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November 7, 2009 1:38 PM PST

My dad used to say technology is advancing so quickly that, by the time a product reaches market, it is already obsolete. Moreover, if you wait just a little longer, you can pay a lot less. The sequencing of the human genome takes the advancement of technology, and its fast reduction in cost, to an entirely new level.

Whole-genome sequencing could be affordable and accurate enough to perform on every newborn with a simple heel-prick blood test in a matter of years.

(Credit: Elizabeth Armstrong Moore/CNET)

The Human Genome Project, which officially completed the mind-boggling achievement of sequencing Jim Watson's genome in 2006, carried the equally mind-boggling price tag of $3 billion. If I may be so bold as to use that word thrice in one paragraph, even more mind-boggling is that a company called Complete Genomics has just sequenced three human genomes for $4,400 in materials, with an error rate of less than one base in 100,000.

DNA sequencing technology, which could help us detect genetic predispositions to illnesses, customize treatments accordingly, lead to the development of new energy sources, etc., is currently being used to either do long reads of hundreds of bases on genomes that have yet to be sequenced (see the news this week on the full sequencing of the domestic horse genome), or shorter reads that only align with a genome we have already sequenced (ours, for example).

In a paper published in the journal Science on Thursday, Complete Genomics shares the methods it used, which John Timmer at Ars Technica describes as "clever variants of well known molecular biology techniques to read massive amounts of DNA fragments that are, in total, about 65 bases long."

Moreover, Complete Genomics used more common--read more affordable--materials. For a detailed explanation of how this was done, check out the paper in Science, or Timmer's illustrated translation for Ars Technica.

Complete Genomics is not the lone warrior in this field. As CNET's Stephen Shankland reported in October, IBM Research has jumped into the game, and hopes to reduce the cost of genetic testing to as little as $100 per person. And then there's genomic technology manufacturer Illumina, and 454 Life Sciences. The list grows.

At this rate of advancement, it has been widely reported that the technology for whole-genome sequencing could be affordable and accurate enough to perform on every newborn with a simple heel-prick blood test in a matter of years. This makes a lot of people uneasy for several reasons, not the least of which is privacy.

"Bad things can be done with the genome," Dr. Jay Flatley of Illumina tells Times Online. "It could predict something about someone--and you could potentially hand information to their employer or their insurance company. People have to recognize that this horse is out of the barn, and that your genome probably can't be protected, because everywhere you go you leave your genome behind."

I have to wonder which is more unnerving to most people--that others will be able to access our genomic fingerprints, or that our bodies are able to be so accurately read at all. The secrets currently locked within us carry a certain mystique, and once unlocked could be put to uses that are possibly beyond our control. Whether this makes the human body more or less magical is debatable, but this much is not: The horse is out of the barn.

Originally posted at Health Tech
Elizabeth Armstrong Moore is a freelance journalist based in Portland, Ore. She has contributed to Wired magazine, The Christian Science Monitor, and public radio. Her semi-obscure hobbies include unicycling, slacklining, hula-hooping, scuba diving, billiards, Sudoku, Magic the Gathering, and classical piano. She is a member of the CNET Blog Network and is not an employee of CNET.
November 5, 2009 10:56 AM PST

You've probably heard of or even owned a computer that automatically turns off its hard drive when it senses shock or heavy vibrations. That is an example of sensitive human-machine intimacy. Another example I like is tilting the iPhone to use it as the driving bar for my racing games. Well, that nifty human-to-computer interaction is about to go to whole new level.

HP announced Thursday a new inertial-sensing technology that enables the development of digital micro-electro-mechanical systems (MEMS) accelerometers that are up to 1,000 times more sensitive than those in high-volume products currently available.

A MEMS accelerometer is a sensor that can be used to measure vibration, shock, or change in velocity. When implemented, this allows the device to "feel" the environment it is in.

According to HP, the new sensing technology--the result of HP's 25 years of nano-sensing research--includes multiple detectors as part of a complete sensor network and therefore is capable of real-time data collection, management evaluation, and analysis. This information enables users to make better, faster decisions, and take subsequent action to improve safety, security, and sustainability.

