I was shaking my head the whole time I was reading this article:
Over-the-counter DNA kit worries genetics experts...
It's really hard to explain just how complicated genetic testing is. I think an early assumption many people make is that you do the test to look for 'the gene' and it's either there or it isn't - simple! When the fact of the matter is we all have 'the gene' i.e. basically the same set of around 30,000 genes, and genetic testing searches for miniscule changes within genes (and even that's a simplification of the process!).
One single letter change amongst a million letter long piece of DNA is pretty easy to miss, yet one single letter change can have vast consequences (such as leading to an 100% lifetime risk of bowel cancer in the case of the genetic disease FAP). These over the counter DNA kits simply cannot test for everything. Not even close. There is a very real chance that the results people get back from these tests will be misinterpreted.
Friday, May 21, 2010
Pick up a genetic test at your local supermarket - too easy!
Posted at
12:32 AM
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Labels: genetic testing, risk perception
Monday, May 17, 2010
Love vs Genetics
http://www.jpost.com/Opinion/Op-EdContributors/Article.aspx?id=173921
(Would it) be better if people with disabilities, people such as Beethoven and Stephen Hawking, did not come into the world and that parents of the genetically disabled should never be married, for fear of producing a defective child?
...Certainly, the battle between our hearts and our intellect, love and convenience, is one as old as the Jewish people.
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12:23 AM
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Labels: genetic discrimination, pgd, preimplantation genetic diagnosis, prenatal diagnosis, risk perception
Friday, April 16, 2010
Buying brains
Buyers of "donor" eggs offer more money to women who are likely to yield smarter kids...
Levine analyzed more than 100 ads placed in 63 college newspapers to recruit egg donors. Of these ads, 21 specified a minimum requisite SAT score.
http://www.slate.com/id/2249098
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12:08 AM
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Tuesday, April 6, 2010
Eugenics in 2010
Creepy...
http://www.lifenews.com/bio3080.html
Posted at
9:20 PM
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Labels: eugenics, genetic discrimination, prenatal diagnosis
Rise in marriages between cousins ‘is putting children’s health at risk’
I'm not an 'arranged marriage' advocate, but I think this may be a little OTT, Lady D:
Lady Deech, who chaired the Human Fertilisation and Embryology Authority for eight years, will also suggest that married first cousins use in vitro fertilisation so that embryos can be tested for recessive diseases.See the UK Times Online article about Lady Deech's campaign to "deter the practice of marriage between first cousins" here: http://www.timesonline.co.uk/tol/news/uk/health/article7069255.ece
Talk about controversial. In my Grad Dip of Genetic Counselling, I was always taught that the idea that marrying your first cousin would produce a baby with three heads was a lot overrated. And that in fact consanguineous marriages only had a slightly increased chance of producing a baby with a birth defect over the general population i.e. 6% affected births as opposed to 3-4% in the general population. This is because many recessive genetic conditions are exceedingly rare in the first place. When you put it like that, 3-4 vs 6, it doesn't seem like much, does it? Just goes to show the power (and tyranny) of statistics in furthering (and ?twisting) an argument.
Afterthought: Risk perception is very subjective. Non-directive genetic counselling is practically difficult.
Posted at
8:27 PM
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Labels: ethics, genetic screening, pgd, preimplantation genetic diagnosis, risk perception
Can a bad mother help her nature?
The old chestnut (debate) about genes and the environment, and how much influence each has on shaping who we are... Could some behaviours be 'written' in your genes? Or is there always room for social intervention?
http://women.timesonline.co.uk/tol/life_and_style/women/families/article7076033.ece
“We believe that a certain number of these ‘maternal neurons’ need to be ‘switched on’ for good mothering to take place... ...Our research showed that the (rodent) mothers with fewer than this number of ‘maternal neurons’ tended to neglect or abuse their offspring, while those animals with the lowest numbers actually savaged or killed their own young.”Hmmm. Crazy world we are headed for.
Similar techniques could soon be used to identify human mothers with the capacity to abuse their children...
Posted at
7:37 PM
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Labels: determinism, genes and behaviour
Sunday, March 28, 2010
Our society will be worse off if we reject Down syndrome children: a view from the archdiocese
Article from the Sydney Morning Herald:
Our society will be worse off if we reject Down syndrome children
http://www.smh.com.au/opinion/society-and-culture/our-society-will-be-worse-off-if-we-reject-down-syndrome-children-20100328-r51x.html
Very interesting comments at the bottom of the article too, from people who disagree.
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5:14 PM
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Labels: ethics, eugenics, genetic screening, genetic testing, prenatal diagnosis
Monday, March 22, 2010
Eliminating Suffering or Eliminating People?
Below are a couple of articles which help us to explore a world where genetic knowledge is at our fingertips, and lives can be planned or avoided, as the case may be.
Eliminating Suffering or Eliminating People? article by Amy Julia Becker.
No parent wants a child to suffer. Screening tests at every level help humans to eliminate genetic disease and, therefore, human suffering. And yet Christians have good reason to be concerned about the use of these tests, and to advocate for the protection of human life, however it is given to us...
Maybe it's not just the Christians who should be 'concerned'. The use of preimplantation diagnosis (PGD), prenatal diagnosis (PND), and genetic screening, their feasibility and uptake, are increasing at a rapid rate. And with an ever-increasing array of genetic 'conditions' being selected against, what is the logical endpoint?
