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Category Archives: Transhuman News

Use of force may be applied to collect DNA samples from inmates … – Beatrice Daily Sun

Posted: June 23, 2017 at 5:49 am

A Lincoln judge has given the OK for the Nebraska Department of Correctional Services to use reasonable force to collect DNA from an inmate refusing to give it voluntarily.

It was the fifth time the state prison system had sought permission to use force to get DNA samples from the 78 inmates who still hadn't provided it to prison staff as of February.

The other motions were in Omaha cases. One since has led to new charges against Brandon Weathers in connection to serial rapes of four women in 2002 and 2004.

DNA can be an important tool used to solve crimes or lead to suspects.

The Nebraska Attorney General's office recently asked a Lincoln judge for an order to allow a Phoenix police officer to get an additional DNA sample from an inmate at the Nebraska State Penitentiary.

After the inmate went to prison in September for a sex assault in Douglas County, his DNA sample was collected.

In December, the Nebraska State Patrol Crime Laboratory matched his DNA, which was uploaded into the Combined DNA Index System, to DNA on a toothbrush taken from a Phoenix home in 2010 by investigators looking into the homicide of a man who had been shot dead in a car outside, according to court records.

State law says a person who had been convicted of a felony or other specified offense as of July 15, 2010, who did not have a sample in the state DNA Sample Bank, was required to have one collected at his or her own expense. The law also applied to people already serving a sentence.

Still, some inmates refused to comply.

In the Lincoln case, Assistant Nebraska Attorney General Kale Burdick said prison employees notified Reuben J. Reyes of his obligation to provide his DNA in April 2013, about two months after he went to prison, and again this May.

Reyes refused, Burdick said in the motion filed June 14.

The same day, Lancaster County District Judge Lori Maret authorized the use of force to get it from the man serving a 20- to 25-year sentence for attempted first-degree assault and use of a firearm to commit a felony for pointing a .380 handgun at his cousin and firing once into the air, then twice more in his cousin's direction, in 2012.

Lincoln police said one of the rounds hit an apartment building. Another hit a car.

Reyes later pleaded no contest.

By Monday, state prisons spokeswoman Dawn-Renee Smith said the number of inmates who hadn't provided DNA was down to six.

She said she couldn't provide a list of the inmates' names because the information is related to their conduct in prison and protected by state statute.

Earlier this month, Corrections Director Scott Frakes said he is committed to collecting DNA samples from every incarcerated person to be in full compliance with state statute.

By policy, inmates who have not provided a DNA sample are ordered to submit it monthly and get written up for each refusal. Misconduct reports that result are referred to the institutional disciplinary committee.

Repeated refusals can lead to up to 90 days of lost good time.

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DNA nanomachines can transmit information – Cosmos

Posted: at 5:49 am

One of the DNA nanomachines and the shapes it can switch between.

Song et al.

DNA-based computers are one step closer to full realisation following the creation of simple DNA machines that can switch between two shapes with only a single trigger.

The switching ability, which is fully reversible, means that information is being relayed at a molecular level transferred between DNA structural units in a manner than is both self-sustaining and controllable.

Lead researcher Yonggang Ke of the Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech, US, says the micromachines can be used to either relay specific pieces of information through a DNA-constructed system, or to amplify a signal emanating from another part of it.

In the field of DNA-based computing, the DNA contains the information, but the molecules are floating around in solution, Ke says.

Whats new here is that we are linking the parts together in a physical machine.

Ke and colleagues constructed two different nanomachines, each comprising a number of artificial DNA double helixes stacked on each other, in two orientations, providing strength and stability.

The completed design looks rather like an accordion, or a foldable trellis.

One extra strand at the edge of each machine is attached, and functions as a trigger. When activated it compels the first DNA strand of the machine array to contract (or expand, depending on its initial state). This in turn transfers energy to the next strand, causing it to move in the same way, and so on, a little like dominoes falling.

The machines, fully built, are just a few hundred nanometres long slightly smaller than an influenza virus. To see them, Ke and colleagues used a powerful imaging technique known as atomic force microscopy.

Constructing machines on a nanometric scale would seem to require some impossibly fine hand-eye coordination on the part of the molecular engineers, but the compulsion of DNAs chemical structures to automatically bond means that, in solution, they seek out the complimentary strands of their neighbours, making construction a guided, rather than mechanical, process.

