Science

I read a while ago something about using magnetic(?) beads to
concentrate the DNA and use PCR to amplify DNA. I think the key
finding was that they could go directly to PCR without removing the
beads. I read it over a year ago so I'm not even sure I'm remembering
this correctly.

On Sat, Nov 30, 2013 at 6:11 PM, Simon Rose
<excaliburorama@googlemail.com> wrote:
> Does anyone know a protocol for extracting cell-free DNA from human urine?
> If possible I would like to try to detect apoptosis bands by running the
> extracted DNA on a gel. I am not sure this is possible in our lab,though.
>
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Try  some of Greg Egan's short stories (can't remember which ones exactly). A lot of them are molecular biology- based.

On Tuesday, November 5, 2013 1:39:35 AM UTC, Biotech Ryan wrote:

Hi All,

Just wondering if there was any hardcore Biohacker sci fi that you've read and would recommend? I love most hard sci fi but I've been looking specifically for hard biohacker sci fi, any suggestions?

R

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no one would advocate for an early pregnancy test on the market that
can give a result 3 weeks earlier but comes with a 40% error rate. it
sounds like 23andMe did not adequately quantify their error rates or
prove their science according to FDA standards.

also, please don't misconstrue "genomic data" as automagically
factual. Sample prep and readout thresholds make a big difference,
amongst other sources of error. are they doing samples in triplicate?
are they doing 10 runs per gene fingerprint? are they just doing one?
what are their positive and negative controls and how often are they
run? I don't think anyone knows what their protocols are or how they
do QA/QC.

these are just growing pains of a new industry. it's not going to kill
23andMe, and I expect the consumer will benefit from this additional
scrutiny (though prices may increase).

jordan



> On Nov 28, 2013, at 7:44 PM, Cathal Garvey <cathalgarvey@cathalgarvey.me> wrote:
>
> Aye, that'd be my idea, too. It's abhorrent to suggest that people
> should be locked out of their own genomes, but it's irresponsible to
> suggest that someone should be allowed to tell *others* what their
> genetic fate is without any responsibility for the consequences.
>
> Data is not diagnosis; I can tell someone "you look pale, you might be
> anaemic", and that's not a diagnosis, it's merely data; particularly
> if suffixed with "you should see a doctor/qualified nutritionist". If I
> offer a service where people send me selfies and I tell them whether or
> not they *are* anaemic, then I (in a hypothetical scenario where I'm
> under their auspices) deserve the FDA's ire.
>
> On Thu, 28 Nov 2013 17:31:35 -0700
> "Daniel C." <dcrookston@gmail.com> wrote:
>
>>> On Thu, Nov 28, 2013 at 4:05 PM, Jeswin <phillyj101@gmail.com> wrote:
>>>
>>> I thought the whole hullabaloo was the fact they were interpreting
>>> the data. Sure, you need accurate sequence reads but don't you
>>> cross a certain regulatory line when you start interpreting the
>>> data? Doesn't it then become a medical device like a glucose meter?
>>> I think the FDA sees potential for misuse. Didn't they start to
>>> regulate smartphone app makers who started to venture into the
>>> medical device area?
>>
>>
>> That was my impression as well, though I didn't read the letters
>> myself. If 23andMe wants to give people their genetic data and let
>> them analyze it themselves, that would probably be fine. But if you
>> start telling people that they have genes that predispose them to a
>> certain disease, they may take action based on that and suddenly
>> 23andMe is providing a medical diagnosis.
>>
>> I saw the other thread where some people were upset that the FDA
>> would do such a thing, and while I am generally a fan of freedom of
>> information I can also see the argument against 23andMe giving people
>> this kind of information about themselves without the proper context
>> or responsibility.
>>
>> -Dan
>

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Aye, that'd be my idea, too. It's abhorrent to suggest that people
should be locked out of their own genomes, but it's irresponsible to
suggest that someone should be allowed to tell *others* what their
genetic fate is without any responsibility for the consequences.

