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efta-efta02100786DOJ Data Set 10CorrespondenceEFTA Document EFTA02100786
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EFTA DisclosureText extracted via OCR from the original document. May contain errors from the scanning process.
To:
Joseph Thakuri.
Cc:
Rich Kahn
From:
Sent:
Mon 3/3/2014 5:28:18 PM
Subject: Re: Jeffrey Epstein
sure...I have passed along
On Mar 3, 2014, at 12:13 PM, Joseph Thakuria
wrote:
Thanks, if you could also pass on to Jeffrey: The Y PO folks arc also awaiting this
NIGH IRB approval along with him for work beyond the DNA extraction. They
will nccd to get rc-consented and may even nccd to resubmit samples under the
new protocol. Assuming it goes through, they will have their exomes sequenced
while Jeffrey will have his full genome sequenced.
Joe Thakuria
On Sun, Mar 2, 2014 at 10:53 AM,
Hi Joe...I have passed along to JetTrey..thanks!
On Mar 1, 2014, at 2:41 PM, Joseph Thakuria
wrote:
wrote:
Hi Richard, my study is still awaiting irb approval at mgh.
Once that goes through, there'll be a consent form for Jeffrey
to review and sign and then I can forward the invoice from
Illumina for the rapid turn-around-time whole genome.
Once we have his data and go through the analyses Illumina
provides, I can discuss with him any extra value from using
additional tools for analyses.
The irb approval process will take 3-5 weeks in the best case
scenario. As a physician, I could just order it for him from
Illumina but Jeffrey and I agreed the research route made the
most sense. For one, ordering a whole genome on a
(presumably) healthy patient is not currently indicated. Doing
this as a patient (at least at mgh) would also entail creating a
medical record of the encounter and the results. Our plan is to
keep this data private - at least until he's had a chance to
review with me. So, for this reason, we also agreed to go the
"research study" route with his genome.
I've discussed doing Jeffrey's genome through my mgh study
with george church and he's fine with it. I'll coordinate getting
JE's samples from the pgp and moving all of it, or a portion
EFTA_R1_00708486
EFTA02100786
(aliquots of the dna and cell lines) to the new study (again,
after the mgh study is formally approved - that's the
bottleneck now).
with Jeffrey not on the cc, please pass the info above
on to him. Let me know if he has any questions. I can clarify
anything by email or phone.
Maybe there was a misunderstanding when I mentioned the
'rapid turnaround time' offering from illumina? This just means
illumina's role - the sequencing of the sample - is expedited.
There is no way, unfortunately, to expedite the MGH IRB
process for approving human research studies. (A lot of us
wish there was!)
Joe Thakuria
Jose.h V. Thakuria MD, MMSc
E FTA_R 1_00708487
EFTA02100787
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