... Read more
Originally posted at Crave
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October 26, 2009 2:59 PM PDT

Warwick Warp BioLog equipment is already in use on construction sites, where workers have notoriously abraded prints.

(Credit: University of Warwick)

It's long been held that no two fingerprints are exactly alike, rendering the old-fashioned print more reliable than current DNA sampling, which has resulted in false positive identifications.

But what if a fingerprint is warped? When I volunteered to be a mentor recently, I had to get my prints taken, and the process was tedious and full of re-dos because, as I rotated each finger, I tended to slightly smudge the results. (I might have made a good criminal, but I was an annoyed--and inky--mentor.)

Now, the biggest problem with fingerprints--that a good one is hard to find--may have finally been solved, according to new research out of the University of Warwick in the UK.

Most fingerprint techniques identify a handful of features on a print and match the entire set of characteristics against each fingerprint in a database of templates--a laborious, often time-consuming endeavor. Researchers at the University of Warwick took a different approach.

Considering the entire pattern of a print, they would transform its topology into a standard coordinate, thus allowing the "unwarping" of any print distorted by such common real-world issues as smudging and uneven pressure. The clearer digital representation of the print is then mapped onto an "image space" of all other prints in a given database, so instead of comparing one print to every other print in that database, the overlaying of the print against the entire database finds a match, if there is one, in seconds, regardless of whether that database holds a million or a thousand prints.

The unwarping is so effective, it turns out, that it even compares the position of individual sweat pores (there are hundreds) on a print. Previously, the slightest distortion of a print rendered these densely-packed pores unreadable.

The technology has already won over the construction industry, with spinout company Warwick Warp installing its BioLog for security and staff management at six building sites. (Apparently construction workers often have abraded fingerprints due to the nature of their work.)

And the results have already impressed more than the construction industry. In the past week, the technology has been examined by two of the world's most respected technical fingerprint benchmarking tests; the UK's National Physical Laboratory ranked Warwick Warp's fingerprint technology best overall for accuracy, and the National Institute of Standards and Technology in the U.S. ranked it third.

The signature may soon be obsolete. Want to use your credit card, see personal medical files, buy beer when you look underage? Take off your glove, please.

October 26, 2009 6:59 AM PDT

The Department of Energy on Monday named the first winners of a program aimed at generating breakthroughs in clean-energy technologies.

The program, called Advanced Research Projects Agency-Energy (ARPA-E), began taking applications earlier this year for research ideas that reduce imports of foreign fuel, cut greenhouse gas emissions, and improve energy efficiency. Funding for the agency is part of the Obama administration's goal to improve the economic competitiveness of the U.S. by investing in energy technology.

The DOE is awarding $151 million in 37 grants to both academics and green-tech companies, most of which are start-ups. The ideas are meant to be high-risk and high-reward, with a number not expected to meet their goals.

Authority to create the agency, roughly modeled on the DARPA defense program that spawned the space race, happened in 2007 but it wasn't funded until earlier this year. ARPA-E now has authority to fund as much as $400 million in research. A second tranche of grant awardees is scheduled to be announced later this fall.

Energy Secretary Steven Chu.

(Credit: Martin LaMonica/CNET)

The naming of ARPA-E grants is being closed watched in the green-tech start-up community and among researchers. There were 3,600 concept papers submitted, followed by 300 full applications and ultimately 37 awardees.

One awardee is an effort at the Massachusetts Institute of Technology to make an all-liquid battery, which would make storage of storage of solar and wind power more cost effective.

Another is funding for a bioreactor developed by the University of Minnesota that proposes using two microorganisms to make a vehicle fuel. One bacteria would convert sunlight and carbon dioxide into a sugar, and another would convert the sugar into a fuel.

Two other efforts include developing enzymes that would more effectively capture carbon dioxide from power plants and a low-cost material for making LED lighting. The full list of awardees is at the ARPA-E site (click for PDF).