Data is not diagnosis; I can tell someone "you look pale, you might be
anaemic", and that's not a diagnosis, it's merely data; particularly
if suffixed with "you should see a doctor/qualified nutritionist". If I
offer a service where people send me selfies and I tell them whether or
not they *are* anaemic, then I (in a hypothetical scenario where I'm
under their auspices) deserve the FDA's ire.

On Thu, 28 Nov 2013 17:31:35 -0700
"Daniel C." <dcrookston@gmail.com> wrote:

> On Thu, Nov 28, 2013 at 4:05 PM, Jeswin <phillyj101@gmail.com> wrote:
>
> > I thought the whole hullabaloo was the fact they were interpreting
> > the data. Sure, you need accurate sequence reads but don't you
> > cross a certain regulatory line when you start interpreting the
> > data? Doesn't it then become a medical device like a glucose meter?
> > I think the FDA sees potential for misuse. Didn't they start to
> > regulate smartphone app makers who started to venture into the
> > medical device area?
>
>
> That was my impression as well, though I didn't read the letters
> myself. If 23andMe wants to give people their genetic data and let
> them analyze it themselves, that would probably be fine. But if you
> start telling people that they have genes that predispose them to a
> certain disease, they may take action based on that and suddenly
> 23andMe is providing a medical diagnosis.
>
> I saw the other thread where some people were upset that the FDA
> would do such a thing, and while I am generally a fan of freedom of
> information I can also see the argument against 23andMe giving people
> this kind of information about themselves without the proper context
> or responsibility.
>
> -Dan
>

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On Wed, Nov 27, 2013 at 3:28 PM, Bryan Bishop <kanzure@gmail.com> wrote:
> They blasted this out a few minutes ago:
>
> """
> Dear 23andMe Customers,
>
> I wanted to reach out to you about the FDA letter that was sent to 23andMe
> last Friday.
>
> It is absolutely critical that our consumers get high quality genetic data
> that they can trust. We have worked extensively with our lab partner to make
> sure that the results we return are accurate. We stand behind the data that
> we return to customers - but we recognize that the FDA needs to be convinced
> of the quality of our data as well.
>

I thought the whole hullabaloo was the fact they were interpreting the
data. Sure, you need accurate sequence reads but don't you cross a
certain regulatory line when you start interpreting the data? Doesn't
it then become a medical device like a glucose meter? I think the FDA
sees potential for misuse. Didn't they start to regulate smartphone
app makers who started to venture into the medical device area?

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Preamble: I don't personally know whether the FDA is attacking 23andme
for offering genetic sequence data, or for the *interpretation* of that
data in medical terms. So I'm assuming the latter, because it's more
sane.

My own 2c is this: If you give someone the letters of their genome as a
service, that's something that *should not, should never be regulated
except to enforce company-provided guarantees of validity or quality*.

That is, if you offer to run a basic PCR and your customers don't have
a reasonable expectation of perfection, then there's no regulatory
issue except your handling of their biological data outside of the
test. If you sequence their whole genome and they only asked for their
cucumber-taste gene, you're overstepping the contract and breaking some
basic bioethics guidelines; it's a basic violation of privacy.

However, the moment you either make a promise of quality or validity,
you're into "false advertising" territory if you don't match the
promise; that's not the FDA's job, but regulation here is sound, to
help assure customers that the market is sane.

Also, the moment you offer *medically relevant interpretation* of that
sequence data, I would say that counts as something that needs to be
regulated as a medical service. Here, things get fuzzy; is inferring
eye colour or cucumber tasting a medical issue? I would say no.
However, 23andme offers far more medically relevant information, going
so far as to offer "unlockable" data that might affect your mindset or
lifestyle. *This should be regulated, oh hell yes*.

