Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest | |
Anonymous Coward User ID: 76942420 United States 07/26/2020 03:51 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (July 22, 2020) With eyes on reopening, some colleges turn to saliva coronavirus tests for students With demand for coronavirus testing expected to rise even higher this fall as students return to campuses across the nation, some major universities are adding their names to the list of those turning to at-home test kits that look for the virus in a person's saliva -- a novel technique that's raised hopes, and questions, when it comes to mass testing. “The current benefits outweigh the risks,” Purdue University Chief Medical officer Dr. Esteban Ramirez told ABC News. “The beauty of this is that we can screen and test everyone before they arrive on campus.” Purdue officials said they plan to test every one of their 40,000 students with saliva kits prior to the fall semester. [link to abcnews.go.com (secure)] |
Anonymous Coward User ID: 78617574 United States 07/26/2020 03:56 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest it'd be terrifying if that genetic information weren't useless. what percentage of its ancestry kits does 23andme sell to foreigners, this appears to be more like the type of product only the government is dumb enough to buy |
Anonymous Coward User ID: 77795952 Sweden 08/07/2020 03:04 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (August 5, 2020) Seven States Join Pact to Speed Coronavirus Testing Three Republican governors and three Democratic governors signed an interstate testing agreement on Tuesday, The New York Times reported. Louisiana, Maryland, Massachusetts, Michigan, Ohio and Virginia will work with the Rockefeller Foundation and two U.S. manufacturers of rapid tests to buy 3 million tests, the newspaper said. A seventh state, North Carolina, later joined the pact, CNN reported. The United States is testing about 755,000 people a day, up from about 640,000 per day a month ago, the Times reported. [link to www.usnews.com (secure)] |
Anonymous Coward User ID: 71612244 United Kingdom 08/10/2020 03:05 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (August 5, 2020) Seven States Join Pact to Speed Coronavirus Testing Quoting: Anonymous Coward 77795952 Three Republican governors and three Democratic governors signed an interstate testing agreement on Tuesday, The New York Times reported. Louisiana, Maryland, Massachusetts, Michigan, Ohio and Virginia will work with the Rockefeller Foundation and two U.S. manufacturers of rapid tests to buy 3 million tests, the newspaper said. A seventh state, North Carolina, later joined the pact, CNN reported. The United States is testing about 755,000 people a day, up from about 640,000 per day a month ago, the Times reported. [link to www.usnews.com (secure)] (August 5, 2020) Blackstone Reaches $4.7 Billion Deal to Buy Ancestry.com Blackstone Group Inc. acquired a majority stake in Ancestry.com Inc., the business known for family history research and DNA testing. It’s the first acquisition by Blackstone’s largest ever private equity fund. Silver Lake and Singaporean sovereign-wealth fund GIC Pte have been the majority owners since 2016. After the deal closes, Blackstone will own about 75% and GIC will still hold about 25% of Ancestry.com, said people familiar with the matter, who asked not to be identified because the information is private. Based in Lehi, Utah, Ancestry.com has more than 3 million paying subscribers and more than 18 million people in its DNA network. It sells at-home DNA testing kits to customers, competing with 23andMe Inc. [link to www.bloomberg.com (secure)] |
Anonymous Coward User ID: 41011373 United States 08/10/2020 03:09 PM Report Abusive Post Report Copyright Violation | |
Anonymous Coward User ID: 71617737 United Kingdom 08/15/2020 02:48 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (August 12, 2020) Alphabet’s Verily opens own lab to speed up COVID testing In a blog post, Verily, Alphabet's life sciences research arm and a sister company to Google, has set up its own CLIA-certified lab (i.e., it has clinical laboratory credentials) and used tech from Thermo Fisher Scientific’s‎ TaqPath test kit, which has an emergency use tag (EUA) from the FDA, to test for COVID-19. It’s also sent off an EUA application for an adaptation of the TaqPath test for use in testing pooled patient specimens, which can further speed up testing. And it’s “verified” the Roche Elecsys Anti-SARS-CoV-2 antibody test, which can assess if you’ve had the disease (rather than currently have it), with plans to “implement additional tests in our lab,” said Deb Hanks, M.D., lead pathologist at Verily, in the blog post. [link to www.fiercebiotech.com (secure)] |
