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In newborns just got easier. A medically actionable genomic profile for. Hundreds of neonatal and pediatric inherited. Non-invasive and done in time. Used when a timely diagnosis is critical to. Have a team of rare disease experts. Interpretation of novel mutations that is easy. The Next Generation In Neonatal Diagnostics and Second Tier Testing. Is a rapid less-invasive method for sample collection and diagnosis of genetic conditions in neonates. Uncovering Genetic Causes of Disease. Answers On The Spot.

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In newborns just got easier. A medically actionable genomic profile for. Hundreds of neonatal and pediatric inherited. Non-invasive and done in time. Used when a timely diagnosis is critical to. Have a team of rare disease experts. Interpretation of novel mutations that is easy. The Next Generation In Neonatal Diagnostics and Second Tier Testing. Is a rapid less-invasive method for sample collection and diagnosis of genetic conditions in neonates. Uncovering Genetic Causes of Disease. Answers On The Spot.

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Home | Parabase Genomics | parabasegenomics.com Reviews

https://parabasegenomics.com

In newborns just got easier. A medically actionable genomic profile for. Hundreds of neonatal and pediatric inherited. Non-invasive and done in time. Used when a timely diagnosis is critical to. Have a team of rare disease experts. Interpretation of novel mutations that is easy. The Next Generation In Neonatal Diagnostics and Second Tier Testing. Is a rapid less-invasive method for sample collection and diagnosis of genetic conditions in neonates. Uncovering Genetic Causes of Disease. Answers On The Spot.

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blog.parabasegenomics.com

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Put your awesome Headline here. Follow you awesome headline with some supporting text. Maybe even write a couple lines of text here. This is where you explain a key benefit. Of your product or service. Another really good reason to use your service goes right here. Ought to be enough to sell anyone. Add another reason to buy right here. Here is a headline for another awesome offer! Welcome to the Business Theme. Awesome bullet goes here. Awesome bullet goes here. Awesome bullet goes here. When the Target...

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parabasegenomics.com

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Careers | Parabase Genomics

http://www.parabasegenomics.com/careers

We are looking for talented contributors who share our passion and want to be at the forefront of transforming inherited disease testing. Parabase Genomics is an Equal Opportunity Employer (EOE). We offer competitive salary or wages commensurate with experience and qualifications. If you would like to be considered for a position at Parabase Genomics, please submit your resume via email to careers@parabasegenomics.com. 27 Drydock Ave, 2. Boston, MA 02210. Need to move #precisionmedicine. 2 weeks 5 days.

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Search Gene Lists | Parabase Genomics

http://www.parabasegenomics.com/gene-table

11-beta-hydroxylase-deficient congenital adrenal hyperplasia. 17-alpha-hydroxylase-deficient congenital adrenal hyperplasia. 17-beta-hydroxysteroid dehydrogenase X deficiency (2-methyl-3-hydroxybutyric aciduria). 2,4-dienoyl-CoA reductase deficiency. 3-beta-hydroxysteroid dehydrogenase-deficient congenital adrenal hyperplasia. 3-Hydroxy-3-methylglutaryl-CoA synthase 2 deficiency. 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency. AUH, DNAJC19, OPA3. Acyl-CoA dehydrogenase 9 deficiency.

3

Request Kits Optimized for Neonates | Parabase Genomics

http://www.parabasegenomics.com/request-kits-optimized-neonates

Request Kits Optimized for Neonates. We know the challenges of obtaining blood from small babies so we have optimized our kits to support the collection of small volumes of blood on standard Spot Saver cards (Dried Blood Spots) as well as whole blood and saliva. If you require the shipment of other sample types or if you require samples to be shipped from outside the United States, please contact our Client Services group at 857.288.0838 or clientservices@parabasegenomics.com. 27 Drydock Ave, 2.

4

Patients | Parabase Genomics

http://www.parabasegenomics.com/patients

Ending a Diagnostic Odyssey. With our approach, healthcare providers can evaluate genes that are related to hundreds of conditions all at once instead of testing one at a time as was commonly done in the past. We believe the NewbornDx and RareDx tests will help shorten the time to a diagnosis, aid in medical management of patients, assist in family counseling, and provide possible therapeutic interventions. RareDx and NewbornDx Tests. Letter for Your Physician. What is Postnatal Genetic Testing? When to ...

5

Clinicians | Parabase Genomics

http://www.parabasegenomics.com/physicians

Ending the Diagnostic Delay. Test is designed to address multiple genetic conditions that may present in the newborn period, many of which have overlapping phenotypes and immediate implications for the newborn's treatment. It allows a clinician to utilize one test to provide an accurate molecular profile of 544 newborn-related genes using dried blood spots, run in trios, with results within 7-10 days. Newborn or infant with:. One or more of the features listed above*. Parents (if available): Whole blood.

