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Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest

 
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Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest
(November 27, 2013) 23andMe Is Terrifying, but Not for the Reasons the FDA Thinks
While the FDA concentrates on the question of whether 23andMe’s kit
is a safe and effective medical device, it is failing to address the real issue:
what 23andMe should be allowed to do with the data it collects.
For 23andMe’s Personal Genome Service is much more than a medical device; it is a one-way portal
into a world where corporations have access to the innermost contents of your cells
and where insurers and pharmaceutical firms and marketers might know more about your body than you know yourself.
And as 23andMe warns on its website, “Genetic Information that you share with others could be used against your interests.
You should be careful about sharing your Genetic Information with others.”
[link to www.scientificamerican.com (secure)]

(January 6, 2015) Surprise! With $60 Million Genentech Deal, 23andMe Has A Business Plan
A deal being announced today with Genentech points the way for 23andMe,
the personal genetics company backed by Facebook billionaire Yuri Milner and Google Ventures
to become a sustainable business – even if the company’s discussions with the U.S. Food and Drug Administration stretch on for years.
Such deals, which make use of the database created by customers who have bought 23andMe’s DNA test kits and donated their genetic and health data
for research, could be a far more significant opportunity than 23andMe’s primary business of selling the DNA kits to consumers.
Since it was founded in 2006, 23andMe has collected data from 800,000 customers and it sells its tests for $99 each.
That means this single deal with one large drug company could generate almost as much revenue as doubling 23andMe’s customer base.
“I think that this illustrates how pharma companies are interested in the fact that we have a massive amount of information,” says Anne Wojcicki, 23andMe’s chief executive and co-founder.
Wojcicki and her husband Sergey Brin (the two are now separated) have been very public about their desire to understand Parkinson’s, which runs in Brin’s family.
[link to www.forbes.com (secure)]

(January 11, 2015) Live for ever: Scientists say they’ll soon extend life ‘well beyond 120’
Fixing the ‘problem’ of ageing is the mission of Silicon Valley, where billions is pouring into biotech firms working to ‘hack the code’ of life
– despite concerns about the social implications. In September 2013 Google announced the creation of Calico, short for the California Life Company.
Its mission is to reverse engineer the biology that controls lifespan and “devise interventions that enable people to lead longer
and healthier lives”. Though much mystery surrounds the new biotech company, it seems to be looking in part to develop age-defying drugs.
In April 2014 it recruited Cynthia Kenyon, a scientist acclaimed for work that included genetically engineering roundworms to live up to six times longer than normal,
and who has spoken of dreaming of applying her discoveries to people. In March 2014, pioneering American biologist and technologist Craig Venter
– along with the tech entrepreneur founder of the X Prize Foundation, Peter Diamandis – announced a new company called Human Longevity Inc.
It isn’t aimed at developing anti-ageing drugs or competing with Calico, says Venter. But it plans to create a giant database of 1 million human genome sequences by 2020, including from supercentenarians.
In an office not far from Google’s headquarters in Mountain View, with a beard reaching almost to his navel, Aubrey de Grey is enjoying the new buzz about defeating ageing.
[link to www.theguardian.com (secure)]

(April 4, 2015) Tech titans’ latest project: Defy death
Seated at the head of a table for 12 with a view of the city's soaring skyline, Peter Thiel
was deep in conversation with his guests, eclectic scientists whose research was considered radical, even heretical.
Among the guests was Cynthia Kenyon, a molecular biologist and biogerontologist who had garnered attention for doubling the life span
of a roundworm by disabling a single gene. Aubrey de Grey, a British computer scientist turned theoretician who prophesied that medical advances would stop aging.
And Larry Page, co-founder of an Internet search darling called Google that had big ideas to improve health through the terabytes of data it was collecting.
He and the tech titans who founded Google, Facebook, eBay, Napster and Netscape are using their billions to rewrite the nation’s science agenda and transform biomedical research.
The work they are funding includes hunting for the secrets of living organisms with insanely long lives, engineering microscopic nanobots that can fix your body from the inside out,
figuring out how to reprogram the DNA you were born with, and exploring ways to digitize your brain based on the theory that your mind could live long after your body expires.
“I believe that evolution is a true account of nature,” as Thiel put it. “But I think we should try to escape it or transcend it in our society.”
[link to www.washingtonpost.com (secure)]

