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Exploring an abandoned Soviet space station in Outreach – PC Gamer
Posted: July 18, 2017 at 3:48 am
You, a lone Soviet cosmonaut, are sent to investigate a communications blackout on a space station. When you arrive the place is falling apart, the crew is missing, and its up to you to find out what happened to the station and the workers aboard it. Set in the 80s, Outreach fuses real-world history with conspiracy theories. The environments are realistic, modeled on Russias famous Mir space station, meaning theres no technology that didnt exist at the time. Developer Pixel Spill spent months researching the era, and it shows. Everything from computer consoles to clothing has a feel of authenticity. Its like stepping back in time.
And this realism extends to the way you navigate the station, with zero gravity to deal with. You can push against scenery to propel your body forward, or grab railings to pull yourself along. Its slightly headspinning at first, and adjusting to the fact that theres no up or down takes some getting used to. But when you master it, floating around is a lot of fun. And when you realise that you can grab objects, throw them, and watch them spin through the air realistically, the story will take a temporary backseat as you experiment and play around with the physics. The zero-gravity movement feels just right, which is the result of a lot of painstaking tweaking and adjusting by Pixel Spill.
Theres something wonderfully eerie about the lifeless station. Abandoned space stations are nothing new in games, but the realism element in Outreach makes it feel unique. The chunky tech is reminiscent of Alien: Isolation, which Pixel Spill cites as a big influence on the art design. I drift through the station discovering remnants of the mysteriously missing crew: conversations recorded on cassette tapes, letters, and family photos. I methodically check each and every module for clues, but find nothing. Then I reach a door with a broken handle, meaning Im going to have to go for a spacewalk to reach the next area.
When I step outside into the expanse of space, the size of the Earth below makes me feel dizzy. The sense of scale is incredible. And while I felt relatively safe in the confines of the station, out here Im suddenly overwhelmed by dread. A sensation thats justified when I try and leap towards a handrail, only to miss, float helplessly away and die horribly in the depths of space.
This section is remarkably tense, requiring patience, timing, and concentration to carefully grab each rail and pull yourself to a distant airlock. You have to hit the grab button at precisely the right time, otherwise youll overshoot the rail and drift away from the station with no way to make your way back. I make it eventually, but I die several times in the process. Then, cruelly, the demo ends, and I dont get to see whats inside.
Outreach is fascinating, but my demo leaves me none the wiser about what kind of story itll tell. Will it be a psychological thriller? Or is there something supernatural going on aboard the station? Im looking forward to finding out in the finished game. Pixel Spill promises players will discover the lives and motivations of the crew and learn about something called Project Outreach, which sounds suitably sinister.
The developer also says that youll uncover the true nature of the space station as you explore it, which is filling my head with questions. Im told the game will be a relatively short experiencemaybe three or four hours, the length of a long movieand Im okay with that. Short, focused, well-told stories are fast becoming one of my favourite kinds of game on PC, and I hope Outreach is one that delivers
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NASA Offers Space Station as Catalyst for Discovery in Washington – Space Daily
Posted: at 3:48 am
NASA astronauts, scientists and engineers will join industry and academia for a three-day, in-depth conversation about the International Space Station (ISS) as a catalyst for discovery during the sixth annual ISS Research and Development Conference July 17-20 in Washington. Acting NASA Administrator Robert Lightfoot will provide the morning keynote on Wednesday, July 19.
See the conference agenda for a full list of topics and speakers. Keynote addresses and panels from the conference will be broadcast on NASA TV and the agency's website.
The conference, hosted by the American Astronautical Society and the Center for the Advancement of Science in Space (CASIS), in cooperation with NASA, brings together leaders from industry, academia and government.
Attendees will explore innovations and breakthroughs in microgravity research; life sciences; materials development; technology development; human health and remote sensing; the potential applications for space-based research; and the economic benefits of increased commercial activity in low-Earth orbit.
NASA astronaut Kate Rubins, who tested an innovative technology in orbit that may improve medical diagnoses in space and on Earth, will provide a keynote presentation. Rubins completed her first spaceflight in 2016, and was the first person to sequence DNA in space.
The technology she used could help diagnose potentially fatal diseases in remote locations, including during long space voyages. Rubins also grew heart cells in orbit, performing real-time analysis and experiments.