However, the mode of regulation is critical to me. Customers should be
entitled to avail of these services at their whim. If "regulation"
means "by doctor's prescription", that's a blatant violation of what
seems to me a basic human right; to know thyself, to have
inalienable ownership and mastery over your own body. Of course, the
existence of gene patents proves that the Western World does not
acknowledge this ownership of self anyway, so it's not something that
can be leveraged; it's a dream, an ideal.

Rather, regulation should be an enforcement of standards, same as for
doctors' diagnoses. If 23andme are diagnosing genetic conditions, they
need to be A) really good at it and B) telling customers how likely
they are to be wrong and C) telling them the actual odds that the
diagnosis is relevant.

A) means "our sequences are 99.99% correct".
B) means "The SNP we identified is 99% likely* to coassort with a
disease allele".
C) means "Having the disease allele is 75% likely* to result in
noticeable symptoms or disease, and coupled to A+B this means you have
a 74.24% chance of noticing or suffering a disease.

If they can't offer these guarantees and match them in practise, they
should be liable for malpractice.

However, my impression is that the FDA is moving towards a more awful
model, where 23andme cannot offer relevant information or
interpretation, and must instead limit themselves to raw sequence data
without *any* inference or markup. For information, you would need a
medical opinion. While that might save a few people from spurious
worries due to false positives or overestimating their odds of disease,
it's fundamentally unsound; it forces people to beg for knowledge about
themselves. It takes away your right to know thyself.

So, that's my primary concern; if you cannot know thyself, it is
fundamentally unjust and should be struck down, vetoed, blatantly
ignored, etc.
If it's merely an issue of sketchy medical diagnosis and not of
self-knowledge, I'm on board for regulation provided it doesn't prevent
you from getting your sequence data and interpreting it for yourself.

Frankly, the model where 23andme provide cheap SNP data and third
parties offer interpretation suits me just fine. I'd still never use
23andme, because they're assholes and may decide to patent me, as they
have done to other customers.

*ignore my abuse of percentages and probabilities, please

On Wed, 27 Nov 2013 20:08:21 -0800
Srihari Yamanoor <yamanoor@gmail.com> wrote:

