being widely used in areas like reproductive health, multifactorial diseases, cancer therapeutics and pharmacogenetics. WES covers approximately 22,000 genes. Explore the Exome Sequencing with #Genes2Me at the link mentioned in the bio. #Personalizedmedicine #Diagnostic #GeneticTesting

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Exome Sequencing is a highly advanced technique which analyses the protein-coding regions (exome) of your DNA. #ExomeSequencing test is available with #Genes2Me as #ClinicalExome Sequencing which analyzes your exome associated with known genetic disorders and #WholeExome Sequencing which analyses all the exome regions present in the whole genome. Exome Sequencing wirth #Genes2me includes #mitochondrial Genome coverage in the same test and helps in identification of rare genetic disorders.

#genetictesting #diagnostic #healthcare

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