And here's a nice feature on the really ambitious efforts, which conceive of genome sequencing for $100, never mind $1000
http://www.technolog.../Biotech/20640/
Posted 17 April 2008 - 04:05 AM
Posted 17 April 2008 - 04:25 AM
Posted 24 February 2009 - 10:00 PM
Posted 15 March 2009 - 11:26 PM
Posted 12 June 2009 - 04:17 AM
Posted 12 June 2009 - 11:21 PM
While $48,000 is still out of reach for most consumers, the price reflects an exponential drop in the cost of sequencing technologies in recent years. James Watson's genome, sequenced in 2007, cost about $2 million, and Knome initially offered its service at $350,000. A third company, Complete Genomics, announced plans for a $5,000 sequencing service, although this will initially be available only to academic institutions and industry for research and clinical trials rather than for personal use. "It's like watching the price of gas fall," says George Church, a genomics technologist at Harvard University who has developed his own sequencing technology.
Posted 13 June 2009 - 10:40 PM
Posted 14 June 2009 - 11:00 PM
Edited by athrahasis, 14 June 2009 - 11:02 PM.
Posted 26 June 2009 - 11:10 PM
It's dropping at a remarkable rate. If it's $1,000 in 3 or 4 years, I'm getting this done.
Posted 26 June 2009 - 11:48 PM
Edited by forever freedom, 26 June 2009 - 11:49 PM.
Posted 27 June 2009 - 02:26 AM
Posted 27 June 2009 - 03:46 AM
Posted 27 June 2009 - 05:07 AM
What would you get from a full genome that you wouldn't get from a catalog of all known SNPs? I guess there would be a few things that might show up, like gene duplications and other large-order weirdness, but would we know what any of that meant? It seems like with a cheap SNP scan, at worst you would need to re-scan after a few years if/when critical new SNPs were discovered.
Posted 28 July 2009 - 05:00 AM
Posted 22 September 2009 - 11:55 AM
Leading third-generation sequencing company Pacific Biosciences affirmed at the Cold Springs Harbor Laboratory Personal Genomes meeting September 14-17, 2009 that the company has 12 prototype instruments in operation and continues to be on track for ~$100 (“the cost of a nice dinner”) whole human genome sequencing to be commercially available in the second half of 2010. NimbleGen indicated that they may have a $2,000 exome sequencer available in 2010.
Posted 22 September 2009 - 05:15 PM
Posted 01 October 2009 - 05:18 PM
Posted 08 November 2009 - 02:37 PM
Posted 08 November 2009 - 04:45 PM
Edited by forever freedom, 08 November 2009 - 04:45 PM.
Posted 09 November 2009 - 02:03 AM
Posted 09 November 2009 - 05:11 AM
Close as in "order of magnitude" close? Yep. Bait and switch prizes do not count. Companies could give away whole genome sequencing for free if they wanted, but what counts is whether someone can sell it and make money (otherwise it's not becoming mainstream).
Posted 09 November 2009 - 05:45 AM
Posted 09 November 2009 - 06:02 AM
Posted 10 November 2009 - 05:52 AM
Posted 16 November 2009 - 04:30 PM
The cost of full genome sequencing has dropped yet again, according to the latest announcements by Complete Genomics:
http://www.technolog...ne/23891/page1/
Hey, so we're finally there - the day of affordable sequencing has arrived.
So when will these services really become widely available to the masses?
How long until they tangibly impact our day-to-day healthcare, and our visits to the doctor's office?
Who here is planning to get their genome fully sequenced? Anyone against doing it?
, a start-up based in Mountain View, CA, has again lowered the stick in the financial limbo dance of human genome sequencing, announcing in the journal Science that it has sequenced three human genomes for an average cost of $4,400.Complete Genomics
Posted 18 November 2009 - 02:33 PM
Posted 22 November 2009 - 07:29 AM
Posted 22 December 2009 - 01:33 PM
Boston University biomedical engineers have devised a method for making future genome sequencing faster and cheaper by dramatically reducing the amount of DNA required, thus eliminating the expensive, time-consuming and error-prone step of DNA amplification.
Posted 04 January 2010 - 06:00 PM
Traditional methods for reading the genetic script, made up of four nucleotide bases, adenine, thymine, cytosine and guanine (labeled A,T,C,&G), typically rely on shredding the DNA molecule into hundreds of thousands of pieces, reading these abbreviated sections and finally, reconstructing the full genetic sequence with the aid of massive computing power. A decade ago, the first human genome—a sequence of over 3 billion chemical base pairs—was successfully decoded, in a biological tour de force. The undertaking required around 11 years of painstaking effort at a cost of $1 billion dollars. In addition to the laboriousness of existing techniques, accuracy is compromised, with errors accumulating in proportion to the number of fragments to be read.
A new strategy involves the use of nanopores—orifices of molecular diameter that connect two fluid reservoirs. A constant voltage can be applied between two electrodes located at either end of the nanopore , inducing an ionic current to flow through the length of the nanopore's enclosed channel. At this scale, the passage of even a single molecule generates a detectable change in the flow of ionic current through the pore. This current is then electronically amplified and measured. Only fairly recently have state of the art micro-manufacturing techniques enabled researchers to construct nanopores at the scale of individual molecules, opening up many new possibilities for single-molecule manipulation and research.
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