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Quantum fluctuations in science, space and society, from quarks to Hubble and Mars. Served up by Alan Boyle, NBC News Digital science editor. E-mail Alan, or connect via Facebook, Twitter or Google+.

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  • 28
    Sep
    2011
    3:52pm, EDT

    Glowing bacteria encrypt codes

    Manuel A Palacios / Tufts University

    E. coli engineered to glow certain colors when excited by the right light can convey a top-secret message.

    By John Roach, Contributing Writer, NBC News

    Scientists are tweaking bacteria to send encrypted messages that can be shipped via snail mail on sheets of paper-like material called nitrocellulose.

    The recipient grows the bacteria with a select cocktail of nutrients and other chemicals. Once grown, each microbe glows one of seven colors when exposed to the right kind of light. Different colored microbes are arranged to represent different letters and symbols. If you know the nutrient and chemical cocktail as well as the keys to the code, you can decipher the message.


    For an added layer of security, many glowing microbes can be sent along, but only those that survive a dose of a particular antibiotic will reveal the intended message when exposed to the right light. 

    "There are several layers of encoding in the message," Manuel Palacios, a chemist at Tufts University in Medford, Mass., and lead author of a paper on the technique, told me today.

    To prove the point, the team created a message that when exposed to ampicillin read "this is a bioencoded message from the walt lab at tufts university 2011." The drug kanamycin gave different glowing bacteria that encoded the message: "you have used the wrong cipher and the message is gibberish."

    Palacios and his colleagues named this biological messaging steganography by printed arrays of microbes, or SPAM. They describe it in this week's issue of the Proceedings of the National Academy of Sciences. 

    The technology is rooted in funding from DARPA, the military's high-tech research agency, which suggests real-world spies could be communicating with messages encoded in arrays of glowing bugs. 

    "I love that this triggers all this discussion about spies and stuff," Palacios noted, but said practical applications are more likely to be found in the biotech world.

    For example, a biotech company that develops a high-yielding variety of genetically modified corn could use this technique to give the plant an easily-identifiable characteristic that thwarts attempts to steal it. 

    Currently, biotech companies stamp the genetic code of their modified crops, but genetic sequencing in the lab is required to read the stamp.

    "With this method, we are demonstrating that we can encode genetic information and we can decode it into something that just by looking at it you will be able to know what the message is," Palacios explained. 

    In this case, the message isn't top secret. Rather it is not obvious. So, for example, a corn stalk could be engineered to carry a biobarcode that can identify the plant as proprietary.

    "That's where we might be seeing an application in the future," Palacios said.

    More on secret messages:

    • Strange twists in a DNA message
    • Plants that glow on their own developed
    • Researchers store data in DNA bacteria
    • Spy trick hides message in plain sight

     


    John Roach is a contributing writer for msnbc.com.

     

     

     

    Sal Khan, a math whiz with an encouragingly at-ease lecture style, explains how his online education classes will be able to branch out into subjects beyond his expertise.

     

    3 comments

    If memory serves, isn't nitrocellulose highly combustible and even explosive? I believe it was once called "gun cotton" and was also the cause of many terrible fires involving old movie film.

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  • 29
    Jul
    2011
    1:36pm, EDT

    Test-tube brain aces 'plop' quiz

    Caltech

    Scientists have created an artifical neural network out of DNA, creating a circuit of interacting molecules.

    By John Roach, Contributing Writer, NBC News

    Artificial intelligence is no longer the domain of clunky, mechanical robots and computers. It thrives inside a test tube, where scientists have created an artificial neural network made out of DNA — essentially the beginnings of a brain — that was able to ace "plop" quizzes.

    The network is a circuit of interacting molecules that can recall memories based on incomplete patterns. It consists of four artificial neurons made from 112 distinct DNA strands and plays a mind-reading game in which it tries to identify a mystery scientist.


    The team, led by bioengineer Lulu Qian at the California Institute of Technology, chose to build its network out of DNA molecules because, before brains evolved, molecular interactions inside single-cell organisms showed limited forms of intelligence such as searching for food and avoiding toxins.

    "Molecules can act as biochemical circuits that process information and perform computational tasks," Qian explains in a video describing her team's work, which was published in the July 21 issue of Nature.

    Because scientists can synthesize DNA strands with whatever base sequence they want, the researchers were able to program the molecules to function like a simple model neuron that fires only when it passes a certain threshold. Linked together, they behave like a network of neurons.

