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The selective capture and sequencing of coding regions in the genome is a powerful and cost effective tool for researchers wanting to identify disease-causing mutations. Ambry Genetics has extensive experience with exome sequencing in both a research and clinical setting. As early adopters of NGS technology and advanced target enrichment techniques, Ambry’s experience and knowledge is hard to beat. Ambry was the 3rd Certified Service Provider (CSPro) lab in the world for Illumina NGS sequencing and 1st in the world for Agilent SureSelect Target Enrichment. In 2011, Ambry was the first company to offer CLIA-approved Whole Exome Sequencing for clinical diagnostics.
A1-hour discussion of the role both clinical aCGH and exome sequencing play in the optimization of genetic diagnosis. The purpose of this webinar is to discuss the unique roles of microarray and diagnostic exome sequencing in the clinical diagnostic process, while also examining benefits, limitations, and detection rates of these tests.
Amy Clugston, President of SWAN USA, gives us a look into her personal journey with undiagnosed disorders ever since her daughter was born with unexplained physical and developmental challenges. Amy started SWAN for other families facing similar challenges and needs, and has reached the hearts of thousands of families worldwide. Join us as Amy speaks to us about her and her daughter’s own diagnostic odyssey.
PancNextTM is a next-generation sequencing (NGS) panel that simultaneously analyzes 13 genes implicated in hereditary pancreatic cancer.
Utilizing next-generation sequencing (NGS) technology, Ambry Genetics developed a comprehensive test for hereditary pancreatic cancer (specifically pancreatic adenocarcinoma) comprised of 13 genes (APC, ATM, BRCA1, BRCA2, CDKN2A, EPCAM, MLH1, MSH2, MSH6, PALB2, PMS2, STK11, TP53).
RenalNext is a next-generation sequencing (NGS) panel that simultaneously analyzes 18 genes implicated in hereditary renal cell carcinoma.
Utilizing next-generation sequencing (NGS) technology, Ambry Genetics developed a comprehensive testing panel for hereditary renal cell carcinoma comprised of 18 genes (EPCAM, FH, FLCN, MET, MITF, MLH1, MSH2, MSH6, PMS2, PTEN, SDHA, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL).
OvaNext is a next generation (next-gen) sequencing panel that simultaneously analyzes 23 genes that contribute to increased risk for breast, ovarian and/or uterine cancers.
Ambry utilizes next generation sequencing to offer a comprehensive genetic testing panel for hereditary gynecologic cancers (cancer of the breast, ovary and/or uterus), including BRCA1 and BRCA2.
Producing music can be done many ways these days, some more, some less traditional. London-based acoustic bassist, pianist and percussionist Mark Bryan is making music in a unique way ... . Mark has created an impressive following via his Soundcloud music profile which showcases his memorable and varietal collection of music tracks - many that sound to be recording studio productions - but all of which were produced with an iPhone and a virtual music production application called NanoStudio. NanoStudio combines sampling, synthesis, sequencing and mastering. We discuss Mark's musical journey as a songwriter, musician and producer, learn more about virtual music production and discuss his mastery with music-making using NanoStudio.
Visit Mark at The Blue Room music profile.
CancerNext-ExpandedTM is a next generation sequencing (NGS) panel that simultaneously analyzes 43 genes associated with increased risk for breast, colon, ovarian, pancreatic, renal, uterine, and many other cancers. Ambry utilizes next-generation sequencing to offer a comprehensive hereditary pan-cancer panel.
PGLNext is a next-generation sequencing (NGS) panel that simultaneously analyzes 10 genes associated with an increased risk of developing paragangliomas and/or pheochromocytomas (PGL/PCC).
Utilizing next-generation sequencing (NGS) technology, Ambry Genetics developed a comprehensive testing panel comprised of 10 genes implicated in PGL/PCC susceptibility (MAX, NF1, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127, VHL).
An overview of Ambry's revolutionary form of genetic testing which allows scientists to diagnose many different diseases using far less tests than before. Scientists can now diagnose multiple different diseases with far fewer tests, easing the burden on patients and their families both emotionally as well as financially.
CONSPIRACIES AGAINST THE PEEPLE
A DECEIT that runs DEEP is going on in order to keep the MINDS of the PEEPLE ASLEEP and OBEYING all of these WORLD GOVERNMENTS. And this program Discusses and De-Codes how THIS IS constantly DONE thru mediums such as Movies, Music, News, Social Media and The Internet in general. We DE-CODE this MADNESS of POP CULTURE for Its TRUE meaning and apply that meaning to our World-At-Large to uncover Conspiracies as well as to De-Bunk Conspiracies while minimizing Fear Mongering.
We will be Covering such areas as Conspiracies, The Fukishima Hoax, The Global Warming Hoax, 9/11, Paranormal Phenomena, Parallel Universe, Lone Gunman Shootings, Assassinations, The Fake Financial/Currency Collapses, the Tracking of New Diseases n Pandemics. Also discussed will be Evidence of the ALIENS among us, Advanced Ancient technology/civilizations, Dark Matter, Cosomology, Teleportation, Time Travel, Transmorgrification, Parallel Universe, Wormhole, Nanotechnology, Neuroscience, Hive Mind, Subtle Bodies, Precognition, Cybernetics, UFO research, geopolitical developments and emergent energy technologies, Artificial Intelligence, Suspended Animation, complementary and alternative medicine, Surveillance Techniques/NSA, CIA, FBI, NASA Coverups, Black Ops, MK-Ultra, Manchurian Candidates, X-Files, Twilight Zone, Kolchak, Star Trek, Operation Paperclip and more!
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