Anonymous Coward User ID: 76319445 Netherlands 08/21/2020 01:34 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (August 15, 2020) FDA Issues Emergency Use Authorization to Yale School of Public Health for SalivaDirect, Which Uses a New Method of Saliva Sample Processing Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) to Yale School of Public Health for its SalivaDirect COVID-19 diagnostic test, which uses a new method of processing saliva samples when testing for COVID-19 infection. Yale intends to provide the SalivaDirect protocol to interested laboratories as an “open source” protocol, meaning that designated laboratories could follow the protocol to obtain the required components and perform the test in their lab according to Yale’s instructions for use. This is the fifth test that the FDA has authorized that uses saliva as a sample for testing. Testing saliva eliminates the need for nasopharyngeal swabs, which have also been prone to shortages, and alleviates the patient discomfort associated with these swabs. [link to www.fda.gov (secure)] |
Anonymous Coward User ID: 76319445 Netherlands 08/26/2020 03:18 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest GERMANTOWN, Md. & HILDEN, Germany--(BUSINESS WIRE)--QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced the U.S. launch of the new Access Anti-SARS-CoV-2 Total test, an easy-to-use digital test done on a portable device that provides results in about 10 minutes to detect antibodies in people exposed to the SARS-CoV-2 virus, which is the case of COVID-19. The launch of this antibody test, which was developed in partnership with the Australian digital diagnostics company Ellume, comes after the submission by QIAGEN of this unique antibody test to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA). First shipments are planned for late August 2020. A CE-IVD marking for Europe and other markets is planned in the coming weeks. The new serological test has been shown to have sensitivity of 100% (CI 88.43–100.00%) and specificity of 100% (CI 95.20–100.00%). The nanoparticle fluorescent detection technology uses serum or plasma from patient samples [link to www.businesswire.com (secure)] |
Anonymous Coward User ID: 77795952 Sweden 08/27/2020 05:34 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (August 25, 2020) Fluidigm Granted FDA Emergency Use Authorization for Saliva-Based Advanta Dx SARS-CoV-2 RT-PCR Assay for COVID-19 SOUTH SAN FRANCISCO, Calif., Aug. 25, 2020 (GLOBE NEWSWIRE) -- Fluidigm Corporation (Nasdaq:FLDM), an innovative biotechnology tools provider with a vision to improve life through comprehensive health insight, today announced it has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for the Advanta™ Dx SARS-CoV-2 RT-PCR Assay, an extraction-free saliva-based test to detect nucleic acid from the SARS‑CoV‑2 virus, designed to be run on the Fluidigm® Biomark™ HD microfluidics platform. The clinical study associated with the EUA submission demonstrated 100 percent agreement between the saliva results from the Advanta Dx SARS-CoV-2 RT-PCR Assay and the results from paired nasopharyngeal samples tested with authorized assays. The company’s microfluidics technology enables processing of more samples per batch than more traditional, microwell plate-based PCR technology. The Biomark HD platform can generate as many as 6,000 test results per day on a single system. Fluidigm was recently selected by the National Institutes of Health (NIH), National Institute of Biomedical Imaging and Bioengineering, for a proposed project under the agency’s Rapid Acceleration of Diagnostics (RADx) program. Fluidigm’s ongoing collaboration with the Defense Advanced Research Projects Agency (DARPA) and its Epigenetic CHaracterization and Observation (ECHO) program includes financial support for development of innovative programs based on our microfluidics technology. [link to www.globenewswire.com (secure)] |
Anonymous Coward User ID: 77940018 United States 09/13/2020 03:48 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (September 11, 2020) FDA grants EUA to Verily Life Sciences for COVID-19 test, pooling techniques The U.S. Food and Drug Administration (FDA) granted an emergency use authorization (EUA) to Verily Life Sciences, a subsidiary of Alphabet, for a RT-PCR test to detect SARS-CoV-2 as well as for a pooled sampling technique, according to an approval letter from the FDA. In its letter to Verily, the FDA said the EUA was for the qualitative detection of nucleic acid from SARS-CoV-2 in upper-respiratory specimens as well as for the pooled testing of up to 12 specimens collected by healthcare providers. Verily said it verified the performance of the RT-PCR test in its lab with Thermo Fisher Scientific’s‎ TaqPath test kit. Earlier this year, Verily also launched the Baseline COVID-19 testing program in conjunction with the state of California, as an integrated solution combining symptom reporting, specimen collection, testing and reporting of results. Since then, the program has expanded to other states, including Connecticut, Delaware, Idaho, Massachusetts, Maryland, Michigan, New Hampshire, New Jersey, New York, Ohio, Oregon, Pennsylvania, Virginia and Washington. [link to www.mlo-online.com (secure)] |