Energy Secretary Steven Chu is scheduled to speak at Google Monday morning in Google to make an announcement, after which Google CEO Eric Schmidt will speak with Chu. Through its philanthropic arm Google.org, Google has invested in a number of renewable energy companies. It has also developed Web-based energy monitoring software for consumers.

Originally posted at Green Tech
October 21, 2009 12:18 PM PDT

Levi Morran, a graduate student at the University of Oregon, had the pleasure of watching 50 generations of roundworms procreate and concluded that, as problematic as males are, sex with a mate is better than sex alone.

(Credit: University of Oregon)

Sex with oneself in the world of plants and animals is called, fittingly, "selfing." The offspring of selfing females share 100 percent of their mothers' genes, and they can go on to produce their own offspring.

The offspring of "outcrossing" (the sexy science term for mating) males and females, on the other hand, share 50 percent of each parent's genes. Some offspring, naturally, are males that cannot bear offspring.

Of the two systems, it turns out that outcrossing produces offspring whose more diverse genetic codes lead to greater chances for longer lives, lower susceptibility to genetic mutations, and better adaptability to changing environments, according to more than 100 mini-evolution experiments with nematode worms at the University of Oregon. Researchers are reporting their findings, among creatures that can reproduce via both selfing and outcrossing, online on Wednesday in advance of regular publication in the journal Nature.

While selfing females don't have to put up with "pesky males" to reproduce, a problem known as the evolutionary "cost" of males, and they can, in fact, populate twice as quickly when going it alone, the genetic benefits of outcrossing explain why the phenomenon exists at all, the researchers explained.

"Biologists going all the way back to Charles Darwin have been puzzled why sexual reproduction via outcrossing exists at all," said UO biology professor Patrick C. Phillips, who turned to two of his students in the UO Center for Ecology and Evolutionary Biology to help determine what good could possibly come of worms having partners.

Levi Morran and Michelle Parmenter conducted more than 100 mini evolutions for 50 generations, in which 60 populations of nematodes, also known as roundworms, were adapted to new environments, including to the presence of a bacterial pathogen that eats worms from the inside out, according to a statement.

Morran and Parmenter genetically engineered the worms, which normally practice a combination of both selfing and outcrossing, to reproduce just one or the other. Strictly selfing populations, they found, were far more susceptible to accumulating harmful mutations and unable to adapt to rapidly changing environments.

"The inability of selfing populations to adapt to changing environmental conditions helps to explain the observation that selfing populations are much more likely to go extinct than outcrossing populations," says Morran, a graduate student and lead author of the study.

While males are clearly problematic for several reasons, their evolutionarily benefits do outweigh their costs, Phillips concludes. Sound familiar, ladies?

Originally posted at Health Tech
Elizabeth Armstrong Moore is a freelance journalist based in Portland, Ore. She has contributed to Wired magazine, The Christian Science Monitor, and public radio. Her semi-obscure hobbies include unicycling, slacklining, hula-hooping, scuba diving, billiards, Sudoku, Magic the Gathering, and classical piano. She is a member of the CNET Blog Network and is not an employee of CNET.
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October 13, 2009 12:26 PM PDT

Can a $1 billion help save the environment? George Soros hopes so.

The billionaire financier and philanthropist plans to invest part of his wealth on clean tech to fight global warming. In a speech at the Project Syndicate editors' forum in Copenhagen, Denmark, on Saturday, Soros gave the keynote address announcing his new plans.

Soros said he will invest $1 billion in clean-energy technologies and will provide $100 million--$10 million each year for the next 10 years--for the new Climate Policy Initiative, a watchdog-type foundation to promote measures to combat climate change.

"Global warming is a political problem," Soros announced to the meeting of editors in Copenhagen, the same city where representatives from around the world will meet in December to try to hammer out a new climate agreement. "The science is beyond dispute," he added, "but how do we achieve the objectives we all know are necessary? That is a political problem."

The need for cleaner coal has been a critical issue for Soros, who has invested in so-called "clean coal" technologies. In April, he was part of a consortium that funded $50 million toward PowerSpan, a firm researching and developing methods for cleaner coal.