    To play the plop quiz game, the neural network was trained to "know" four scientists, whose identities are each represented by a specific, unique set of answers to four yes or no questions, such as whether the scientist was British.

    After thinking of a scientist, a human player provides an incomplete subset of answers that partially identifies the scientist. The player then conveys those clues to the network by plopping DNA strands that correspond to those answers into the test tube.

    These plopped-in strands interact with the neural network, which fires or not depending on its answer. To see the neurons firing, a fluorescent molecular marker lit up when activated.

    In this way, the network communicates via fluorescent signals to identify which scientist the player has in mind or that it has insufficient or contradictory information. The researchers played the game with the network using 27 different ways of answering the questions. It responded correctly each time.

    Beyond playing lab games, the technology has applications for the design of new drugs as well as performing chemical and biological research, the scientists say. For example, biochemical networks designed to go inside a body could help identify a disease and deliver targeted drugs.

    But that future is distant, Qian says. For one, finding a way to get the network to function inside a living organism presents a whole new set of challenges than operating inside the test tube.

    As for creating an artificial human brain with lab-made DNA ... don't worry just yet. The four neuron network took eight hours to identify each mystery scientist. The human brain consists of 100 billion neurons and can make decisions in a split second.

    (Via Discovery News)

    More on artificial intelligence:

    • Beyond 'Jeopardy': Watson wins
    • What will happen when machines outthink us?
    • Scientists work on artificial cat brain
    • Neuron-like computer hardware finally gets software

    John Roach is a contributing writer for msnbc.com. Connect with the Cosmic Log community by hitting the "like" button on the Cosmic Log Facebook page or following msnbc.com's science editor, Alan Boyle, on Twitter (@b0yle).

    2 comments

    There's a fine line between conscience and instinct. I think we have one way to deliver the truth. But after it's fact there is no more instinct and later we will have no emotions about creative thinking. Not knowing and searching on our own time is better than looking in to a glass telescope and as …

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  • 3
    Jul
    2011
    11:10pm, EDT

    Africans visit their American cousins

    Courtesy of William Holland

    Marvin and William Holland, from left, sit beside Ntomnifor Richard Fru during an African-American reunion in June. Genetic analysis suggests that the Holland brothers are distantly related to Fru's Cameroonian family.

    By Alan Boyle, Science Editor, NBC News

    Thanks to 21st-century genetic testing, William Holland is finally able to show some of his African cousins what happened to his slave ancestors back in the 18th century. The climax of Holland's quest came last weekend, when about 60 African-Americans and Africans gathered at Franklin County Recreational Park in Virginia for a teach-in about his family's ocean-spanning, three-century saga.

    The 42-year-old Holland, who lives in Atlanta, left his job at Coca-Cola and turned his focus to the family quest nine years ago. The quest is particularly difficult for African-Americans like Holland because their ancestors came over in chains with their African identity erased. Holland eventually figured out that his great-great-great-great-grandfather was brought over from Africa around 1772 and sold to a Virginia plantation owner. He even discovered that his great-grandfather, Creed Holland, was forced to serve in the Confederate Army during the Civil War.

    But traditional genealogical research couldn't give Holland any further clues as to his African origins. Exactly where did his ancestors come from? Did he have any present-day cousins back in the old country? That's where genetic tests could point the way.


    Holland had his DNA analyzed for markers that just might match up with African kin who had taken similar tests. Records held by the Sorenson Molecular Genealogy Foundation suggested that he might be related to the king of a region in Cameroon's Northwest Province, named Fon Angwafo III. When Holland visited Cameroon and laid out his records for the king and his counselors to inspect, he was welcomed as a long-lost relative. In fact, during a follow-up visit with other family members, Holland was ceremonially named Ndefru, after Fon Angwafo's father.

    The Africans told how they lost their kin during the days of the slave trade — but when the African-Americans told how their ancestors lost their identity through slavery, Holland's Cameroonian cousins just couldn't believe it. So Holland invited "the Fon" and his family to come over to America and learn more about the other side of the slavery story.

    It took months to make all the arrangements, and Fon Angwafo III himself couldn't make the trip because of political obligations at home — but late last month, the Fon's wife, Queen Kiko Anna Angwafo, finally arrived in America along with the king's son and nephew to see the region in Virginia where Holland's ancestor ended up. Holland and his family were the Africans' hosts for a family reunion on June 25. Cameroonians from the Mankon region ruled by the Fon and from the nation's West Region attended the event as well.