> Joe,
>
> Let me ask you this question. How do you believe the FDA should
> classify the PGEs, and how should they regulate them?
>
> The way I see it, as I have been reading more and more, in fact,
> looking at the letter, 23andme is making some really tall claims.
> They are trying to run serious medicine business as if it was a
> social media company. It doesn't seem inconceivable that there will
> be people who have some history of cancer or another chronic disease
> in their family history to read too much into this and take drastic,
> unintended consequences. Competitors are prone to follow their path,
> and the FDA will be left with a mess to handle if they don't act.
>
> By the way, something not being discussed, once devices and drugs
> come into the FDA purview, federal preemption takes over and
> companies, especially startups can defend themselves from spurious
> lawsuits, such as the ones torts try out. By the way, torts are
> paying attention to 23andme's current predicament, and that could
> compound their problem especially with the word tricks they are
> trying to play around the word "diagnostic".
>
> In addition, the FDA clearly considers apps/software as "devices".
> They do wish to regulate them, and will do so in some form or other.
> What might come as a surprise to many - most devices, from blood
> glucose monitors to radiofrequency generators have software in them,
> and that software is regulated to the extent that a specification
> needs to be laid out, a plan needs to be developed and adhered with,
> and controls need to be in place, just like design controls would be,
> for any device. Software updates too, are controlled, and cannot be
> performed without FDA approval.
>
> And before anyone gets very angry, I would like to remind everyone of
> two things - one, medical device and diagnostics companies do
> software control routinely, like the customers of the organization I
> work for. We, and in many cases they, have dedicated software teams
> that work quite well under commercial as well as regulatory
> pressures. People who develop apps should not have any issues doing
> this.
>
> Secondly, the moment something goes wrong; either with an app, a hip
> implant or an electric cigarette or a gene test, people will
> immediately blame the "government". At which point, Congress, will
> call a hearing and blast the FDA. You cannot really blame them for
> being paranoid.
>
> I do agree, that the FDA has the potential to over-reach, and this is
> really in the hands of Congress. Instead of trying to succumb to
> lobbying or scoring political points, they need to balance patient
> safety against profits when it comes to the FDA. They have been quite
> lacking in this, as with most other areas.
>
> Sincerely,
>
> Srihari
>
>
> On Wed, Nov 27, 2013 at 7:45 PM, Joe Gorse <jhgorse@gmail.com> wrote:
>
> > Srihari,
> >
> > I am receiving your point loud and clear, that this is entirely
> > 23andMe's fault for not playing within the current regulations, and
> > as an engineer and entrepreneur I understand and agree with that
> > part of the assessment. I would probably not have approached things
> > as they did, but it is hard to say that without seeing the whole
> > story which has yet to be told.
> >
> > However, again, I must categorically disagree with the FDA's
> > arbitrary assessment of this technology as "diagnostic" in order to
> > pull rank on what amounts to a startup company. The criteria for
> > the decision is based on open-ended policy which can be applied to
> > anything, therefore the FDA is actively choosing to make this an
> > issue. This creates a chilling effect for the startup industry and
> > innovators like myself and many others who intend to enter the
> > personal device healthcare market.
> >
> > Imagine you are Apple and somebody writes a healthcare "diagnostic"
> > App for the unlocked Cydia store. The FDA sees this and orders
> > Apple to halt production and sales of iOS devices until they prove
> > safety and effectiveness of their devices with this App. This would
> > clearly be a dilitary and frivolous thing to do, and a death
> > sentence for any startup company in Apple's shoes.
> >
> > The leadership of the FDA is largely aware of these issues but
> > claim they lack the resources
> > <http://www.youtube.com/watch?v=Qr77hbPFhIg> and political climate,