Although the machines built by Ke and his colleagues are very simple, they provide a powerful pathway towards construction of more complex structures. In research published in the journal Science, the team include blueprints for rectangles, cubes and tubes built by the same process.

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Brain-Invading Tapeworm That Eluded Doctors Spotted by New DNA Test – Scientific American

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Doctors at Zuckerberg San Francisco General Hospital could not figure out what was wrong with the 29-year-old man sitting before them. An otherwise healthy construction worker from Nicaragua, the patient was suffering from a splitting headache, double vision and ringing in his ears. Part of his face was also numb. The cause could have been anythingfrom an infection to a stroke, a tumor or some kind of autoimmune disease. The Emergency Department (ED) staff took a magnetic resonance imaging scan of the mans brain, performed a spinal tap and completed a series of other tests that did not turn up any obvious reason for the swelling in his braina condition that is formally known as encephalitis.

Most likely, it was some kind of infection. But what kind? Nineteen standard tests are available to help clinicians try to pin down the source of encephalitis, but they test for the presence of only the most common infections; more than 60 percent of cases go unsolved each year. Physicians looked in the patients cerebrospinal fluid (which surrounds the brain and protects it) for evidence of Lyme disease, syphilis and valley fever, among other things. Nothing matched. So the S.F. General ED staff settled on the most likely culprit as a diagnosis: a form of tuberculosis (TB) that causes brain inflammation but cannot always be detected with typical tests. Doctors gave the man a prescription for some steroids to reduce the swelling plus some anti-TB drugs and sent him home.

Soon he was back, however, with the same symptoms. This time the physicians assumed the man, whose life was chaotic, had not been taking his drugs properly. (Even people with regular jobs and schedules often find taking TB medications fairly difficult.) The ED staff sent him away with another prescription but he returned again and againeven after he could prove that he was taking his medication correctly and on time. The drugs helped briefly after each visit, but the symptoms always returned. During that year his medical bills reached $580,000. Finally, S.F. General turned to an experimental test that is designed to uncover the source of virtually any neurological infection.

The test is the brainchild of researchers at the nearby University of California, San Francisco, led by neurologist Michael Wilson, biochemist Joseph DeRisi and infectious disease expert Charles Chiu. The group uses genetic-sequencing technology to identify mystery illnesses in people with encephalitis or meningitis (inflammation of the meninges, the membranes around the brain and spinal cord). This so-called metagenomic test analyzes all the DNA and RNA found in a sample of cerebrospinal fluid (meta means beyond in Greek). So any DNA or RNA that does not belong to the patientincluding that from viruses, bacteria, parasites or fungishows up in the results.

Done correctly, metagenomic testing could radically change the way infections of the brain are diagnosed. An element of circular logic underlies most standard infectious disease tests. Doctors order individual tests for each bug they suspect might be causing the problem. But how do they know what is causing the problem if they have not yet done the test? Metagenomic sequencing, in contrast, casts the broadest possible net, which allows it to pick up unexpected or previously unknown pathogens. Were looking at everything at once, which has the potential of replacing the myriad of lab tests with a single test, Chiu says.

The U.C. San Francisco team ran a sample of the mans cerebrospinal fluid through their investigative diagnostic procedure. Thats when we found the worm, Wilson says. Genetic sequencing and analysis revealed DNA from the kind of tapeworm found in pigs. The patient did not get better on TB drugs because he did not have TBhe had tapeworms living in his brain.

In Nicaragua and other developing countries tapeworm infections are common, and the larvae can migrate into the braina condition called neurocysticercosis. Usually the infection causes seizures as well as large brain cysts that are obvious on an MRI. This man had neither, however, which had led the medical staff to dismiss neurocysticercosis as a possibility. When this guy first presented, they absolutely thought of it, Wilson says. But when they scanned him in his brain and spinal cord, there were no cysts. He would improve briefly, because the steroids they gave him temporarily reduced the swelling in his brain, but the TB drugs were useless, so he would soon relapse again. Now that they knew the cause, the team started him right away on anti-worm drugs, which cannot eliminate the infection but will keep it under control. Its very treatable, Wilson says. Hes doing great.

The construction worker is one of nearly 300 patients who has participated since June 2016 in a metagenomic sequencing study based at U.C. San Francisco. Participants consist of anyone who has been admitted to one of eight medical centers, mostly in California, with an apparent neurological infection and no clear diagnosis. Metagenomic sequencing is done alongside traditional testing, for a head-to-head comparison.