    Courtesy of William Holland

    African-Americans and African visitors wear traditional garb at the Frontier Culture Museum's West Africa farm exhibit near Staunton, Va. From left are William (Ndefru) Holland, Regina and Kamari Holland, Marvin (Tsi) Holland, Prince Peter Tseghama Angwafo, Willie Mae (Mankah) Holland, Queen Kiko Anna Angwafo, Ntomnifor Richard Fru and Eric Bryan, the museum's deputy director.

    Courtesy of William Holland

    Queen Kiko Anna Angwafo picks up a pestle at the Frontier Culture Museum's West Africa village exhibit.

    One of the highlights was a visit to the Frontier Culture Museum in Staunton, Va., where a replica West African village has been built to give visitors a taste of life before slavery.

    But the climax came when the Africans were taken to the old Holland plantation, where William Holland's ancestors lived as slaves (and took on the last name of their owners).

    "The whole purpose was to tie in the missing links," Holland told me. And by that measure, he judged the reunion to be a great success. The Cameroonians saw a blacksmith shop from the Civil War era. They soaked in the history as they toured the plantation's old chicken house and slave kitchen. They walked around the graves where slaves and their owners were buried.

    "They totally understood," Holland said. He quoted them as saying, "Now we know you weren't joking around when you told us about this. ... It's very clear now, the pain and suffering you went through when you came to America."

    And there was a bonus: A descendant of the slave owners, John Sherrard Holland, served as the Africans' tour guide.

    Courtesy of William Holland

    William Holland's family and his African visitors meet with John Sherrard Holland, a descendant of the plantation owners who held William Holland's ancestors in slavery.

    "It was a great honor and a pleasure to do that," the 55-year-old operator of a hunting preserve told me later. He went to school with members of William's family, and "we've always had the best of relationships," he said.

    As for the dark past of slavery, John Sherrard Holland said that has been left far behind. "It's history," he said.

    But William Holland said that history is worth reflecting upon once more, particularly at a time when America is celebrating Independence Day. He noted that when Americans heralded their freedom in 1776, his African ancestor had been unfree for four years. "Just imagine what he was thinking," Holland said.

    "Is it time for celebration?" he asked. "I don't know. But now we're trying to do justice to that heritage — and that's something to celebrate."

    Previous chapters in the tale of William Holland's roots:

    • Sept. 8, 2010: DNA points to royal roots in Africa
    • Feb. 1, 2011: Family roots get tangled up in Africa
    • Feb. 28, 2011: Black history saga comes full circle 
    • African American news from theGrio

     For further information about genetic testing for genealogical purposes, check out this guide on Cyndi's List, or this entry on Wikipedia. If you happen to be a Boyle looking for genealogical information, take a look at my Boyle family website. You can also connect with me via Facebook or Twitter. And if you really want to be friendly, ask me about "The Case for Pluto."

    17 comments

    did the Africans apologize for selling their cousins into slavery?

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  • 15
    Apr
    2011
    4:12pm, EDT

    DNA origami goes 3-D

    The Biodesign Institute Arizona State University

    Figure 1 a and b display schematics for 2-D nanoforms with accompanying AFM images of the resulting structures. 1 c-e represent 3D structures of hemisphere, sphere and ellipsoid, respectively, while figure 1f shows a nanoflask, (each of the structures visualized with TEM imaging).

    By John Roach, Contributing Writer, NBC News

    Earlier this week, we learned about wedding rings made out of DNA. Now, the ability to fold stringy bits of DNA into patterns and shapes has gone 3-D thanks to a new technique pioneered at Arizona State University's Biodesign Institute.

    The breakthrough, reported in the April 15 issue of Science, is a step on the road to eventually using the procedure to create diminutive drug delivery devices, nano-computers, and chemical factories.


    So-called DNA origami was introduced in 2006 by Paul Rothemund of the California Institute of Technology. It hinges on the self-assembling properties of DNA's four complimentary base pairs, which form the famous double helix.

    These nucleotides, labeled A, T, C and G, follow a formula of how they interact. A always pairs with T and C with G. DNA origami practitioners exploit this base pairing to create complex shapes, but until now most shapes were two dimensional.