> > as you mentioned earlier, to address this type of reform head on
> > (small business ~22:00).
> >
> > The FDA also needs scientists to speak out and work with them to
> > improve, which is why I am concerned when I hear such ardent
> > black-and-white responses surrounding the 23andMe case. The
> > WhiteHouse.gov petition is an appropriate forum for some of that
> > feedback.
> >
> > Cheers,
> > Joe
> >
> > P.S. Full disclosure, I am not a 23andMe customer nor fan nor
> > affiliate. I am more concerned with the idea of personal genomic
> > data coming to market successfully.
> >
> > On Wed, Nov 27, 2013 at 3:53 PM, Srihari Yamanoor
> > <yamanoor@gmail.com>wrote:
> >
> >> Joe,
> >>
> >> And you are missing my point. I am not opposed to 23andme selling
> >> any research tools they see fit and neither does the FDA. The only
> >> thing the FDA has done is made the discovery that they are indeed
> >> selling a diagnostic device as defined by the CFR. This brings
> >> them under their purview. This is not the first communication from
> >> the FDA to 23andme, so they could have and should have been better
> >> prepared.
> >>
> >> The FDA of the United States, as ill equipped as it is, because of
> >> a congress that succumbed to lobbying, is still at the very
> >> cutting edge of regulations that lead to two very key things -
> >> safe and effective devices, be they therapeutic or diagnostic.
> >> This agency is the one, global agencies, and now even the EU
> >> agencies are modeling themselves after; after having failed to
> >> succeed with any other regulatory pathway. Even in recent history,
> >> when Congressional lobbying led to poor oversight and fast
> >> approval of knee implants (you can read about it all in the news),
> >> it only ended up hurting patients, so I am very suspicious of the
> >> need to suspend oversight, especially given how many customers I
> >> have seen regularly prepare for, and get approvals.
> >>
> >> The notion that the FDA is modeling all of its activities after the
> >> pharmaceutical industry is summarily mythical, as the codes, the
> >> enforcement pathways and pretty much everything is quite divergent.
> >>
> >
> > This is a bit of a straw man. Most, but definitely not "all" FDA,
> > pathways are modelled as a result of a natural evolutionary
> > cause-and-effect of serving pharmaceutical companies in the
> > majority of the submissions for approval. The FDA is aware of this
> > issue and has openly admitted it as of 2011. They have made good
> > progress along these lines, but again it can always be improved.
> >
> > The FDA is, effectively, a litigious shield for pharmaceutical
> > companies. Prior to any significant tort reform, this is an
> > essential function for big pharma to operate under any
> > circumstances. To this end the FDA has primarily adapted itself to
> > serve us in this fashion.
> >
> > Just in case my tone was not neutral before, I would like to be
> > clear that there is no value judgement from me one way or the other
> > on this point. This just how it is and how it came to be. The
> > information is to be used as a baseline for further action,
> > including how best to interface with the FDA (through a
> > pharmaceutical company or other known successful pathways) and
> > improvement for the future.
> >
> > I also believe that it is a bit excessive to deem 23andme as having
> > a
> >> solution that is far superior and unknown. When I was in graduate
> >> school, well before the company existed, Professors, CEOs and
> >> Researchers from everywhere came and talked about personalized
> >> medicine, diagnostic tools based on genes and such. Heck, that was
> >> so well personified by the "trichorder". The company may have
> >> executed and come up with a solution that now allows for a new
> >> market to be created, no one doubts that. But essentially they are
> >> in the body-fixing business, which is not new and not new for the
> >> FDA either. They may not have the "best" scientists and engineers
> >> out there, but they have pretty good ones.
> >>
> >
> > "Body-fixing business" in the same way that LoseIt! works as an App
> > for tracking calories on a smart phone or that supplements work from
> > bodybuilding.com. The distinction is not yet clearly defined. Until
> > a clear criteria can be used to actually technically describe the
> > scope in a meaningful way, it might as well just be considered the
