Home DNA Sequencing 190
An anonymous reader writes "Wired is running an article about high-tech gifts for Christmas, including a home DNA sequencing kit targeted at kids for under $100. What's next, the Fisher Price Cloning kit?"
If you think the system is working, ask someone who's waiting for a prompt.
For Free? (Score:5, Informative)
Re:Wow (Score:4, Informative)
Re:Modding the Airzooka (Score:5, Informative)
Re:Anyone know how well it actually works? (Score:4, Informative)
Cyber Green? I think that's fairly safe.... Ethidium Bromide would be bad!
Would have been nice if they could have included some cheap and robust restriction enzyme, to produce fingerprints. However this would then require hybridisation with a probe to bring out a few bands - way too complex/expensive. Anyone think of a cheaper and easier way of producing a nice fingerprint? It would be good to have a Mark II kit that actually did something usefull...
Re:Wow (Score:5, Informative)
Its not quite what it says on the story, its not DNA sequencing its just a DNA seperation kit using the bog standard ethanol prep [exploratorium.edu] which you can do with washing up liquid, salt and a bottle of (80%) Polish vodka. The electrophoresis [nexusresearchgroup.com] step is quite nice using a battery to provide the DC current. However the kit is nothing you could not make yourself (Most of Molecular biology is really quite low tech the main requirement is getting pure reagents to do it with)
Thats not to say its not a cool gift/toy, at the very least the Centrifuge, and Electrophoresis chamber could probably be reused by the budding geekling
here [discovery.com] is the link to the actual product.
Re:Wow (Score:5, Informative)
All it gets you is a pattern of sites that the enzymes cut at, not a sequence. Still, this is how a lot of DNA work (particularly forensics) is done, and it's awesome enough for me to want one (even though I have ready access to the real stuff).
It will tell you if you have DNA but not much else (Score:2, Informative)
It's not DNA sequencing (Score:5, Informative)
It's not sequencing, not even real DNA viewing! (Score:5, Informative)
Re:For Free? (Score:2, Informative)
It is NOT a gene sequencer!!! (Score:2, Informative)
a bit more advanced version (No DIY though) (Score:2, Informative)
www.iwoot.com
you can get a different but more professional dna in a tin kit
http://www.iwantoneofthose.com/ProductDetails.asp
its not DIY though, its a mail in DNA kit
Re:Wow (Score:3, Informative)
You also get to do electrophoresis and take pictures of your product, which is kinda cool. I can just see what's going throuh those kids minds right now....So, how similar are fido and the cat? What if I compare little sister's DNA to mine? Hey, you hold down the dog while I get some blood....oops....
Re:Anyone know how well it actually works? (Score:5, Informative)
Well, it's a fair question, and to some degree it's difficult to answer, because ... well, at this point, a lot of DNA sequence information is kind of like Bernoulli's law before airplanes, or the rules of Boolean algebra before computers. IOW, we know that there's a lot we can do with the information, but we haven't actually built the machines yet.
That being said, there's a lot of useful work going on with at least some DNA sequence information right now. Here (as a comp. bio. grad student) are the ones I can think of at the moment:
Re:Anyone know how well it actually works? (Score:4, Informative)
And I'm pretty sure it intercolates as well (it only interacts with dsDNA), so it's a potential mutagen. Not proven, but still not up for handing out to kids.
I was just showing that to a labmate, and we think that it could simply be hemotoxylin (sp? I never write it out..as in H&E). It's purple, and since the gel should be fairly devoid of protein, it should specifically stain DNA.
Re:A small nit. (Score:2, Informative)
No I'm a molecular biologist I mean 80% by volume (160 proof) anything much less won't precipitate the DNA. I'm in the UK and can buy 80% vodka from my local supermarket. (I plan to buy a bottle and use it when doing demos for the university open day .... granted I'll empty the bottle and use the lab ethanol, but the appearance that counts.)
A little Googling gives me a 160 proof spirit Polmos Polish Pure Spirit [uq.edu.au] (about half way down the page). Technically it may not be a vodka, in my travels I read the a vodka has to be between 80 and 110 by proof (OTOH my brain cells will probably not make the distinction:-). I also came across references that booze above 140 proof was illegal to sell in the US
Re:It's not sequencing, not even real DNA viewing! (Score:3, Informative)
It does appear to be 'simulated' which is unfortunate but understandable. DNA stain is extremely carcinogenic. Since it must bind to DNA to work, there's no way to avoid that.
Of course, they could do a better job of making it clear that the results are simulated.
Re:Anyone know how well it actually works? (Score:5, Informative)
1. Obtain a pure sample of DNA to sequence. You have to know a little bit of the sequence at the start (not a problem - when you sequence an unknown DNA sample you usually chop it up into bite-sized chunks and insert them into bits of bacterial DNA to make lots of copies of them - this means the unknown DNA has bacterial DNA on either end of it and you already know the sequence of that part).
2. Make a short strand of DNA that binds to the known portion of DNA sequence at the start of unknown portion. These are called primers.
3. Mix the DNA to be sequenced with the primers, heat them up and cool them. This results in long pieces of uknown DNA with the primers stuck to the beginning.
4. Throw in the building blocks of DNA - but a small portion of them are essentially defective and marked with fluorescent tags.
5. Throw in DNA replicating enzymes - these guys look for primers and try to copy the unknown DNA starting at the side of the DNA with the primers attached.
The DNA replicating enzymes will copy the DNA until they accidentally grab a building-block which is defective (which happens a small portion of the time - since most of the building blocks in the mixture work fine). At that point the defective building block is attached to the end of the DNA strand and that strand cannot be copied further.
At the end you end up with a mix of DNA strands that look like:
1. Only one step of the DNA ladder copied - because the first block grabbed was defective.
2. Only two steps copied - the second block was defective.
3. Three blocks copied.
N. The whole strand is copied.
Each of these DNA strands is one step longer than the strand before it. Each has a fluorescent tag at the end - since each ends with a defective block.
You then put this mix of partial strands onto a gel and apply an electrical current - the bigger strands move through the gel more slowly (they get stuck in the pores in the gel).
You end up with a gel with a long ladder-like series of bands - each band is a DNA strand one step longer than the band before it. Each is fluorescently tagged.
Now here is the magic - back when you put the defective building blocks in you actually used a mixture of four blocks (the four types of steps in DNA) each with a different color tag on it. So each band is a different color - corresponding to the color of the last step that was added to the chain. The pattern of colors corresponds to the sequence of the DNA.
I tried to simplify this explanation for those with only a basic understanding of biochemistry. There are various ways of doing DNA sequencing, and these days much of it is automated.
Oh - where the computers come in is this:
A gel like the one I described can only handle pieces of DNA up to about 400 steps long. That means that you can only sequence 400 bases at a time (a base is a step in the DNA ladder). A human being has 4 billion bases in their DNA.
The way you sequence the whole human genome is to chop it up into lots of 400 base units. You actually take lots of copies of the human genome and chop it into lots of random pieces. Then you sequence pieces until you're sequenced about 40 billion bases. Then you have a computer run through the sequences looking for overlaps. The computer will find lots of regions that are sequenced several times, and some regions that weren't sequenced at all. However, it will give you a pretty good sequence of the overall genome, and then some careful followup work can fill in the gaps (the followup work is less easily automated, so they try to get most of it using the random method).
Re:home DNA test kits: bring 'em on (Score:3, Informative)