    To do this, they frame the desired shape with a length of single-stranded DNA and then use DNA "staple strands" to cross over and integrate the structure and hold the desired shape.

    "Our goal is to develop design principles that will allow researchers to model arbitrary 3-D shapes with control over the degree of surface curvature," Yan Liu of the Biodesign Institute, said in a news release explaining the research.

    "In an escape from a rigid lattice model, our versatile strategy begins by defining the desired surface features of a target object with the scaffold, followed by manipulation of DNA conformation and shaping of crossover networks to achieve the design."

    To achieve this, the team starts with simple, 2-D concentric ring structures formed from a DNA double helix and bound together at strategically placed crossover points. Varying the number of nucleotides between crossover points allows the designer to combine sharp and rounded elements into 2-D and 3-D forms.

    More on tricks with DNA:

    • 'Wedding Rings' made out of DNA
    • Slideshow: Making smiley faces from DNA
    • DNA robots pave way for microscopic factories 
    • DNA twisted into pretzels
    • Play a game and engineer real RNA 

    John Roach is a contributing writer for msnbc.com. Connect with the Cosmic Log community by hitting the "like" button on the Cosmic Log Facebook pageor following msnbc.com's science editor, Alan Boyle, on Twitter (@b0yle).

    5 comments

    Just as long as we don't accidentally, or on purpose, create a virus like pathogen.

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  • 11
    Apr
    2011
    6:44pm, EDT

    'Wedding rings' made out of DNA

    Alexander Heckel

    The world's smallest wedding rings are built up from two interlocked strands of DNA.

    By Alan Boyle, Science Editor, NBC News

    Thorsten Schmidt can now say he had a hand in creating the world's smallest wedding rings, measuring less than a thousandth of the width of a human hair.

    The interlocked rings, known as catenans (after the Latin word for "chain"), were made from looped strands of DNA and measure just 18 nanometers wide. The wedding angle comes about not only because of the rings' perfectly circular shape, but also because Schmidt got married while he was working on the experiment.


    These rings aren't just a romantic gesture: Because they're freely pivotable, they could be useful components in nano-machines or molecular motors.

    "We still have a long way to go before DNA structures such as the catenan can be used in everyday items," Professor Alexander Heckel, Schmidt's co-author and adviser at Germany's Goethe University Frankfurt, said in a news release, "but structures of DNA can, in the near future, be used to arranage and study proteins or other molecules that are too small for a direct manipulation, by means of auto-organization."

    Heckel and Schmidt / ACS Nano Letters

    An atomic force miroscope image shows the interlocked DNA rings, along with an illustration showing how they're chained together.

    The experiment, reported in the journal Nano Letters, involved creating two C-shaped DNA fragments that were positioned with their open ends pointing away from each other. Polyamide bonds were attached to the DNA to anchor the fragments to each other, and then the researchers added an oligonucleotide to close each of the C-sections and form the rings. The operation was done with mere chemistry. No nanometer-sized tweezers were required.

    The paper notes that the assemblages resemble "stylized wedding rings," and here's the icing on the cake: Schmidt, who is now at Harvard's Wyss Institute for Biologically Inspired Engineering, dedicated the paper "to his wife and colleague Dr. Diana P. Goncalves Schmidt on the occasion of their wedding." Let's see Prince William top that one!

    More tricks with twisty molecules:

    • DNA folded into a world of patterns
    • Slideshow: Making smiley faces from DNA
    • DNA robots pave way for micro-factories
    • The latest twist: Pretzels made of DNA
    • Play a game and engineer real RNA

    Join the Cosmic Log community by clicking the "like" button on our Facebook page or by following msnbc.com science editor Alan Boyle as b0yle on Twitter. To learn more about my book on Pluto and the search for planets, check out the website for "The Case for Pluto."  

    3 comments

    It's the devil, mama

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  • 23
    Nov
    2010
    3:12pm, EST

    New blood test can determine age

    Paula Bronstein / Getty Images file

    A new test can determine a person's age to within nine years from a drop of blood.

    By John Roach, Contributing Writer, NBC News

    Crime scene investigators with little more to go on than a drop of blood have a new test that can help them determine the age of the person who was bleeding, according to a study in today's issue of Current Biology.

