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Prenatal Diagnostics | Sengenics
http://www.sengenics.com/doctors/prenatal-diagnostics
Pioneering Genomics in Diagnostics and Discovery. Full Range of Non-invasive Prenatal Tests. Non-invasive tests are safe for the mother and the foetus as only a sample of maternal blood is required. The key non-invasive tests offered by Sengenics are carried out in partnership with Sequenom:. MaterniT21 Plus – Sequenom – Non-invasive pre-natal Down’s Syndrome Trisomy Ch 13 and Ch 18 Test Y Chromosome ESS microdeletions. THE ENHANCED SEQUENCING SERIES, EXCLUSIVELY FOR THE MATERNIT21 PLUS TEST. Test covers...
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Why Test? | Sengenics
http://www.sengenics.com/doctors/why-test
Pioneering Genomics in Diagnostics and Discovery. Towards a Longer and Healthier Future. Sengenics offers 2 types of genetic tests:. Type 1 – For understanding your risk of developing a certain disease later in life. Type 2 – For accurate diagnosis of an existing or suspected disorder. Type 1 – Understanding your risk. Understand your risk even before you have symptoms. Get motivated and make changes to your diet and lifestyle based upon firm evidence. The breadth, accuracy and sensitivity of the Sengeni...
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99.7% Accurate Test for Down’s Syndrome | Sengenics
http://www.sengenics.com/individuals/mothers-downs-syndrome
Pioneering Genomics in Diagnostics and Discovery. 997% Accurate Test for Down’s Syndrome. Non-invasive Test for Trisomy 21, 18 and 13 Sex of baby 9 other syndromes. A non-invasive blood test for specific chromosomal abnormalities is available as early as 10 weeks in pregnancy. Sample is taken from mother’s blood, not from the womb. It’s your pregnancy. Demand the accuracy of the MaterniT21TM PLUS Test. No confusion. Just simple, clear results. Even more answers are now available. Your health care provide...
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About Us | Sengenics
http://www.sengenics.com/about-sengenics
Pioneering Genomics in Diagnostics and Discovery. Sengenics is a genomics- and proteomics-based research and diagnostics services company, with a range of patented technologies and products that are marketed to pharmaceutical companies, scientists and hospitals. It also has additional patented and proprietary products for Human diseases that use the GalaxC , ThalaSURE and Genoverse brand names. The three key focus areas for the company are:. 1 Proteomics based Research Services. With extensive experience...
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Clinical Exome Sequencing | Sengenics
http://www.sengenics.com/doctors/developmental-delay-test/whole-exome
Pioneering Genomics in Diagnostics and Discovery. Comprehensive Cost-effective CLIA Certified Sequencing. Sengenics has a panel of more than 80 certified MD/Clinical Geneticists from the US, UK and Holland,. With extensive experience in clinical exome interpretation. All clinical exome diagnosis reports are co-signed by two accredited panel members. Key applications of our Clinical Exome Sequencing service include diagnosis of:. The 5 key advantages of our service are:. Types of Clinical Report. Health a...
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Non-invasive Down Syndrome | Sengenics
http://www.sengenics.com/doctors/prenatal-diagnostics/sequenom-non-invasive
Pioneering Genomics in Diagnostics and Discovery. The MaterniT21 PLUS and VisibiliT tests are laboratory-developed tests that were developed, validated and performed exclusively by Sequenom Laboratories in the USA. Sequenom Laboratories is certified under the U.S. Clinical Laboratory Improvement Amendments (CLIA) as qualified to perform high complexity clinical laboratory testing and accredited by the College of American Pathologists (CAP). Want to know common genetic information. While results of this t...
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Why Test? | Sengenics
http://www.sengenics.com/individuals/why-test
Pioneering Genomics in Diagnostics and Discovery. It’s your pregnancy. Demand the accuracy of the MaterniT21TM PLUS Test. No confusion. Just simple, clear results. Even more answers are now available. Some people are born with an extra or missing chromosome, meaning they have three copies of a chromosome instead of two. This is known as a trisomy. The most common fetal trisomies are trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome) and trisomy 13 (Patau syndrome). Beyond whole chromosome changes.
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Portal | Sengenics
http://www.sengenics.com/portal
Pioneering Genomics in Diagnostics and Discovery. Download and manage Sengenics diagnostics reports, forms and technical information. Access reports quickly and conveniently from any location. Create Your Account Here. E-mail (must be from an institution). Located at the top right. Gene by Gene Diagnostics. Non Invasive Pre-natal Tests. PGD and IVF Screening. Full List of Tests. Health and Wellness Products. Heart and Stroke Risk.
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Cancer Diagnostics | Sengenics
http://www.sengenics.com/doctors/cancer-diagnostics
Pioneering Genomics in Diagnostics and Discovery. Exome, Array and Single-gene Cancer Diagnostics. 8220;The incorporation of whole-genome and whole-exome sequencing into clinical practice will undoubtedly change the way genetic counselors and other clinicians approach genetic testing. Enabling the analysis of essentially all human. Genes in one comprehensive test, this new technology can result in reduced testing cost and time to diagnosis (O’Daniel et al, Cancer J. 2012 Jul;18(4).”. 10 second - 1 click.
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Events | Sengenics
http://www.sengenics.com/sengenics-events
Pioneering Genomics in Diagnostics and Discovery. 13-14 October 2015 –. 5th Next Generation Sequencing Asia Congress & 3rd Single Cell Analysis Asia Congress, Singapore. 27 -29 July 2016 –. Immunoproteomics Symposium, Brunei Darussalam. Click this link for more information. Gene by Gene Diagnostics. Non Invasive Pre-natal Tests. PGD and IVF Screening. Full List of Tests. Health and Wellness Products. Heart and Stroke Risk.