Anonymous Coward User ID: 76319445 Netherlands 09/23/2020 02:19 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (September 23, 2020) Privacy Fears Rising as DNA Test Companies Shift to New Ventures At-home DNA test kits from companies like 23andMe and Ancestry have enabled customers to trace their heritage and piece together family trees. A lack of strict data privacy protections has allowed these companies to rack up hundreds of millions in revenue through the collection of DNA samples and sales of genetic data, all with the consent of customers who may not have read the fine print. As it stands, there is no comprehensive federal privacy law in the U.S. Other laws, including HIPPA and the Genetic Information Discrimination Act, only keep genetic information off-limits to certain types of insurers and employers. Further, the agency that is supposed to enforce privacy rules by DNA testing companies, the Federal Trade Commission, has limited authority. Exposed genetic information poses risks from the mundane to the extreme, experts say. Long-term care, disability and life insurers, for example, can still legally inflate their rates based on a customer’s predisposition to adverse health conditions. And if a person takes a DNA test, the information could be used to profile unsuspecting relatives as well. Some have warned of more dire consequences. One DNA data security startup, Geneinfosec—which counts former U.S. assistant secretary of defense Andrew C. Weber among its advisors—claims that someone’s DNA profile could be used as blackmail, or even to create bioweapons that target specific people. In 2019, Pentagon officials advised military troops to avoid taking consumer DNA tests because they could, “create unintended security consequences and increased risk to the joint force and mission.” [link to www.fairwarning.org (secure)] |
Anonymous Coward User ID: 77435937 Netherlands 10/28/2020 03:45 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest During an interview with the Wall Street Journal published last Friday, the “captain” of Operation Warp Speed, career Big Pharma executive Moncef Slaoui, confirmed that the millions of Americans who are set to receive the project’s Covid-19 vaccine will be monitored via “incredibly precise . . . tracking systems” that will “ensure that patients each get two doses of the same vaccine and to monitor them for adverse health effects.” Slaoui also noted that tech giants Google and Oracle have been contracted as part of this “tracking system” but did not specify their exact roles beyond helping to “collect and track vaccine data.” The day before the Wall Street Journal interview was published, the New York Times published a separate interview with Slaoui where he referred to this “tracking system” as a “very active pharmacovigilance surveillance system.” [link to www.thelastamericanvagabond.com (secure)] (October 21, 2020) Stanford Medicine launches home COVID-19 testing study covering greater San Francisco Stanford University and its school of medicine have launched plans to survey the population of greater San Francisco for COVID-19, in an effort to build an early warning system for future outbreaks. The program is currently seeking to enroll participants, who will report their exposures and symptoms daily through an online portal. Home test kits—developed in collaboration with the Chan Zuckerberg Biohub, which is also helping to fund the study—will be delivered through the mail within 24 hours at no cost, and will contain a gentle nasal swab for self-collection. Samples will then be processed at Stanford’s laboratories. [link to www.fiercebiotech.com (secure)] |
Anonymous Coward User ID: 79417936 United Kingdom 11/04/2020 03:42 PM Report Abusive Post Report Copyright Violation | |