On another front, Soros announced last year that his investment fund would pour $25 million in funds toward Qteros, a company that can make cleaner ethanol from a single microbe.

Soros offered few details on where he plans to invest the $1 billion. But he said he will look for profitable opportunities, and also "insist that the investments make a real contribution to solving the problem of climate change."

Clean energy has been a key issue for Soros. The billionaire has given speeches and interviews promoting development of alternative energy as not just a necessary goal but one that could revive the global economy.

Of course, clean energy has become an increasingly popular sector all around. A recent report on venture capital funding found that more money is being invested in green tech than in software or biotech.

Born in Budapest in 1930, Soros survived both the Nazi and Communist occupations of Hungary. After fleeing to England where he studied economics, he eventually settled in the United States. Soros amassed his huge fortune as the chairman of Soros Fund Management. He was recently ranked by Forbes as the 15th richest American, with an estimated net worth of $13 billion.

Originally posted at Green Tech
Lance Whitney wears a few different technology hats--journalist, Web developer, and software trainer. He's a contributing editor for Microsoft TechNet Magazine and writes for other computer publications and Web sites. You can follow Lance on Twitter at @lancewhit. Lance is a member of the CNET Blog Network, and he is not an employee of CNET.
October 10, 2009 11:10 AM PDT

A 32-year-old nuclear physicist, part of the Large Hadron Collider project on the Swiss-French border, has been arrested by French police on suspicion of involvement with al-Qaeda.

According to The Independent, the arrest was made after anti-terrorist police had followed his movements for more than a year. Le Figaro newspaper suggested that the man's name had originally come to light in connection with the "Afghan network" of terrorist groups based in Europe.

Of Algerian origin, he was arrested together with his brother, who was not working on the Collider.

Sources told The Independent that the scientist was not thought to be threatening the Collider itself, but rather was helping terrorists choose nuclear targets for attack.

The French Ministry of the Interior told Le Figaro that, having seized the man's two computers, three hard disks, and several USB keys, it believed the threat was serious. A Ministry spokesman said, "Our investigation showed without doubt that there were targets in France and elsewhere and indicated that we have perhaps avoided the worst."

CERN reassured the Independent that the suspect was not working on any of the major elements of the Collider, nor did he have access to the tunnel in which the Big Bang experiment is to be carried out. The CERN representative added, "None of our research has potential for military application, and all our results are published openly in the public domain."

The Collider is due to for a restart in November. One can only hope it's a safe one.

Originally posted at Technically Incorrect
Chris Matyszczyk is an award-winning creative director who advises major corporations on content creation and marketing. He brings an irreverent, sarcastic, and sometimes ironic voice to the tech world. He is a member of the CNET Blog Network and is not an employee of CNET.
October 6, 2009 10:57 AM PDT

If you were brought up a Catholic, as a child, you were taught about the power of mysteries.

One mystery that I used to always find perplexing was how the face of Jesus Christ was superimposed on the Turin Shroud, a burial cloth that measures 14 feet, 4 inches by 3 feet, 7 inches.

Somehow, the face looked a little too much like the Jesus in all the religious pictures. It all seemed a little too perfect. And, as one grew up, one began to learn that nothing was quite that perfect. Not even priests.

Now an Italian scientist and his team claim to have debunked this mystery.

According to Reuters, an organic chemist from the University of Pavia called Luigi Garlaschelli has created a shroud replica and plans to reveal the results of his work at a conference on the paranormal (and, who knows, of the paranormal) later this week.

An artistic depiction of the Shroud.

(Credit: CC Buridan/Flickr)

In order not to cheat, Garlaschelli says he availed himself only of materials that were accessible in the Middle Ages, the period from which carbon dating by various laboratories suggested the shroud emanates.

He and his team used a pigment that contained a little skeptical acid to do the basic rubbing on a volunteer wearing a Jesus mask.

Then, in a process that seems to eerily resemble the production of faded clothing by teenagers, they heated the shroud in an oven and washed it. Finally, they added a few holes and stains for additional authenticity.