    The test will work even on dried bloodstains -– perhaps even those revealed by a heat-vision camera. This could help detectives reopen cases that went cold years ago. And it's only a matter of time before screenwriters start working the technology into the plotlines for "Law and Order" or "C.S.I."

    The technique, developed by scientists at Erasmus MC University Medical Center Rotterdam in the Netherlands, is based on the fact that certain DNA molecules in some blood cells decrease with age, TG Daily reports:

    "The molecules used are residues of the immune system known as sjTREC molecules. These special DNA molecules are released in blood cells as a result of the adaptations that have to be made by newly formed specific immune cells -- T cells -- to recognize bacteria, viruses, parasites or possibly cancer cells. Their number decreases with age."


    The age test is accurate to within nine years. That should be sufficient to place unknown people –- criminals or missing persons, for example -– into generational categories spanning about 20 years.

    Study co-author Manfred Kayser, a professor of forensic molecular biology, said in a news release that this is a harbinger for what's to come, as researchers uncover new methods designed to reconstruct the appearance of unknown persons from biological samples at crime scenes.

    One test, for example, can determine eye color from DNA and has already been put to forensic use.

    "Conventional DNA profiling applied in forensics can only identify persons already known to the investigating bodies, because the approach is completely comparative," he said. In cases where the DNA at the scene doesn't match any known suspect tested, "it is expected that appearance information estimated from evidence material will help in finding unknown persons."

    More about the forensic frontier:

    • New camera 'sees' invisible blood stains
    • Cat fur puts criminals behind bars
    • Crime labs cut to the bone
    • Readers, pick your poison

    John Roach is a contributing writer for msnbc.com. Connect with the Cosmic Log community by hitting the "like" button on the Cosmic Log Facebook page or following msnbc.com's science editor, Alan Boyle, on Twitter (@b0yle).

    14 comments

    Well, obviously the monkey wrench that could be thrown into this new forensic technique is if the researchers also find a way to keep T cells at youthful levels in older people as a result of their research.

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  • 29
    Sep
    2010
    10:26pm, EDT

    How cheaper genomes fuel science

    NIEHS

    DNA's double helix encodes information that could have medical application.

    The cost of whole-genome sequencing is dropping like a rock, and that’s fueling a “renaissance of activity” for scientific sleuths tracking down the genetic causes of disease, a pioneer in the field says.

    Harvard geneticist George Church provided a status report on the genome market, and its implications for medical research, during this week's "Open Questions in Neuroscience" symposium in Seattle, sponsored by the Allen Institute for Brain Science. Church is not only a Harvard professor and research, but also the founder of the Knome commercial venture for genome-sequencing.

    Thanks to competition in the sequencing field, the price of decoding a complete human genome has been following an affordability curve that looks like Moore's Law on steroids. The cost of the federal Human Genome Project, which issued its first draft in 2000 and a complete genome sequence in 2003, was estimated at $2.7 billion in 1991 dollars. But that price tag has been falling by as much as an order of magnitude per year, and today the going rate for whole-genome sequencing is edging below $10,000 (counseling costs extra). The cost of materials — that is, the chemical reagents required to do the tests — is merely $1,000, Church said in June.

    That might suggest that the goal of the $1,000 genome could be achieved in the next year, but Church told me there might be a price plateau instead. In any case, the rapid price decline is reviving hopes that DNA tests can reveal which combinations of genes are linked to extreme or distinctive traits.

    Church pointed to the example of Charcot-Marie-Tooth syndrome, a disease that affects nerve function in the body's extremities. In March, researchers at the Baylor College of Medicine announced that they unraveled the genetic cause of the disease by sequencing the entire genome of a sufferer (who happened to be a Baylor geneticist) and comparing genetic mutations with those found in his parents and siblings. Another study at the Institute for Systems Biology concluded that no more than four genes were responsible for another rare disease known as Miller syndrome, thanks to whole-genome sequencing for a family of four.

    To accelerate the genomic renaissance, Church established the Personal Genome Project, which is aimed at producing a publicly available database of genome sequences linked to medical data. So far, 16,000 volunteers have signed up, and the project has the go-ahead to sign up as many as 100,000. But less than two dozen people have made their complete genome public. One reason for that is the concern over privacy. But Church told me the biggest reason why more people aren't already "Personal Genome Pioneers" is because of the cost. Sounds like that situation could change pretty darn quickly.