> > roulette that it is.
> >
> > It would also serve them well to play nice with the FDA, as their
> > latest
> >> email suggests and create a path with perhaps lesser resistance
> >> for other companies. It is commonly known in the device industry
> >> that the "first-in-class" company always falls on the sword in one
> >> way or another.
> >>
> >> And for all this hand-wringing and fan-clubbing, 23andme has the
> >> money and means to fix something, for which only they are to blame.
> >>
> >> Sincerely,
> >>
> >> Srihari
> >>
> >>
> >> On Wed, Nov 27, 2013 at 12:20 PM, Joe Gorse <jhgorse@gmail.com>
> >> wrote:
> >>
> >>> Srihari and Matthew,
> >>>
> >>> Both of you are kind of missing the point. This is not about
> >>> direct therapies which have the capability to cause harm (as have
> >>> been often straw-manned in the larger conversation about this
> >>> topic), but who has the right to screen your genetic information
> >>> at a level consistent with consumer market rates.
> >>>
> >>> The distinction between "diagnostic" and "research and education"
> >>> purposes is significant. Nobody conducts research starting with
> >>> expensive "diagnostics", not scientists and especially not
> >>> engineers. We start with broad and low-cost screening to find the
> >>> areas to focus on and go from there as a starting point. To
> >>> consider this service a direct diagnostic that would lead
> >>> straight into harmful therapy is fundamentally a stretch, to say
> >>> the least.
> >>>
> >>> I will reiterate my thesis from above, because this reinforces the
> >>> larger point of this issue: what is the cost to society of *not*
> >>> having this information available to the consumer at all, even if
> >>> it may be flawed to some tolerance? If all of this information is
> >>> known genetically about humans and mammals in the lab, why has
> >>> virtually none of that made its way to a consumer affordable
> >>> services which allow us to individually benefit from all that
> >>> research which has occurred since Watson and Crick regarding the
> >>> human genome?
> >>>
> >>> The FDA is not currently equipped to handle this situation.
> >>> Reform is obviously necessary for a multitude of reasons outside
> >>> the scope of this particular conversation. Ignoring the
> >>> weaknesses of the FDA will only cause things to get worse before
> >>> reform can happen. This is clearly an area in which the FDA has
> >>> room for improvement and there is a low barrier for doing it.
> >>> They don't need additional labs or funding, just a hard look at
> >>> their policy, the economics, and their mission to public.
> >>>
> >>> Cheers,
> >>> Joe Gorse
> >>>
> >>>
> >>> On Wed, Nov 27, 2013 at 2:22 PM, Srihari Yamanoor
> >>> <yamanoor@gmail.com>wrote:
> >>>
> >>>> Sorry my fault. Thanks for correcting me! Also, please note this
> >>>> article before considering signing the petition. Fans of 23andme
> >>>> might be doing more harm than good. Read it carefully, and read
> >>>> the last paragraph. There is also another discussion going on at
> >>>> the Society of Participatory Medicine listserv.
> >>>>
> >>>>
> >>>> http://www.fiercemedicaldevices.com/story/23andme-digs-fda-wants-test-market/2013-11-27
> >>>>
> >>>> Sincerely,
> >>>>
> >>>> Srihari
> >>>>
> >>>>
> >>>> On Wed, Nov 27, 2013 at 10:49 AM, Matthew Harbowy
> >>>> <hbergeronx@gmail.com
> >>>> > wrote:
> >>>>
> >>>>> Except for the part where Srihari calls the 23andme CEO a "he",
> >>>>> Srihari is dead right. They have admitted their guilt in not
> >>>>> answering the FDA in a timely manner, silence being something
> >>>>> that you just don't do if you want to retain your head on your
> >>>>> shoulders. It's that simple.
> >>>>>
> >>>>> I am certain the maker of elixir sulfanilamide was just trying
> >>>>> to make a more palatable cough syrup, to "do good" and "improve
> >>>>> human health" when they chose ethylene glycol as an excipient,
> >>>>> and the result was many dead children, and among the first
> >>>>> moves toward what has become the FDA. If you don't know the
> >>>>> phrase "elixir sulfanilamide", go educate yourself right away.
> >>>>> Science, not good intentions or a good sellable story, is the
> >>>>> basis of interaction with the FDA. Science requires disclosing
> >>>>> facts and evidence, not wishes.
> >>>>>
> >>>>> Matt
> >>>>>
> >>>>> On Wednesday, November 27, 2013, Srihari Yamanoor wrote:
> >>>>>
> >>>>>> It is not the FDA's job to produce the data to defend 23andme.
> >>>>>> It is the company's job. They knew this. They were not "taken
> >>>>>> aback" or suddenly violated. Their CEO, should have received
> >>>>>> training on what he can and cannot say about their products on
> >>>>>> an interview or on marketing materials. And then again, maybe
> >>>>>> he decided to over-step anyway.
> >>>>>>
> >>>>>> If you want to sell a diagnostic product, anything above a
> >>>>>> tongue depressor in the United States, you pretty much enter
> >>>>>> at least a Class IIa or Class IIb classification, and you go
> >>>>>> through the approval process. You can even call ahead and
> >>>>>> discuss strategy with the FDA if you so wish.
> >>>>>>
> >>>>>> Even now, that is all 23andme has to do. Sit down across the
> >>>>>> table from the FDA, convince them of the science as it stands
> >>>>>> and get the hold removed should their products be based on
> >>>>>> science as acceptable by today's standards. This process keeps
> >>>>>> a lot of people alive and healthy in the United States.
> >>>>>>
> >>>>>> These are the facts as they stand, and I am sure the White
> >>>>>> House will inform you thus as well.
> >>>>>>
> >>>>>> Sincerely,
> >>>>>>
> >>>>>> Srihari
> >>>>>>
> >>>>>>
> >>>>>> On Wed, Nov 27, 2013 at 8:46 AM, Joe Gorse <jhgorse@gmail.com>
> >>>>>> wrote:
> >>>>>>
> >>>>>> Srihari,
> >>>>>>
> >>>>>> If the FDA decides to produce a legitimate claim, I might be
> >>>>>> inclined to agree. Since all I have seen so far from the FDA
> >>>>>> is authority posturing and frivolous harm scenarios, all I can
> >>>>>> say is that they lack the data to make the claim that 23andMe
> >>>>>> should stop doing what they are doing. It appears that they
> >>>>>> have not clearly considered the harm which would be caused by
> >>>>>> doing nothing at all, which in this case is significantly
> >>>>>> greater than doing something which may not be completely
> >>>>>> accurate.
> >>>>>>
> >>>>>> From the standpoint of risk vs reward, what 23andMe is doing is
> >>>>>> valuable even if their data is lossy. In this case, the value
> >>>>>> of any data (vs no data) should be clearly seen as a positive
> >>>>>> force to engage individuals to take more responsibility for
> >>>>>> their person health care whereas no data at all leaves us at
> >>>>>> the mercy of the current health care system. People will take
> >>>>>> this information and ask themselves, "What can I do to be or
> >>>>>> become healthy?" So they will go to their primary care
> >>>>>> physicians and ask, "What does this mean?" This can hardly be
> >>>>>> considered negative as some articles have been claiming.
> >>>>>>
> >>>>>> For the down side of the false-positive, no physician in their
> >>>>>> right mind would make life-or-death therapeutic decisions
> >>>>>> based on a single genetic data point from 23andMe. Individuals
> >>>>>> are limited in their ability to act in drastic therapies
> >>>>>> without physicians so the worse case scenario for the lone
> >>>>>> individual is depression and incorrect supplements. Still in
> >>>>>> either case, the focus is on the individual's health and the
> >>>>>> outcomes are more than likely to be positive once it becomes a
> >>>>>> goal to be healthy.
> >>>>>>
> >>>>>> The false-negative case is immaterial due to the fact that it
> >>>>>> leaves us in the same boat as we were before: at the mercy of
> >>>>>> the current healthcare system to detect, prevent, and repair
> >>>>>> us as needed. One could argue that it might give us a false
> >>>>>> confidence, though with placebo effect being relevant to
> >>>>>> medical interventions as well as this being a single point of
> >>>>>> data, I doubt a diabetic or cancer or Alzheimer patients will
> >>>>>> take a false-negative from 23andMe and say, "Well maybe I am
> >>>>>> not sick after all, I am going to stop taking my medicine."
> >>>>>>
> >>>>>> We can hardly see any real negative in this scenario unless
> >>>>>> someone has something to lose (or unless you believe in the
> >>>>>> Angelina Jolie mastectomy
> >>>>>> hypothesis<http://venturebeat.com/2013/11/26/warning-letter-to-23andme-could-be-a-landmark-case-for-health-care/>:
> >>>>>> crazed 23andMe customers cause havoc in hospitals and demand
> >>>>>> elective surgery), such as the established authorities and