Reducing people to a medical diagnosis, and the devaluation of disability and illness are themes in a well-written article 'The Gene Genie' by Kathy Evans in The Age, 14 March 2010.
''Given the cost of raising a child with a serious genetic disease - that's a massive cost to the community over many, many years - PGD is very economical. We do not make a profit out of it; we do it because we believe it is a worthwhile service... You have to take into account a family's personal circumstances and the impact of the disease on the family,'' Wilton says.
It's a bit sad when lives get drilled down to dollars and cents. But maybe naive to believe society won't operate like that. And for families who have been terribly affected by a genetic condition, who can blame them for wanting to prevent their children (and themselves) from more suffering?
Afterthought: And reducing variation runs counter to natural evolution. Nothing religious or superstitious about that.
Posted at
7:03 PM
2
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Labels: eugenics, genetic screening, pgd, pnd, preimplantation genetic diagnosis, prenatal diagnosis
Thursday, March 18, 2010
Keep every American's DNA profile on file
What's the difference between DNA sequencing and DNA profiling? In this article Yale Law student, Michael Seringhaus, explains:
A DNA profile distills a person's complex genomic information down to a set of 26 numerical values, each characterizing the length of a certain repeated sequence of "junk" DNA that differs from person to person...Read the article here:
The genetic privacy risk from such profiling is virtually nil, because these records include none of the health and biological data present in one's genome as a whole. Aside from the ability in some cases to determine whether two individuals are closely related, DNA profiles have nothing sensitive to disclose.
http://www.dallasnews.com/sharedcontent/dws/dn/opinion/viewpoints/stories/DN-seringhaus_18edi.State.Edition1.27088d3.html
Posted at
11:20 PM
1 comments
Labels: genetic profile, privacy, sequencing
Tuesday, March 16, 2010
Biopirates!
Sensational stuff. Almost worth fighting for?
http://www.cpa.org.au/guardian/2010/1447/11-privatisation.html
Most of the genes... were acquired by theft, more commonly referred to as Biopiracy. Biopiracy involves the monopolisation by private corporations of genetic resources and traditional knowledge or culture taken from indigenous peoples and local communities...
Posted at
4:55 PM
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Labels: gene patenting, gene patents, law
Sunday, March 14, 2010
Genome sequencing: Would you do it if you could?
"Having your DNA fully sequenced is the genetic equivalent of space tourism"
It currently costs tens of thousands of dollars to have your genome sequenced, but costs are are coming down at a rapid rate. Pretty soon all of us will realistically be able consider having our genomes sequenced and possibly finding out a lot more about ourselves than we bargained for!
Will you succumb to curiosity, or are you concerned about possible privacy repercussions/current lack of legislation (at least in Australia) protecting this very personal information?
Read about how Glenn Close has made the leap in this article from the UK Times Online:
http://www.timesonline.co.uk/tol/news/science/genetics/article7060870.ece
If you are unfamiliar with the difference between genetic screening, genetic testing and gene sequencing and the associated ethical issues, read this article 'Genomics gets personal' for a bit of background.
Posted at
10:54 PM
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Labels: genetic testing, law, privacy, sequencing
Thursday, March 11, 2010
Genomics Law Report
US website:
News and analysis from the intersection of genomics, personalized medicine and the law
http://www.genomicslawreport.com/
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6:21 PM
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Tuesday, March 9, 2010
DNA deception
Edit: More recent article about the same issue 9 March 2010 http://www.texastribune.org/stories/2010/mar/09/blood-drive/
Article from the Texas Tribune 22 Feb 2010:
When they were sued last year for storing baby blood samples without parental consent, Texas health officials said they'd done it for medical research. They never said they turned over the blood spots to the federal government to help build a vast DNA database. A Texas Tribune review of nine years' worth of e-mails and internal documents on the Department of State Health Services’ newborn blood screening program, released after the state settled the case so quickly that it never reached the discovery phase, shows an effort to limit the public’s knowledge of the program.
http://www.texastribune.org/stories/2010/feb/22/dna-deception/
Posted at
5:29 PM
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Labels: ethics, genetic research, genetic testing, privacy
Tuesday, March 2, 2010
Cracking an ancient code
A Sydney scientist believes Africa can unlock the secrets of disease... Article from the Sydney Morning Herald:
http://www.smh.com.au/world/science/cracking-an-ancient-code-20100218-oedd.html
No need to sugar coat it by saying it's for the "benefit of indigenous people", but this is some interesting research anyway.
Posted at
10:17 PM
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Labels: genetic research, sequencing
Should cops be required to submit DNA samples?
Providing DNA samples as a condition of employment is not yet an issue in law enforcement, but we should contemplate the ramifications should that day arrive
http://www.policeone.com/csi-forensics/articles/2008924-Should-cops-be-required-to-submit-DNA-samples/
Very interesting article from the PoliceOne.com website
Posted at
9:02 PM
0
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Labels: ethics, genetic discrimination, genetic testing, privacy
Sunday, February 28, 2010
Ethics of Genetics
Ethics of Genetics Section on 'The Human Genome' website
http://genome.wellcome.ac.uk/node30069.html
Posted at
3:09 PM
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