    "Open Questions in Neuroscience" also included presentations by:

    • Susumu Tonegawa, a Nobel-winning neurobiologist at the Massachusetts Institute of Technology who focuses on the genetic and chemical mechanisms that underlie learning and memory.
    • Stephen Smith, a physiologist at Stanford University whose lab explores the brain's microcircuitry and molecular architecture.
    • Olaf Sporns, a neuroscientist at Indiana University whose research centers on designing computational models of neural circuits.
    • Karel Svoboda, a biophysicist at Howard Hughes Medical Institute's Janelia Farm Research Campus who observes neurons at work within mouse brains.
    • Doris Tsao, a biologist at Caltech who concentrates on the brain mechanisms behind image recognition and 3-D perception.
    • Catherine Dulac, a Harvard biologist who studies the olfactory system as well as the processing of pheromone cues.

    Check out the full list of postings from the brain symposium. Join the Cosmic Log corps by signing up as my Facebook friend or hooking up via Twitter. And if you really want to be friendly, ask me about "The Case for Pluto."

    6 comments

    The book "Getting Back To The American Dream" talks about a project called "Minerva Medica". If getting the price down for a genome is important to healthcare it would likely happen quickly if that kind of project was actually of interest to politicians.

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  • 8
    Sep
    2010
    9:58pm, EDT

    DNA points to royal roots in Africa

    Courtesy of William Holland

    DNA testing led Atlanta genealogical researcher William Holland to Cameroon in search of his roots.

    William Holland, a genealogical researcher living in Atlanta, has seen some pretty strange twists in his family tree. Several years ago, he found out that his great-grandfather was a black slave ... who wound up serving as a Confederate soldier during the Civil War. But this year Holland's research resulted in something even stranger.

    Thanks to DNA testing, Holland is being welcomed as a long-lost relative by a ruling family of the West African nation of Cameroon. He's visited the country once already, back in March, and he'll be getting the royal treatment in November when he goes back with additional members of his family, including his 79-year-old mother.

    "Imagine receiving that news, after all these years when you grew up as the son of a sharecropper. ... Everybody tells you that you came from slaves, you came from slaves. And now you find out that you came from royalty," Holland told me.

    Holland's case shows how genetic genealogy can untangle mysteries in a family tree — even for African-Americans, who typically face tougher challenges because the vital records for slaves are so scant.

    Holland attributes his success to GeneTree, a Utah-based DNA testing service that came up with the Cameroon connection. But GeneTree's chief scientific officer, geneticist Scott Woodward, said Williams' case was far from unusual.

    "This isn't our home run," Woodward told me. "It takes a lot of regular work. But what [the DNA analysis] did do was give us some nice clues and hints about where he should concentrate his efforts. Should he be looking in Cameroon, or should he be looking in Nigeria? That makes a big difference."

    In fact, previous genetic tests had indeed suggested that Holland's African roots went back to Nigeria — so much so that Holland arranged for some of his supposed Nigerian relatives to get tested as well. "When the results came back, it wasn't a match," Holland said. (I can sympathize with that situation: Nine years ago, I went down a similar blind alley in search of my Irish roots.)

    So Holland went back to the drawing board. This time, Holland plugged his genetic markers into a database provided by the Sorenson Molecular Genealogy Foundation, which draws upon GeneTree results as well as global genetic surveys.

    Unlike whole-genome sequencing or paternity tests, genealogical testing generally looks at only a limited number of DNA markers — either on the Y-chromosome, which is passed down from fathers to their sons; or in mitochondrial DNA, which is passed down from mothers to their children. Such markers can't be used to figure out your susceptibility to disease or even trace all your relatives. It can only give you an idea who you're related to along your all-paternal or all-maternal line of ancestry.

    The freely available Sorenson database takes the family search to an extra level, by linking the genetic data with traditional pedigrees contributed by those who have been tested. What's more, Sorenson's researchers — including Woodward, who serves as the foundation's executive director — have added test results from places around the world that would otherwise be poorly represented in genetic databases. For example, about 12,000 of the 110,000 DNA samples in the Sorenson files have come from Africa.

    "Most are centered in western Africa, because we believe that's the most interesting, particularly for African-Americans," Woodward said. "We've sampled literally hundreds of different villages throughout these countries."

    In Holland's case, the best matches all landed in Cameroon. "That's what got William excited about pursuing and checking some of those places," Woodward said.