It all sounds suspiciously easy. Indeed, it all sounds as if someone wants to create a little anti-Catholic publicity. (The Church doesn't even claim that the Turin Shroud is genuine.) As with so much research these days, it is good to look to the source of funding to see who might be so very keen to bankroll a debunking.

Garlaschelli admits that he did take money from an Italian association of atheists and agnostics. However, he has offered his services to the Church too. "Money has no odor," was his somewhat-romantic quote to Reuters.

But something about this experiment does suggest a peculiar smell. The University of Pavia is one of the oldest in Europe. Don't the professors have something a little more interesting to do than trying to upset my mum and dad?

Originally posted at Technically Incorrect
Chris Matyszczyk is an award-winning creative director who advises major corporations on content creation and marketing. He brings an irreverent, sarcastic, and sometimes ironic voice to the tech world. He is a member of the CNET Blog Network and is not an employee of CNET.
October 6, 2009 7:54 AM PDT

The 2009 Nobel Prize in Physics has been awarded for "two revolutionary optical technologies."

Charles K. Kao, who discovered how to transmit light through fiber optics, and the team of Willard S. Boyle and George E. Smith, who designed the first digital-imaging sensor, split the Nobel Prize, announced by the Nobel Foundation on Tuesday.

Born in Shanghai, Charles K. Kao made a discovery in 1966 that would lead to today's fiber optics. A man ahead of this time, Kao calculated how it would be possible to transmit light over 100 kilometers (62 miles), compared to only 20 meters (65 feet) for the fiber cables available in the '60s. He discovered that by removing impurities and creating a more pure type of glass, the fiber could be made more efficient and absorb less of the light over great distances.

Kao's research stimulated other scientists to join the effort, leading to the first ultrapure fiber cable created in 1970.

Another breakthrough in technology was the invention of the first successful digital-imaging sensor, used today in everything from consumer cameras to surgical devices.

Working at Bell Labs in New Jersey in 1969, Willard S. Boyle and George E. Smith built the first CCD (Charge-Coupled Device). Using the photoelectric effect theorized by Albert Einstein, the sensor transforms light into electric signals. The team's major hurdle was determining how to gather and read out those signals into a large number of pixels in a short burst of time.

The first consumer camera with a CCD was designed in 1981, leading to a revolution in digital photography.

Willard S. Boyle, left, and George E. Smith of Bell Labs invented charged-coupled devices (CCDs). In this 1974 photo, they are demonstrating an experimental TV camera that contains a CCD substitute for the vacuum tube of a conventional TV camera.

Willard S. Boyle, left, and George E. Smith of Bell Labs invented charged-coupled devices (CCDs). In this 1974 photo, they are demonstrating an experimental TV camera that contains a CCD substitute for the vacuum tube of a conventional TV camera.

(Credit: Alcatel-Lucent/Bell Labs)

"When combined with the laser and the transistor, the invention of an efficient, low-loss optical fiber has made nearly instantaneous communication possible across the entire globe," said H. Frederick Dylla, director of the American Institute of Physics. "This mode of communication is essential for high-speed internet and forms the optical backbone of 21st century commerce. The CCD sensor has revolutionized technical, professional, and consumer photography in the last few decades. Taken together these inventions may have had a greater impact on humanity than any others in the last half century."

Kao will take home one half of the award prize of 10 million Swedish kronor ($1.4 million) with the team of Boyle and Smith splitting the other half. Awarded by the The Royal Swedish Academy of Sciences, Nobel prizes are given each year for achievements in science, literature, and economics.

October 5, 2009 5:27 PM PDT
This illustration shows a strand of DNA traveling through a nanopore. With IBM's approach, some layers periodically stop the DNA strand while another measures its properties to determine its genetic information.

This illustration shows a strand of DNA traveling through a nanopore. With IBM's approach, some layers periodically stop the DNA strand while another measures its properties to determine its genetic information.

(Credit: IBM)

It took 13 years for researchers to catalog all the information in a human genome the first time. Now IBM believes it can do better--somewhat perversely by equipping a newer genetic sequencing method with brakes.