> >>>>>> providers and vendors may have if they refuse to reform. What
> >>>>>> is at stake here is more than just a small squabble about
> >>>>>> accuracy, this is the future of medicine taking shape. I,
> >>>>>> personally, want the FDA to do better. Their rules tend to be
> >>>>>> made for pharmaceutical companies, which are who they
> >>>>>> primarily do business with so it has been reasonably come to
> >>>>>> be this way, but that hamper startups and individual
> >>>>>> scientists from contributing significantly to human therapies
> >>>>>> which can be used in the US.
> >>>>>>
> >>>>>> The opportunity cost of not having more people engaged in
> >>>>>> productive research for human-relevant interventions is so
> >>>>>> great that it is becoming a moral imperative for our society
> >>>>>> as a whole. That is to say, the cost we incur by NOT testing
> >>>>>> more therapies for human interventions and disease rescue is
> >>>>>> greater than those saved by over-conservatively doing the same
> >>>>>> thing we have been doing before (and failing with) instead. If
> >>>>>> human life is indeed precious, then the sheer economic waste
> >>>>>> of inaction as those who succumb to disease pass on without
> >>>>>> altering the chances of survival for those who will suffer
> >>>>>> after them should be enough to convince even the most cool
> >>>>>> rational head that regulatory change is necessary and pressing.
> >>>>>>
> >>>>>> So far, this 23andMe seems to be a case of regulation impeding
> >>>>>> instead of serving the interests of progress. Therefore the
> >>>>>> petition has my vote of confidence.
> >>>>>>
> >>>>>> Cheers,
> >>>>>> Joe Gorse
> >>>>>>
> >>>>>>
> >>>>>> On Wed, Nov 27, 2013 at 10:30 AM, Srihari Yamanoor <
> >>>>>> yamanoor@gmail.com> wrote:
> >>>>>>
> >>>>>> The best course for 23andme at this point is to tone down on
> >>>>>> their marketing claims, work with the FDA and seek appro
> >>>>>>
> >>>>>> To view this discussion on the web visit
> >>>>>> https://groups.google.com/d/msgid/diybio/CAGsdRYAk%3D1m2s1J9CQ%3DWdnHsSbWOSAdWoYBjed-CEAjqM1p6dQ%40mail.gmail.com
> >>>>>> .
> >>>>>> For more options, visit
> >>>>>> https://groups.google.com/groups/opt_out.
> >>>>>>
> >>>>> --
> >>>>> -- You received this message because you are subscribed to the
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> >>>>> visit this group at
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> >>>>> To view this discussion on the web visit
> >>>>> https://groups.google.com/d/msgid/diybio/CA%2BRBL9n0X2X_r%3Dd2aWihWopg3dpwrs2BNs9qHPEWruUDhpXrkg%40mail.gmail.com
> >>>>> .
> >>>>> For more options, visit
> >>>>> https://groups.google.com/groups/opt_out.
> >>>>>
> >>>>
> >>>>
> >>>>
> >>>> --
> >>>> Home: http://www.yamanoor.com/
> >>>>
> >>>> Photography: http://www.yamanoor.net/ and
> >>>> http://facebook.com/voxluma
> >>>>
> >>>> Laughs: http://ysrihari.blogspot.com/
> >>>>
> >>>> Medical Devices: http://chaaraka.blogspot.com/
> >>>>
> >>>> Earth: http://itshothere.org/
> >>>>
> >>>> --
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> >>>> .
> >>>>
> >>>> For more options, visit https://groups.google.com/groups/opt_out.
> >>>>
> >>>
> >>>
> >>>
> >>> --
> >>> Joe Gorse
> >>>
> >>> C: 440-552-0730
> >>> LI: Joe Gorse <http://www.linkedin.com/pub/joe-gorse/7/12/397>
> >>> FB: jhgiv <https://www.facebook.com/jhgiv>
> >>>
> >>> --
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> >>> .
> >>>
> >>> For more options, visit https://groups.google.com/groups/opt_out.
> >>>
> >>
> >>
> >>
> >> --
> >> Home: http://www.yamanoor.com/
> >>
> >> Photography: http://www.yamanoor.net/ and
> >> http://facebook.com/voxluma
> >>
> >> Laughs: http://ysrihari.blogspot.com/
> >>
> >> Medical Devices: http://chaaraka.blogspot.com/
> >>
> >> Earth: http://itshothere.org/
> >>
> >> --
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> >> https://groups.google.com/d/msgid/diybio/CAGsdRYDwbLNhT679ng183Do%2BasAieHhtHRcPM7Tut_SFqK75FA%40mail.gmail.com
> >> .
> >>
> >> For more options, visit https://groups.google.com/groups/opt_out.
> >>
> >
> >
> >
> > --
> > Joe Gorse
> >
> > C: 440-552-0730
> > LI: Joe Gorse <http://www.linkedin.com/pub/joe-gorse/7/12/397>
> > FB: jhgiv <https://www.facebook.com/jhgiv>
> >
> > --
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> > .
> > For more options, visit https://groups.google.com/groups/opt_out.
> >
>
>
>