    Armed with detailed pedigrees that linked up with the genetic matches, Holland headed out to Bamenda, the capital of Cameroon's North West Province and the place where the chief of the region's Mankon people has his palace. Holland discussed his family tree with tribal leaders in Bamenda, and eventually was received by the Mankon chief, His Royal Highness Fo Angwafo III.

    "He was so surprised," Holland recalled. "He gave me about an hour of his time. He looked at me, and he just couldn't believe it. He told me, 'William, you could be my son.'"

    During the month that followed, local elders pored over all the records that Holland had prepared. Then they called him in to hear the verdict. "With all the pedigrees you show, you belong to the royal family," Holland said he was told.

    Other research has helped fill in the historical gaps: Historians say that only a few ships were involved in the slave trade between Cameroon and Virginia in the early 1770s, the time frame during which Holland's ancestors came to the colonies. "I think I may have the actual ship that brought us to America. The Cambridge sailed in 1771. The Fox sailed in April 1772. I think that was the one," he said.

    Today, the 41-year-old Holland is working to renovate the family homestead in Virginia, where slaves once lived. He's also working to get his complete family history in order — and encouraging others to go on their own family quest.

    "We all come from different parts of the world, but this is how we come together," Holland told me.

    Meanwhile, Woodward and other researchers are working to develop new genetic tools for tracing family connections. One method would check markers on additional chromosomes to "fill in close relatives, we're thinking within four to six generations, and reconstruct a relationship between two individuals who share a common ancestor," Woodward said.

    "That's not even in beta. It's in alpha," Woodward told me. "It essentially covers all of your ancestors."

    That could mark a significant leap forward for genetic genealogy. The tests conducted on Y chromosomes or mitochondrial DNA aren't powerful enough to detemine the precise relationship between two individuals. But when they're accompanied by hard work and personal contacts, even those tests are clearly powerful enough to forge an ocean-crossing link between an African chief and the son of a sharecropper.

    "They're planning a huge welcome-home party for us in November," Holland said of his newfound family in Cameroon. "They consider us the lost children. There will be a lot of cooking, a lot of celebrating. ... You better get ready. This is something not to miss."

    More about Africa and genealogy:

    • She traces genetic 'Roots' to Africa
    • An Irish tale: The wearin o' the genes
    • Genealogy news from msnbc.com
    • African American news from theGrio

    GeneTree is just one of many companies offering genetic testing for genealogical purposes. For further information about services and pricing, check out this guide on Cyndi's List, or this entry on Wikipedia. If you happen to be a Boyle looking for genealogical information, take a look at my Boyle family website. (Yes, I know it's in need of an update.) You can also connect with me via Facebook or Twitter. And if you really want to be friendly, ask me about "The Case for Pluto."

    14 comments

    Good work guys. Congratutaltions guys. All the blacks in America are mainly west Africans. It really doesent matter if you are from a royal family or not. Basically, this is not just about having a well to do background, afteral, there a lot of richer family than the royal families. Whatever you ba …

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  • 7
    Jul
    2010
    9:11pm, EDT

    How a son's DNA snared his father

    Calif. Attorney General's Office

    A criminalist conducts DNA testing at a California lab.

    Today's arrest in the "Grim Sleeper" serial-killing case demonstrates how the sins of the father can be found out through a son's DNA - and why the technique can be controversial.

    A 57-year-old one-time LAPD garage attendant named Lonnie Franklin Jr. was arrested in Los Angeles in connection with the string of 10 murders, committed between 1985 and 2007. The killer was nicknamed the "Grim Sleeper" because there was a 14-year break within that string, from 1988 to 2002.

    The case puts an unorthodox forensic tool known as familial DNA analysis at center stage. The method is specifically allowed only in two states - California and Colorado - and it's specifically banned in Maryland. New York is OK with using the method, but only if it's an "inadvertent" side effect of a more rigorous data search. The FBI currently has no firm policy on familial DNA matching but is willing to let states share their DNA data for use in the procedure.

    Now that familial DNA analysis has come up with a high-profile match, you'll probably be hearing much more about whether it should be used more widely.

    Not-quite-perfect match
    Why is the technique so controversial? It's because investigators look for not-quite-perfect matches between the DNA left behind at a crime scene and DNA markers taken from a wide sampling of people who may or may not have committed a crime themselves. The goal isn't necessarily to find the suspects, but rather the potential relatives of suspects. If there's a close match, investigators could focus their search on close relatives of the person who matched up - in hopes that the trail will lead to suspects who haven't left a DNA trail themselves.