Anonymous Coward User ID: 79444432 Germany 02/07/2021 03:08 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (October 30, 2020) Verily's COVID-19 testing program halted in San Francisco and Oakland (Verily is a subsidiary of Google’s parent company Alphabet) In a June letter (PDF) to California Secretary of Health Mark Ghaly, Oakland Mayor Libby Schaaf and other members of the county’s COVID-19 Racial Disparities Task Force raised numerous concerns about the Verily protocols. Among their complaints: People signing up for a test through Verily had to do so online, using an existing or newly created Gmail account; the sign-ups were offered only in English or Spanish; and participants were asked to provide sensitive personal information, including their home address and whether they were managing chronic health conditions such as diabetes, obesity or congestive heart failure, which could expose their data to third-party use. Noha Aboelata, M.D., is CEO of Roots Community Health Center, an East Oakland clinic that serves mostly African Americans and is one of the original Verily sites in Oakland. Problems emerged almost immediately, she said. People were suspicious of the requirement that they sign up with a Gmail account and the request for personal information such as health status and risk factors. “You don’t necessarily want to share that with Google,” Aboelata said. Then there was the language in the privacy policy that allows for sharing data with third parties. The Roots line for clients who did not register through Verily, on the other hand, was made up mostly of people of color from the community who long had come to the clinic for medical care, she said. When Aboelata looked at the data, the disparities were obvious: 12.9% of people tested in the non-Verily line were positive for COVID-19, while just 1.5% of people tested in the Verily-registered line were positive. For Aboelata, it was clear that the two lines were testing two entirely different populations. After just six days of testing, Aboelata asked Verily to leave. [link to www.fiercebiotech.com (secure)] (December 4, 2020) New CRISPR-Based Test for COVID-19 Uses a Smartphone Camera In a new study published in the scientific journal Cell, the team from Gladstone, UC Berkeley, and UCSF has outlined the technology for a CRISPR-based test for COVID-19 that uses a smartphone camera to provide accurate results in under 30 minutes. The technique was designed in collaboration with UC Berkeley bioengineer Daniel Fletcher, PhD, as well as Jennifer Doudna, PhD, who is a senior investigator at Gladstone, a professor at UC Berkeley, president of the Innovative Genomics Institute, and an investigator of the Howard Hughes Medical Institute. Doudna recently won the 2020 Nobel Prize in Chemistry for co-discovering CRISPR-Cas genome editing, the technology that underlies this work. "When coupled with repeated testing, measuring viral load could help determine whether an infection is increasing or decreasing," says Fletcher, who is also a Chan Zuckerberg Biohub Investigator. [link to www.prnewswire.com (secure)] (December 28, 2020) 23andMe Raises More Than $80 Million in Equity Financing Round DNA testing company 23andMe Inc. raised more than $80 million in equity in a financing round led by Sequoia Capital and NewView Capital. According to Securities and Exchanges Commission filings, the company offered $85 million in equity and sold about $82.5 million. Previously, the company had raised about $791 million. In recent years, 23andMe has begun moving beyond telling individual consumers about their DNA and begun work developing therapeutics based on research into genetic information its customers provide. For example, the company has used its data to find genetic differences that can affect a person’s susceptibility to Covid-19. [link to www.bloomberg.com (secure)] |
Anonymous Coward User ID: 79444432 Germany 02/07/2021 03:08 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (January 23, 2021) OraSure’s Oragene Dx saliva collection kit included in industry’s first US FDA authorization for whole exome sequencing platform OraSure Technologies, a leader in point-of-care diagnostic tests, specimen collection devices, announced that its Oragene Dx (OGD-610) saliva collection device was included as a component in the De Novo authorization granted by the US Food & Drug Administration (FDA) to Helix for their Helix Laboratory Platform, a whole exome sequencing platform. This is the first exome sequencing-based platform authorized by the FDA. Oragene Dx is a product of OraSure’s DNA Genotek subsidiary. In 2020, Oragene Dx received US Food and Drug Administration (FDA) general use 510(k) clearance and remains the first and only device with general clearance for collection and stabilization of DNA from saliva for use in genetic testing, including prescription or over-the-counter (direct-to-consumer) use. Saliva samples collected using Oragene Dx are stabilized