Archive for the ‘Turn your head and cough’
Recommissioned
The Presidential Commission for the Study of Bioethical Issues is back and better than ever…we hope:
The commission’s wider scope will also force some tough choices in deciding priorities, says [George] Annas. “Doctors’ [involvement in] force-feeding prisoners at Guantanamo, doctors and torture, and international human-research rules are pressing issues of our day which demand our attention,” he says. Among the other issues he thinks the commission should juggle are new reproductive technologies, an overhaul of informed-consent procedures and — perhaps most immediate — fairer ways to apportion health care.
To that modest list I’d add achieving peace in the Middle East, ending world hunger, eliminating poverty, curing cancer, and repairing the global economy. I can think of two guys I’d appoint immediately…at least, I think they’re two different guys.
Why not just cut them open and count the rings?
The first big test for GINA? Really?
The DNA test does not reveal an age, but it can reveal whether the player is the son of his claimed parents. Players have been known to find families willing to lend a younger child’s birth certificate so that a player can appear younger.
Miguel Sano, a top prospect in the Dominican Republic, was given DNA tests and a bone-scan procedure to help confirm that he was 16, he said in a telephone interview from his hometown, San Pedro de Macoris.
The DNA tests were conducted on Sano and his parents to determine if he was their son, he said. Sano’s sister underwent the bone scan as well, to help confirm that she was his older sister, and not a younger sibling whose birth certificate was used to falsify Sano’s age.
“In the eyes of baseball, there’s a huge difference between 16 and 19 years old,” said an international scout for a major league team. “It’s night and day. This is a runaway train they’re trying to put a lasso around.”
As ever, youth is wasted on the young. Play them off, son.
On diddlysquat
A friend alerted me to this Atlantic Monthly podcast because of Craig Venter’s discussion of genomic testing, which manages both to recycle old platitudes and be self-aggrandizing…all in less than a minute! An equally brief but more powerful viewing experience from the same podcast is Reed Tuckson on the endless health care policy debates.
HIPAA, Shmipaa

…The book also reveals that, during spring training in 1999, team doctors revealed to owner George Steinbrenner that Torre had prostate cancer - even before informing the manager himself.
A doctor who gets it
Dr. Shalom Kalnicki, chairman of Radiation Oncology at the Montefiore-Einstein Cancer Center, says he tries to guide his patients, explaining the importance of peer-reviewed information to help them filter out less reliable advice. He also encourages them to call or e-mail him with questions as they “study their own case.”
“We need to help them sort through it, not discourage the use of information,” he said. “We have to acknowledge that patients do this research. It’s important that instead of fighting against it, that we join them and become their coaches in the process.”
It’s my duck in a box!
I have tried to keep my big fat pie-hole shut about the ongoing battle over regulation of personal genomics companies and instead ply you all (my seven readers!) with genomic fluff because 1) I selfishly want to save a lot of the corporate personal genomics stuff for my book; 2) plenty of other folks have weighed in; and 3) I keep waiting for the curtain to fall on this theater of the absurd. Apparently the latter is not going to happen anytime soon:
Ann Willey, director of the Office of Laboratory Policy for New York State, who is both a board-certified geneticist and a lawyer, spoke last week at CHI’s Beyond Genome conference in San Francisco. “I think of this genomic profiling paradigm…as really a star,” Willey said. “By the time we get done regulating it…we’re going to have to force it into a globe and shear off some of its sparkling and promising aspects.”
***
Willey said regulation of these companies could potentially fall into several different categories, including the practice of medicine, or a laboratory, or information management. “The jury is out, we haven’t decided what it is,” said Willey. “Once we make it a duck, it better quack like a duck. No matter what box we put it in, we put constraints on it… But we don’t want to leave them in no box, because we have no oversight.” Willey said her office regularly sends warning letters to laboratory testing facilities, from tests on human genes to microbial flora. “We’re not picking on this [genome analysis] industry. We really want to make this work.
“But I’m from the government and I can’t always help.”
Hoo wee! Really fills one with confidence, don’t it? I only wish I’d stuck around Beyond Genome long enough to see the show.
I work as an Assistant Professor in the Duke University Institute for Genome Sciences & Policy (although this site and its content are my own).
In 2007 I became the fourth subject in Harvard geneticist George Church's Personal Genome Project. As the PGP moves forward, I am chronicling the dawn of personal genomics, that is, people obtaining their genomic information for whatever reason(s) and figuring out what to do with it. I am interested in the relevant technologies and especially the attendant privacy and other ethical/legal/social issues.
This blog may also discuss some of my non-genome interests or, to paraphrase Dwight Yoakam, "Guitars, Cadillacs, hillbilly music, etc etc."
The header image comes from the Liz Lerman Dance Exchange's multimedia performance piece, "Ferocious Beauty: Genome."