(April 4, 2015) Another Personal Genetics Company Is Sharing Client Data
Today, personal genetics company AncestryDNA announced a partnership with the Google-owned biotech Calico,
which is working to research the biological drivers of longevity.
This collaboration is one of a few recent partnerships between personal genetics companies and pharma-minded businesses.
In January, the beleaguered 23andMe announced that it would share anonymized data on 650,000 of its customers with Pfizer,
as well as sequence the full genomes of 3,000 people with Parkinson's in a bid to develop a drug with Genentech.
Typically, it takes a lot of cajoling to get people—the research community would call them participants, or volunteers, or patients—
to part ways with their biological bits. But companies like AncestryDNA have convinced customers to pay to give their genetic data away,
at a cost of about $100 per sample. This is the same sort of bargain you make when you begrudgingly hand your personal information over to Google or Facebook:
You sacrifice some amount of data about yourself in return for added convenience.
While a consumer gets a certain amount of information from their genetic test—information about their ancestry,
or living relatives who have also gotten sequenced—their genetic data is almost always more valuable in aggregate.
And for Calico, a huge genetic database could be worth a lot, especially once data-miners combine it with Ancestry's forest of family trees.
[link to www.wired.com (secure)]

(January 11, 2017) Illumina wants to sequence your whole genome for $100
The first sequencing of the whole human genome in 2003 cost roughly $2.7 billion, but DNA sequencing giant Illumina has now unveiled a new machine
that the company says is “expected one day” to order up your whole genome for less than $100.
Illumina’s CEO Francis deSouza showed off the machine, called the NovaSeq, onstage at the JP Morgan Healthcare Conference
in downtown San Francisco today, telling the crowd the machine’s scanning speed could decipher an entire human genome in less than an hour.
Six customers have already come on board to test NovaSeq, including the Chan Zuckerberg Biohub (the life sciences arm started by Mark Zuckerberg and his wife Priscilla Chan),
the Broad Institute of MIT and Harvard and biotech companies Regeneron and Human Longevity Inc.
[link to techcrunch.com (secure)]

(March 6, 2018) What if billionaires could live forever?
Several billionaires, most of them Californians, have been funding firms involved in developing life-extension technologies.
What if they succeed? What if billionaires alive today live indefinitely and get ever richer?
Diamandis and Hariri's new venture is the latest example of a well-established phenomenon in Silicon Valley:
Extremely wealthy techno-optimists have for years been funding biomedical R&D companies meant to achieve immortality for their funders.
Some of the more recognizable names who have been putting money into such efforts: Larry Ellison (founder of Oracle),
Larry Page and Sergey Brin (founders of Google), Jeff Bezos (founder of Amazon), and Peter Thiel, cofounder of PayPal and Palantir Technologies.
Palantir, by the way, is a "big-data" company that uses algorithms to scan huge datasets for patterns.
It does a lot of work for US government intelligence agencies. Thiel is a radical corporate libertarian, and Silicon Valley's best-known Donald Trump supporter.
In late February, Diamandis wrote to subscribers of his email bulletin: "I asked the smartest people I know for their tech predictions for the next 20 years (2018 – 2038).
What are the breakthroughs we can expect on our countdown to the Singularity?" One of the predictions he listed was that by 2030, "humanity will have achieved Longevity Escape Velocity for the wealthiest."
[link to www.dw.com (secure)]

(November 12, 2019) Meet the Startup: Chronomics’ epigenetics out of the lab
At Chronomics, we are defining the objective measures of health that go beyond blunt measures of biological age
and have the power to support the longevity space through provision of tractable measures of efficacy and impact.
The longevity sector is hugely important for the future of health globally and we are excited to be delivering the tools
to support the companies developing the therapeutics and interventions that will define the future of prevention.
[link to www.longevity.technology (secure)]

(April 10, 2019) Long-lived bats could hold secrets to mammal longevity
Biologists found four bat lineages that live at least four times longer
than similar-sized mammals and revealed new traits associated with bat longevity.
University of Maryland researchers analyzed an evolutionary tree reconstructed from the DNA
of a majority of known bat species and found four bat lineages that exhibit extreme longevity.
They also identified, for the first time, two life history features that predict extended life spans in bats.
Their work is described in a research paper, published in the April 10, 2019 issue of the journal Biology Letters, which concluded that horseshoe bats,
long-eared bats, the common vampire bat and at least one lineage of mouse-eared bats all live at least four times longer than other, similarly sized mammals.
This ability allows a vampire bat to conserve energy if it fails to obtain a blood meal.
Scientists have previously suggested that the ability to tolerate variations in body temperature may enable some mammals to fight infection
better than those without that ability. This happens to a limited extent in humans when the immune system attempts to kill a virus or bacterial infection
by raising body temperature and causing a fever.
"If we lived as long as bats, adjusted for size, we could live 240 years," Wilkinson said.
"Everybody wants to know how these animals can live so long. This kind of work can help us get to the answers."
[link to www.sciencedaily.com (secure)]