for use in downstream diagnostic testing applications and can be transported and/or stored long-term at ambient temperatures. [link to pharmabiz.com] (January 26, 2021) Chronomics selects OraSure's OMNIgene ORAL salive collection kit OraSure Technologies announced that Chronomics Limited has selected the OMNIgeneORAL saliva collection device as a component of its SARS CoV-2 PCR test. Chronomics Limited will supply its test for the United Kingdom's "Test to Release for International Travel" program. The OMNIgeneORAL device is a product of OraSure's DNA Genotek subsidiary. The "Test to Release for International Travel" program enables travelers to England to purchase a COVID-19 test privately from providers including Chronomics. Travelers who receive a negative test result can reduce their self-isolation period. The project is part of the UK's plan to use Covid-19 testing to reduce the spread of the virus. [link to thefly.com (secure)] (January 27, 2021) 23andMe in Talks to Go Public Via Branson SPAC Consumer DNA-testing company 23andMe Inc. is in talks to go public through a roughly $4 billion deal with VG Acquisition Corp., a special purpose acquisition company founded by billionaire Richard Branson, according to people familiar with the matter. Co-founded in 2006 by Anne Wojcicki, 23andMe sells direct-to-consumer genetic testing kits. The company launched with the aim of using genetics to kick start a personalized health-care revolution, with a $1,000 test that could alert customers to potential health risks. When the Covid-19 pandemic began last year, 23andMe launched a million-person study to look at how genomics and other factors contribute to how severely ill those who contract the virus become. 23andMe has raised $869 million in private funding to date and counts Sequoia Capital and Fidelity Management among its backers. [link to www.bloombergquint.com (secure)] |
REaliZe
User ID: 79267289 United States 02/07/2021 03:13 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest There's. A. H0le. In. The. Sky. |
Anonymous Coward User ID: 79444432 Germany 02/07/2021 03:28 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (February 1, 2021) Illumina, Sequoia Capital launch genomics startup incubator in China Illumina has partnered up with Sequoia Capital’s China-based subsidiary to launch a new incubator for genomics startups. Based in Shanghai, the project follows Illumina’s previous accelerator work with startups in the San Francisco and Cambridge, U.K., areas, as well as Sequoia Capital China’s incubation efforts focused on digital technologies. The program—officially dubbed the Sequoia Capital China Intelligent Healthcare Genomics Incubator, Powered by Illumina—is set to operate on six-month funding cycles with at least three startups selected at a time, and first participants will begin work this fall. [link to www.fiercebiotech.com (secure)] |
Anonymous Coward User ID: 79964128 Germany 02/12/2021 06:08 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (February 8, 2021) Verily links with Janssen for at-home COVID-19 immune system study Verily is teaming up with Johnson & Johnson’s Janssen division to observe the body’s earliest immune responses to a coronavirus infection, with people participating in the research from within their own homes. The study will be launched through Verily’s Project Baseline testing program and aims to collect biological information and real-world data in the weeks immediately after a person tests positive for COVID-19. Separately, Verily recently opened up its coronavirus-focused Project Baseline efforts to children as young as four, while pediatric testing and COVID-19 research has previously been limited. The program will offer free COVID-19 testing to children through 450 screening sites across 16 states. [link to www.fiercebiotech.com (secure)] |
Anonymous Coward User ID: 79955455 Italy 02/20/2021 03:45 PM Report Abusive Post Report Copyright Violation | Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest (February 19, 2021) Superdrug launches Covid-19 PCR saliva testing Superdrug has become the first high street retailer to offer a Chronomics Covid-19 PCR testing service that uses a patient’s saliva. The price covers the test as well 24 hour tracked return delivery of the test, analysis of the sample and the results being processed and eventually being returned to the customer. You should get your results within 36 hours of taking the test. At a recent Downing Street press conference the PM hinted mass deployment of saliva tests will play a fundamental part in rolling back lockdown restrictions on large events. [link to www.pharmacy.biz (secure)] [link to www.the-sun.com (secure)] |