Big Blue is among those who believe electronics technology can be applied to the task of sequencing a person's genes, thereby bringing genetic testing into the computing era and lowering its cost to something like $100 to $1,000.

IBM is working on prototype DNA-processing electronics that slurps strands of DNA through an extremely small hole called a nanopore, measuring the electrical properties of the chemicals as they go by to determine the genetic information. That technique is used beyond IBM, but what Big Blue researchers have been working on is a way to slow down, an essential step toward improving its precision, said Gustavo Stolovitzky, manager of the IBM Functional Genomics and Systems Biology Group.

IBM Chief Executive Sam Palmisano is scheduled to unveil the project and what the company calls its "DNA transistor" Tuesday in a talk, "IT Innovation in Healthcare," at the Cleveland Clinic, IBM said.

The ultimate goal for such research is affordable genetic sequencing. "It would allow DNA sequences to be more or less routine," Stolovitzky said, forecasting that the technology will arrive in five or ten years.

OK, but why should you care?

"It would enable the possibility of going to the doctor with some infection, and the doctor gets the sequence pretty much on spot of the bacteria affecting the patient or the virus is in the blood," Stolovitzky said.

Or another possibility: knowing patients' specific genotypes could mean doctors would know if they had a negative reaction to some drug. That could mean some drugs useful that today are banned could become useful to a subset of the population.

IBM isn't the only one working on this technology. In addition to various academic efforts, start-up 23andMe offers some genetic analysis today.

The genes of animals and plants are encoded in DNA with just four molecular-scale substances--adenine, thymine, guanine, and cytosine. Their particular order governs not only their the formation of humans and other organisms but also the day-to-day biochemistry that keeps us alive.

IBM's sequencing technique to transcribe this biochemical data has been under way for three years, and it's easier said than done. The company is in the process of creating a new prototype device updated to reflect what IBM learned from an earlier one that didn't work as hoped.

"Translocation control we should have in a year's time more or less," Stolovitzky said, referring to the ability to ease the DNA through the nanopore one pair at a time.

The distance scales alone make the work difficult. Each DNA base is about 5 or 6 angstroms away from its neighbor--about half a billionth of a meter. By comparison, a human hair is colossal, about a ten-thousandth of a meter in diameter. And the DNA strands slip through a nanopore that's 2 to 3 billionths of a meter wide.

One problem with the nanopore approach is that it's hard to distinguish the four substances, called bases, as they slip through the hole. The four bases have overlapping electrical properties, so the more time spent measuring each, the better the accuracy.

IBM's approach uses a flat device about 250 nanometers on a side. It has very thin alternating layers of metal and a material called a dielectric. The nanopore is bored through these layers using an electron beam from a tunneling electron microscope, Stolovitzky said.

On one side of the layer is the DNA, unzipped from its familiar double-helix configuration with two strands of matched bases into a single strand with single bases. The single-strand is important in part because the distance between each pair increases to between 5 and 6 angstroms, making them more manageable than the double strand with bases 3.4 angstroms apart, he said.

The strand is pulled through the nanopore by an electrical field that attracts the negatively charged strand. But in the nanopore, some layers are electrically switched on to fix the strand in place for a tick of an electronic clock while another layer makes its measurement, Stolovitzky said.

Even slowed down, the process is fast compared with humans toiling away with pipettes and polymerase chain reaction equipment in a lab. "We think 1 millisecond should be a reasonable time to measure (a base)," Stolovitzky said. In other words, it would take about a second to perform 1,000 measurements.

The human genome has about 3 billion base pairs, so that's still a lot of time to do a full analysis. But it's sill more complicated because the chromosomes that house the genetic data must be broken up into smaller strands for practical reasons.

But IBM Research is happy to pursue a number of projects that may not pay off immediately, including work touching on nanotechnology, computing, and biotechnology. Whether it'll all come to fruition remains to be seen, but one way or the other, it's likely you'll know your own genetic data within a matter of years.

Originally posted at Deep Tech
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