Wilson and colleagues hope to prove their test, which will be more widely available this summer for about $2,400, can be an efficient and reliable solution for the sorts of medical mysteries that befuddle doctors, aggravate patients and can run up huge medical bills. The challenge is in making sense of the output, Chiu says. Sequencing does not produce a yes or no answer. The group developed a standard set of procedures to make it easy for an infectious disease doctor to pinpoint what the most likely bug might be.

On July 1 the U.C. San Francisco group will begin offering this test as a custom-ordered service to a broader group of people so that hospitals and labs in the U.S., and eventually anywhere in the world, can send cerebrospinal fluid for analysis. They plan to eventually expand their metagenomic testing to include pneumonia (infection of the lungs) and sepsis (infection of the bloodstream)two other ailments that often cause diagnostic dilemmas.

A similar metagenomic test for pneumonia, developed by researchers at the University of Utah, Arup Laboratories and start-up IDbyDNA, is also expected to debut this summer. In both cases the teams first do extensive work to make it easier for physicians to understand the complex and ambiguous genomic information garnered by the test.

These two tests will be the first commercially available metagenomic tests for infection in the U.S., but they are part of a growing trend. Two academic groups in Europe recently introduced tests for sepsis. And researchers at computational geneticist Pardis Sabetis lab at Harvard University are currently running a study on a similar test for encephalitis, says Anne Piantadosi, an infectious disease physician at Massachusetts General Hospital and a postdoctoral research fellow with the Sabeti group. She envisions a time in the next few years when future clinicians will be able to look back say, That was a really big improvement in how we diagnose infections.

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FootJoy introduces DNA Helix shoe – Golf Channel

Posted: at 5:49 am

FootJoy has launched the latest version of the DNA (DryJoys Next Advancement) franchise, the DNA Helix.Featuring a wider platform and a lightweight construction to create power from the ground up, DNA Helix is available on footjoy.com and wherever FootJoy golf shoes are sold.

DNA Helix was developed based on specific feedback from the worlds best players who value the combination of flexibility and comfort but requested more platform stability, particularly in the heel area of the shoe.

Ive worn every version of DNA and this is by far the best for me, said Scott Stallings. The additional support they built in, especially laterally as I move back and through the ball, is fantastic.

The new NitroThin 3.0 TPU (thermoplastic polyurethane) outsole foundation in DNA Helix was developed to deliver the additional stability requested by Tour players. In fact, FootJoy says DNA Helix is 38 percent more stable than its predecessor. This was achieved by increasing the width between the cleat receptacles in the heel by 13 percent for more surface coverage. In addition, a new fit-bed was developed with more lateral stability and the integration of a 3D FoamCollar also helps to lock the players foot in place.

The new outsole also features strategically placed cut-outs in the TPU to expose more of the softer midsole which contributes to this outsole being 23 percent lighter than the previous version as well as being more flexible.

While it was certainly a challenge to improve upon a shoe as successful as DNA, the continued dialog we have with our Tour staff revealed there was an opportunity to improve the overall performance of the category, said Keith Duffy, Senior Product Manager, Footwear. But this isnt just an update for us. DNA Helix is a completely new golf shoe built from the ground up to deliver Tour-level performance and lightweight comfort for all players.

DNA Helix comes with a two-year waterproof warranty. Suggsted retail price is $209.99 (laced) or $239.99 (Boa System).

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Water treatment could be damaging DNA – The Hippocratic Post (blog)

Posted: at 5:49 am

Water treatment is vital to maintain human health but a method widely used in developing countries could be damaging the DNA of those drinking it. Despite poor evidence of their effectiveness as a water disinfectant, colloidal silver and silver nanoparticles are increasingly being promoted for treating potentially contaminated drinking water in low income countries.

Despite poor evidence of their effectiveness as a water disinfectant, colloidal silver and silver nanoparticles are increasingly being promoted for treating potentially contaminated drinking water in low income countries.