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Product Variation 2

http://blog.parabasegenomics.com/products/product-1/variation-2

Enter your page name. Matching Newborns to Rare Therapeutics. Pressure BioSciences to Develop Front-end Sample Preparation for Parabase Genomics’ Targeted Next Generation Sequencing Testing Platform. When the Target Market is Right, Prognosis for Diagnostic Start-Ups is Bright. Limitations of Hearing Loss Testing in Newborns. About The Business Theme. Monthly Newsletter Sign Up. Sign up to revieve our monthly newsletter filled with awesome news about our super products and solutions. Business Theme, Inc.

blog.parabasegenomics.com

When the Target Market is Right, Prognosis for Diagnostic Start-Ups is Bright

http://blog.parabasegenomics.com/blog/prognosis-for-diagnostic-start-ups-is-bright

When the Target Market is Right, Prognosis for Diagnostic Start-Ups is Bright. Mar 27, 2014 10:49:00 PM. Gabor Bethlendy, Rina Wolf, and Arindam Bhattacharjee, PhD. Gabor Bethlendy and Arindam Bhattacharjee, Parabase Genomics, Boston, MA, USA. Rina Wolf, XiFin,. San Diego, CA. That gravy train is going to take a severe slow down in the coming years as it forces hospitals into Accountable Care Organizations. While it is true there have been some reports from SVB. Specifically, when it comes to recessive d...

blog.parabasegenomics.com

Management Team

http://blog.parabasegenomics.com/about-us/management-team

Enter your page name. Matching Newborns to Rare Therapeutics. Pressure BioSciences to Develop Front-end Sample Preparation for Parabase Genomics’ Targeted Next Generation Sequencing Testing Platform. When the Target Market is Right, Prognosis for Diagnostic Start-Ups is Bright. Limitations of Hearing Loss Testing in Newborns. About The Business Theme. Monthly Newsletter Sign Up. Sign up to revieve our monthly newsletter filled with awesome news about our super products and solutions. Business Theme, Inc.

blog.parabasegenomics.com

Pressure BioSciences to Develop Front-end Sample Preparation for Parabase Genomics’ Targeted Next Generation Sequencing Testing Platform

http://blog.parabasegenomics.com/blog/pressure-biosciences-to-develop-front-end-sample-preparation-for-parabase-genomics’-targeted-next-generation-sequencing-testing-platform

Pressure BioSciences to Develop Front-end Sample Preparation for Parabase Genomics’ Targeted Next Generation Sequencing Testing Platform. Jul 22, 2014 12:58:00 PM. Initial Target of the Parabase Sequencing Service are the Neonatal Intensive Care Units of. US Hospitals with a Goal of Improving the Early Diagnosis of Genetic Diseases. South Easton, MA, July 22, 2014 Pressure BioSciences, Inc. (OTCQB: PBIO) ( PBI or the Company ) and Parabase Genomics. Unfortunately, it is difficult to diagnose genetic dise...

blog.parabasegenomics.com

Limitations of Hearing Loss Testing in Newborns

http://blog.parabasegenomics.com/blog/misconceptions-about-hearing-loss-testing-in-newborns

Limitations of Hearing Loss Testing in Newborns. Mar 7, 2014 12:33:30 AM. Newborn hearing screening has positively affected childhood developmental outcomes. However, limitations remain, including;. High false positive and negative rates of detection for progressive and late onset deafness. Multi-tiered testing is routinely required as symptoms develop. There is no focus on differentiating non-genetic causes, genetic predisposition to ototoxic drugs, and genetic causes of hearing loss. The costs associat...

blog.parabasegenomics.com

Matching Newborns to Rare Therapeutics

http://blog.parabasegenomics.com/blog/matching-newborns-to-rare-therapeutics

Matching Newborns to Rare Therapeutics. Jan 14, 2015 4:02:31 PM. While many people have heard about Newborn Screening I imagine few have heard about neonatal diagnostics. That's because most are waiting for the costs of next gen sequencing to come down before population wide "screening" could begin at an affordable rate since screening is paid for from public funds. Here is a video that shows you how we could do this now and not get stuck focused on the costs;. Why are NICUs not using such a test? We are...

undiagnosed-usa.org

Exome Sequencing

http://www.undiagnosed-usa.org/globalgenes.htm

Exome Sequencing Give Away. Global Genes has partnered with SWAN USA to provide Undiagnosed Rare Disease Patients an opportunity for Free Whole Exome Sequencing. Global Genes Undiagnosed Patient Program started from their first fundraising appeal at their Second Annual Tribute to Champions of Hope on September 21, 2013. Soon after they put together an advisory board to help move this program forward. SWAN USA's founder and president, Amy Clugston is part of the advisory board. PR Newswire . Go to.

geneticobesity.com

Find a Diagnostic Testing Lab - The Genetic Obesity ProjectThe Genetic Obesity Project

http://geneticobesity.com/resources/diagnostic-testing-pomc-lepr-deficiency

About the Genetic Obesity Project. About Rare Genetic Disorders of Obesity. About the MC4 Pathway. Find a Treatment Referral Center. Find a Diagnostic Testing Lab. Patients & Healthcare Professionals:. Join the effort to identify people. I am a Healthcare Professional. I am a Patient or Caregiver. Find a Diagnostic Testing Lab. Find a Treatment Referral Center. Find a Diagnostic Testing Lab. Find a Diagnostic Testing Lab. Baylor Miraca Genetics Laboratories. POMC, PCSK1, LEPR. Test codes: 6860, 6861).

sxeventures.com

Portfolio — SXE VENTURES

http://www.sxeventures.com/portfolio

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Home | Parabase Genomics

In newborns just got easier. A medically actionable genomic profile for. Hundreds of neonatal and pediatric inherited. Non-invasive and done in time. Used when a timely diagnosis is critical to. Have a team of rare disease experts. Interpretation of novel mutations that is easy. The Next Generation In Neonatal Diagnostics and Second Tier Testing. Is a rapid less-invasive method for sample collection and diagnosis of genetic conditions in neonates. Uncovering Genetic Causes of Disease. Answers On The Spot.

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