    It's basically a crime-lab variant of the tests widely used to trace your genealogy, but these would be relatives you might not want to feature on your family tree.

    Familial DNA searches have been done in Britain for years, and California Attorney General Jerry Brown gave investigators the go-ahead to do the same in the Grim Sleeper case two years ago. A database search came up with a partial but significant match between DNA collected during the investigation and a routine sample taken from Franklin's son. Brown said the son was given a cheek swab after his conviction on a felony weapons charge. LA Weekly reported that the results of the DNA analysis "lit up like a Christmas tree."

    The investigators followed up by snagging DNA samples from Franklin himself. A relative of one of the Grim Sleeper victims who was briefed by police said that the sample was left on a restaurant cup, while the Los Angeles Times reported that the DNA was recovered from a discarded piece of pizza. The most likely scenario is that forensic sleuths tested the pizza, the cup and any other items that Franklin might have put to his lips while dining.

    District Attorney Steve Cooley told the Times that the arrest "shows the legitimacy" of using partial DNA matches and promised to provide more details at a Thursday news conference.

    If the arrest leads to a conviction, the feat will take forensic genetics to a whole new level. But it could raise a whole new crop of questions about genetic privacy as well.

    Lifetime genetic surveillance?
    In California, for example, the DNA samples are collected after every felony arrest, and may be retained even if the suspect later goes free. That has sparked a legal challenge from the American Civil Liberties Union. The ACLU noted that about a third of all those arrested for felonies in California are not convicted of any crime, and said that "thousands of innocent Californians will be subject to a lifetime of genetic surveillance because a single police officer suspected them of a crime."

    The ACLU also said the system could have a "huge racial impact" because a disproportionate number of people of color are already represented in California's criminal justice system, which serves as the main channel for the state's DNA sampling flow (at a rate of roughly 25,000 samples per month). The latest figures show that California has the biggest statewide DNA database in the country, with more than 1.5 million samples. ACLU calls it the third-biggest forensic DNA database in the world, behind the FBI's nationwide CODIS system (which includes the California samples) and Britain's national data bank.

    We're right in the midst of a massive crime-lab experiment in DNA collection. The federal government and all 50 states require those convicted of felonies to provide DNA samples, but California is just one of the 23 states that require DNA for felony arrests. Congress and several states, including New York and North Carolina, are currently talking about widening their DNA collection programs to cover arrests as well as convictions.

    Proponents of wider DNA testing say that such measures will prevent crime, save lives and provide more protection to the innocent. Opponents say that such measures will put more of a burden on the innocent, and that familial DNA analysis could turn even distant relatives into "genetic informants." I say that the Grim Sleeper case will increase the pressure on lawmakers to bulk up DNA databases across the country, and will lead to wider use of familial DNA as well. Is that a good thing, or a bad thing? What do you say? Weigh in on this issue by leaving a comment below.

    More on genetic sleuthing:

    • Who's keeping your genetic keys?
    • Interactive: Your genetic fingerprints
    • DNA collection raises ethical questions
    • Gaps in DNA databanks lead to tragedy
    • DNA pioneer wants cuts to criminal database

    Join the Cosmic Log corps by signing up as my Facebook friend or hooking up on Twitter. And if you really want to be friendly, ask me about "The Case for Pluto."

    115 comments

    I thought I had a constitutional right to not incriminate myself. What could be more "me" than my dna? We already sniff each others urine like dogs in pre-employment drug screening. The dna databases are used for crime now, but what about in the future? California is broke, how much is a dna databa …

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John Roach is a contributing writer for NBC News. From climate change and mass extinctions to human evolution and deep space, his writing explores life on Earth and its place in the universe. He was a staff writer at the Environmental News Network for several years and has contributed to National Geographic News for more than a decade.

Alan Boyle, Science Editor, NBC News

Science editor at msnbc.com, author of "The Case for Pluto," winner of the National Academies Communication Award for Cosmic Log in 2008. Alan Boyle covers the physical sciences, anthropology, technological innovation and space science and exploration for msnbc.com. Check out Cosmic Log's archives by following the links below, and see Boyle's full biography at http://bit.ly/boyle-bio

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