A study led by the University of East Anglia has concluded that there is a risk these treatments could in fact cause genotoxicity, which is damage to DNA, and affect reproduction and future generations. Prof Paul Hunter from UEAs Norwich Medical School, said the study brings together existing research to highlight the potential risks. Colloidal silver as a water treatment is sold across Africa and in countries like Haiti, despite the fact it doesnt treat water very effectively. The World Health Organization (WHO) advises against its use as a primary water treatment. If it isnt doing any good, we wanted to investigate if in fact it could be causing harm. The research looked at previous studies where the effects of silver, silver nitrate and silver nanoparticles have been measured in vivo on living animals. They found that, although results varied, more studies than they expected showed some evidence of genotoxicity, reporting effects including chromosomal aberrations, DNA fragmentation and damage to sperm. Prof Hunter said: We already know that there is little evidence that silver in water has any benefit. But this study brings together a body of work which shows it is potentially damaging DNA, and harming reproductive success. Colloidal silver is also widely marketed as an alternative health substance which can treat everything from skin complaints to bacterial and viral infections, cancer and AIDS. Again, little research exists to show any beneficial effects, but there are known side effects. One of the more obvious signs of over-exposure to silver is argyria, where the skin and hair turns a blue-grey colour.

One of the more obvious signs of over-exposure to silver is argyria, where the skin and hair turns a blue-grey colour.

WHO guidelines for drinking water quality dont currently include a value for silver in water, but indicate that a concentration of 0.1 milligrams per litre could be tolerated without risk to health. However, this was determined as a level unlikely to cause argyria, and didnt take into account potential damage to DNA. Prof Hunter said: While none of the previous studies alone are definitive, and we cant use them to determine a safe level of consumption from this review, we consider that the balance of evidence suggests there is the chance of damage to DNA. There is an urgent need for more research on this area to determine if people drinking water treated with silver have evidence of DNA damage.

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Long-read sequencing ‘illuminates’ previously inaccessible parts of … – FierceBiotech

Posted: at 5:49 am

Since the Human Genome Project concluded in 2003, genome sequencing has become cheaper and more accessible. But currenttechnology has its limitations. Now, for the first time, Stanford University researchers have used long-read, whole genome sequencing to diagnose a patient.

Sequencing a genome involves determiningthe order of nucleotide base pairs, or letters, in that individuals DNA. This is done by snippingDNA into pieces that a sequencer can read, and then using a computer to put these fragments in order.

Current short-read technology chops DNA up into words that are about 100 letters long.Long-read sequencing makes wordsthat can be thousands of letters long, said Euan Ashley, the studys senior author and a professor of cardiovascular medicine, genetics and biomedical data science at Stanford, in a statement.

This allows us to illuminate dark corners of the genome like never before, Ashley said. Cutting up DNA into smaller pieces means there are more breaks between individual segments. Some parts of the genome can be missedabout 5%of it, the researchers wrote. Any mutationsdeletions or insertionsthat exceed a certain length are undetectable with short-read sequencing.

The Stanford team used long-read sequencing to make a diagnosis for Ricky Ramon, a patient whose symptoms pointed to Carney complex, a rare genetic condition caused by mutations in the PRKAR1A gene. But short-read sequencing found no disease-causing gene variants in Ramons genome.

Carney complex is characterized by an increased risk for several types of tumors, including benign tumors in the heart. Ramon has undergone multiple surgeries to remove these tumors, called myxomas, from his heart. He is being considered for a heart transplant, but the transplant team needed a solid diagnosis to move forward.

Using long-read technology from Menlo Park, CA-based Pacific Biosciences, the Stanford team discovered a deletion of more than 2,000 base pairs in Ramons genome, confirming a diagnosis of Carney complex.

While short-read sequencing now costs less than $1,000 per genome, Ashley estimates the cost of the long-read sequencing used in this study to be between $5,000 to $6,000.

If we can get the cost of long-read sequencing down to where its accessible for everyone, I think it will be very useful, he said.

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DNA discovery reveals genetic history of ancient Egyptians – CNN

Posted: at 5:49 am

Researchers from the University of Tuebingen and the Max Planck Institute for the Science of Human History in Jena, both in Germany, have decoded the genome of ancient Egyptians for the first time, with unexpected results.

Modern Egyptians, by comparison, share much more DNA with sub-Saharan populations.

The findings have turned years of theory on its head, causing Egyptologists to re-evaluate the region's history while unlocking new tools for scientists working in the field.

Extracting genome data is a new frontier for Egyptologists, however.

Scientists took 166 bone samples from 151 mummies, dating from approximately 1400 B.C. to A.D. 400, extracting DNA from 90 individuals and mapping the full genome in three cases.

Previous DNA analysis of mummies has been treated with a necessary dose of skepticism, explains professor Johannes Krause of the Max Planck Institute.

"When you touch a bone, you probably leave more DNA on the bone than is inside (it)," he argued. "Contamination is a big issue. ... Only in the last five or six years has it become possible to actually study DNA from ancient humans, because we can now show whether DNA is ancient or not by (its) chemical properties."