(April 13, 2020) Rutgers' saliva-based test nets FDA green light for COVID-19
Clinical genomics researchers at Rutgers University have received the FDA’s first emergency authorization
for a COVID-19 diagnostic test that uses easy-to-collect saliva samples instead of the more difficult deep nose swabs.
Developed in collaboration with Accurate Diagnostic Labs and utilizing Spectrum DNA’s spit collection and preservation kits,
vthe researchers were able to show their saliva-based test performed just as well as as the potentially painful swabs
when searching for the specific RNA sequences linked to the novel coronavirus.
Built off a previously authorized COVID-19 test developed by Thermo Fisher,
Rutgers’ assay uses the same PCR hardware and chemical components as the company’s TaqPath kit.
Saliva specimens must be stored or transported at ambient temperatures, and tested within 48 hours of collection, according to the researchers.
[link to www.fiercebiotech.com (secure)]

(May 8, 2020) F.D.A. Clears First Home Saliva Test for Coronavirus
The Food and Drug Administration said on Friday that it had granted emergency authorization for the first at-home saliva collection kit
to test for the coronavirus. The test kit was developed by a Rutgers University laboratory, called RUCDR Infinite Biologics, in partnership with Spectrum Solutions and Accurate Diagnostic Labs.
“A patient can open the kit, spit into the tube, put the cap back on and ship it back to our lab,” said Dr. Andrew Brooks, chief operating officer and director of technology development at RUCDR.
“We bring the test to the patient, instead of the patient to the test.”
[link to www.nytimes.com (secure)]

(May 15, 2020) LabCorp launches return-to-work services for employers
LabCorp Employer Services provides customized return-to-work solutions
using LabCorp’s trained medical staff for employee check-in health questionnaires, temperature screens, and COVID-19 test collection
at the employer site or offsite. The service gives employers access to LabCorp’s COVID-19 testing solutions including its at-home collection test kit,
its fingerstick antibody blood test, and in the fall, flu vaccination services.
[link to www.mlo-online.com (secure)]

(May 20, 2020) Bill Maris, who started Google’s VC arm, brings on Google walkout organizer at his new venture firm
Section 32 is one of the newer bio investment funds on the block. It was founded by the first CEO of Google Ventures, Bill Maris,
who also helped start Calico, a Google project (now Alphabet company) dedicated to anti-aging technology.
So far, Section 32 has invested in about 40 companies, including Auris, a microsurgical robotics company that sold to Johnson & Johnson;
Alector, a therapeutics company focused on neurodegenerative diseases; and Vir, an infectious disease-focused company that is working on new vaccines,
including for Covid19. More broadly, the fund is also looking at machine learning, cybersecurity, oncology, infectious diseases, diagnostics and brain health.
Maris also remains interested in anti-aging technology, and he typically meets with three to five founders a week in the space. He doesn’t believe that Calico,
which he helped start, has done enough yet to prevent new players from getting into the space.
[link to www.cnbc.com (secure)]

(June 7, 2020) New saliva test could deliver Covid-19 result within one hour
The tests work by people spitting into a tube and posting the sample to a lab
A new saliva test could help the government meet its target of working out whether someone has coronavirus within 24 hours.
The government is in talks with British company Chronomics about rolling out the test which would involve people who are suspected to have Covid-19 spitting into a tube and posting the sample to a lab. The company is aiming to produce test results within one hour
of the samples arriving at labs.
[link to inews.co.uk (secure)]
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(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)]
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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
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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)]
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(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)]
 Quoting: Anonymous Coward 77795952


(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)]
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If gangstalking isn't morally objectionable, then neither is this.
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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)]
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(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)]
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(August 24, 2020) QIAGEN to Launch Easy-to-Use Digital Test in the U.S. for Rapid Detection of SARS-CoV-2 Antibodies Following FDA Emergency Use Authorization
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)]
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(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)]
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(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.
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(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)]
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(October 15, 2020) Google & Oracle to Monitor Americans Who Get Warp Speed’s Covid-19 Vaccine for up to Two Years
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)]
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Thread: COVID-19 RELATED TIMELINE
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(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)]
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(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)]
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Re: Google, Calico, 23andMe, Genentech, Facebook, AncestryDNA, Illumina, RUCDR Infinite Biologics - immortality for wealthiest
Susan and Anne Wojcicki are sisters. Susan, 50, is the CEO of YouTube and has long worked for Google. Anne, 45, cofounded and serves as CEO of the genetic testing website 23andMe. Anne married Sergey Brin, Google cofounder...
There's. A. H0le. In. The. Sky.
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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)]
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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.
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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)]





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