Heat and high humidity in tombs, paired with some of the chemicals involved in mummification, all contribute to DNA degradation, the paper adds, but it describes its findings as "the first reliable data set obtained from ancient Egyptians."

Analyzing samples spanning over a millennium, researchers looked for genetic differences compared with Egyptians today. They found that the sample set showed a strong connection with a cluster of ancient non-African populations based east of the Mediterranean Sea.

Krause describes the far-reaching data set gained from looking at mitochondrial genomes: "This is not just the DNA of one person. It's the DNA of the parents, grandparents, grandparents' parents, grand-grand-grandparents' parents and so forth.

"So if we don't find sub-Saharan African ancestry in those people, that is pretty representative, at least for Middle Egypt."

Krause hypothesizes that ancient Northern Egypt would be much the same, if not more, linked to the Near East. Ancient Southern Egypt might be a different matter, however, where populations lived closer to Nubia, home of the "Black Pharaohs" in what is now Sudan.

"The genetics of the Abusir el-Meleq community did not undergo any major shifts during the 1,300-year timespan we studied," said Wolfgang Haak, group leader at the Max Planck Institute.

This period covered the rule of Alexander the Great (332-323 B.C.), the Ptolemaic dynasty (323-30 B.C.) and part of Roman rule (30 B.C.-A.D. 641). Strict social structures and legal incentives to marry along ethnic lines within these communities may have played a part in the Egyptians' genetic stasis, the paper speculates.

"A lot of people has assumed foreign invaders ... brought a lot of genetic ancestry into the region," Krause said. "People expected that through time, Egypt would become more European, but we see the exact opposite."

Modern Egyptians were found to "inherit 8% more ancestry from African ancestors" than the mummies studied. The paper cites increased mobility along the Nile, increased long-distance commerce and the era of the trans-Saharan slave trade as potential reasons why.

The team's findings do come with one obvious caveat: "All our genetic data (was) obtained from a single site in Middle Egypt and may not be representative for all of ancient Egypt," the paper concedes.

While the study might be limited in scope, the team believes it has made some technical breakthroughs.

"I expect there will be a ton of ancient Egyptian mummy genomes (mapped) in the next couple of years," Krause said, adding that "multiple groups" are following his team's lead.

"There's always more research we can do. This is not the end. It's just the beginning."

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Shaking Up Genome Regulation by Considering Oil/Water-Like … – Genetic Engineering & Biotechnology News

Posted: at 5:49 am

In the mixed-up world of gene silencing, its not exactly clear why some genomic regions are hard to access. These regions, it has been suggested, may simply be too tightly packed to permit the passage of regulatory proteins needed for functions such as DNA repair. Tightly packed DNA, however, doesnt always behave as expected. For example, heterochromatin has been known to exclude small proteins while admitting large ones.

Such anomalous behavior naturally attracts the attention of scientists. Eager to resolve the problems accompanying the compaction explanation for the silencing of heterochromatin, scientists based at Lawrence Berkeley National Laboratory decided to consider an alternative mechanism. It turns out to be the same one that accounts for the separation of oil and water.

A Berkeley Lab team led by Gary Karpen, a senior scientist specializing in biological systems and engineering, uncovered evidence that heterochromatin organizes large parts of the genome into specific regions of the nucleus using liquid-liquid phase separation, a mechanism well-known in physics but whose importance for biology has only recently been revealed.

Details appeared June 21, 2017 in the journal Nature, in an article entitled, Phase separation drives heterochromatin domain formation. The article suggests that phase separation, a phenomenon already known to have biological relevance in giving rise to diverse non-membrane-bound nuclear, cytoplasmic, and extracellular compartments, also mediates the formation of heterochromatin domains.

We show that Drosophila HP1a protein undergoes liquidliquid demixing in vitro, and nucleates into foci that display liquid properties during the first stages of heterochromatin domain formation in early Drosophila embryos, wrote the articles authors. Furthermore, in both Drosophila and mammalian cells, heterochromatin domains exhibit dynamics that are characteristic of liquid-phase separation, including sensitivity to the disruption of weak hydrophobic interactions, and reduced diffusion, increased coordinated movement, and inert probe exclusion at the domain boundary.

Essentially, the researchers observed two non-mixing liquids in the cell nucleus: one that contained expressed genes, and one that contained silenced heterochromatin. They found that heterochromatic droplets fused together just like two drops of oil surrounded by water.

In lab experiments, researchers purified heterochromatin protein 1a (HP1a), a main component of heterochromatin, and saw that this single component was able to recreate what they saw in the nucleus by forming liquid droplets.

Chromatin organization by phase separation, noted Amy Strom, study lead author and a graduate student in Karpen's lab, means that proteins are targeted to one liquid or the other based not on size, but on other physical traits, like charge, flexibility, and interaction partners."

The authors of the Nature article concluded that the heterochromatic domains form via phase separation mature into structures that include liquid and stable compartments. They also proposed that emergent biophysical properties associated with phase-separated systems are critical to understanding the unusual behaviors of heterochromatin, and how chromatin domains in general regulate essential nuclear functions.

"The importance of DNA sequences in health and disease has been clear for decades, but we only recently have come to realize that the organization of sections of DNA into different physical domains or compartments inside the nucleus is critical to promote distinct genome functions," commented Dr. Karpen.

The Berkeley Lab study, which used fruit fly and mouse cells, will be published alongside a companion paper in Nature led by UC San Francisco researchers, who showed that the human version of the HP1a protein has the same liquid droplet properties, suggesting that similar principles hold for human heterochromatin.

Interestingly, this type of liquid-liquid phase separation is very sensitive to changes in temperature, protein concentration, and pH levels.

"It's an elegant way for the cell to be able to manipulate gene expression of many sequences at once," commented Strom.

Other cellular structures, including some involved in disease, are also organized by phase separation.

"Problems with phase separation have been linked to diseases such as dementia and certain neurodegenerative disorders," remarked Dr. Karpen.

He noted that as we age, biological molecules lose their liquid state and become more solid, accumulating damage along the way. Dr. Karpen pointed to diseases like Alzheimer's and Huntington's, in which proteins misfold and aggregate, becoming less liquid and more solid over time.

"If we can better understand what causes aggregation, and how to keep things more liquid, we might have a chance to combat these types of disease," Strom suggested.

The work is a big step forward for understanding how DNA functions, but could also help researchers improve their ability to manipulate genes.

"Gene therapy, or any treatment that relies on tight regulation of gene expression, could be improved by precisely targeting molecules to the right place in the nucleus," explained Karpen. "It is very difficult to target genes located in heterochromatin, but this understanding of the properties linked to phase separation and liquid behaviors could help change that and open up a third of the genome that we couldn't get to before."

This includes targeting gene-editing technologies like CRISPR, which has recently opened up new doors for precise genome manipulation and gene therapy.

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The power of a billion: India’s genomics revolution – BBC News – BBC News

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The power of a billion: India's genomics revolution - BBC News
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Could an effort to gather genetic data from its population of one billion people help India take the lead in advanced healthcare?

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Cat Zingano says ‘hell yes’ to fighting winner of Cris Cyborg vs … – Bloody Elbow

Posted: at 5:48 am

She may be out of commission for a bit, but that doesnt mean shes not sharpening her knives. Former bantamweight title challenger Cat Zingano is still recovering from an undisclosed injury. But, despite not having fought since her decision loss to Julianna Pena at UFC 200, she been staying in the gym at Alliance MMA in San Diego and paying close attention to the rest of the division.

After Holly Holms sensational knockout win over Bethe Correia at UFC Singapore last weekend, Zingano had some thoughts about what she wants upon her return. Not only does she want a fight against Holm, but shes more than willing to take on the winner of the upcoming fight between Cristiane Justino vs Megan Anderson at UFC 214, if given the opportunity.

She discussed her intentions with Ariel Helwani over at MMAFighting.

Recently, I was asked about fighting her and for it to be in contention of possibly fighting the winner of Cyborg (Justino) vs. (Megan) Anderson. My answer is hell yes. As soon as my body is ready to safely go back in there, the heads will be rolling once again. The results and trials of the treatments Im focusing on are responding and that makes me happy to hear as an athlete, as well as a normal human. Longevity in health and sport are both my top priorities, as well as in the interest of the UFC, who is providing me huge support at this time.

Again, there are no details as to Zinganos condition or potential recovery time, so theres no way to predict how soon she can be back in action. She remains 9-2 in her professional career. Her UFC record currently stands at 2-2, however, after back to back losses to former champion Ronda Rousey and Julianna Pea. But, given the state of both the featherweight and bantamweight divisions right now, shes likely still in consideration as a top contender for match-ups with the divisional elite.

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