NASA and CASIS, both manage and fund research on the space station, will provide overviews of research applications, external and internal capabilities, and upcoming opportunities.
During the Monday, July 17 preconference day, NASA and the Japan Aerospace Exploration Agency (JAXA) will host a joint workshop covering the achievements and opportunities tied to cooperative use of unique JAXA experiment hardware for joint research.
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NASA Offers Space Station as Catalyst for Discovery in Washington - Space Daily
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Titan’s Alien Lakes Might Be Perfect Landing Spots for Colonization … – Outer Places
Posted: at 3:47 am
Titan, Saturn's largest Moon, has the potential to be an ideal location forhuman colonization and explorationwithin our Solar System, along withMars (though Mars' prospects have gotten less rosy lately). Some even arguethat,besidesEarth, it is theonly place suitable for human colonization in our celestial neighborhood. While it is unbelievably cold, distant, and strange, it is also home tolarge bodies of surface liquid, solid ground, a thick atmosphere, and more. And, to add to that list,scientists recently discoveredcalm hydrocarbon lakesthat could make landing future probes a piece of cake.
The highest that waves reach on the lakes of Titan is about one centimeter.These alien lakesare more tranquil than we might be able to picture, sitting remarkably still. And so, if and when we are able to send probes to that Moon, scientists think that these lakes would make a good landing point. According to lead author Cyril Grima, a research associate at the University of Texas Institute for Geophysics (UTIG): "There's a lot of interest in one day sending probes to the lakes, and when that's done, you want to have a safe landing, and you don't want a lot of wind...Our study shows that because the waves aren't very high, the winds are likely low."
Image Credit: NASA
So what does this mean? It might not sound that exciting at first glance, but it is a huge step forward in our never-ending cosmic exploration. Especially with the recent news that Mars' soilcould be toxic to any potential bacterial life, it is important to remember that the Red Planet isn't the only possible destination for future astronauts and probes. Titan could be the future location of a permanent human colony and the ability of a probe to successfully and smoothly land is crucial to missions going well. So, while we still have a long way to go (literally and more figuratively), this is one huge step in the right direction.
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Background on biotechnology Bill – New Vision
Posted: at 3:47 am
'Background on the National Biotechnology and Biosafety Bill'
Prof. Morris Ogenga-Latigo
1. Introduction
The National Biotechnology and Biosafety Bill 2012 is now before the 10th Parliament for consideration and enactment. This is a highly technical Bill that for long has endured relentless highly emotive campaigns against Biotechnology and Genetically Modified Organisms (GMOs).
To enable Members appreciate the context, purpose and content of the Bill, and debate and enact the law on the basis of clarity and objective information, I have prepared this scientific background information that frames and contextualizes the Bill.
I have done this not because some foreign entity is paying me to enact the law as some claim about MPs. HELL NO! Those who know Prof. Latigo well know that this can never be the case. I am doing this because this Bill is necessitated by the needs of our country that we as Parliamentarians are obligated under the Constitution to address by enacting appropriate laws.
More importantly, I saw the potential of Molecular Biology as long ago as the late-1980s when I was winding up my Ph.D. studies at the International Centre for Insect Physiology and Ecology (ICIPE), Nairobi. In 1996, as an Academic in Makerere University, I became the Focal Point on Biotechnology and a Founding Member of the National Biosafety Committee of the National Council for Science and Technology. I served the Council for 10 years (part of it when I was an MP in the 7th Parliament), and only resigned in 2006 when I became the Leader of Opposition.
In the 10 years, we supported Biotechnology capacity development for Uganda through graduate training and supporting establishment of dedicated Biotech Laboratories. With progress, we developed the National Biotechnology Policy and early drafts of the National Biotechnology and Biosafety Bill.
I am therefore deeply obligated to the country to inform and enlighten Members, and to do whatever I can to ensure that this Bill is passed into law to serve the best interest of our Country, our farmers, and agriculture that I love and am so deeply involved in.
In doing so, I act as a patriotic Ugandan of known academic, research and political leadership trek record and deep conviction, and one keen to share his little knowledge on crop improvement, Biotechnology and GMOs with colleagues, and never because of having been remotely corrupted or bribed by anybody.
My specific views on the Bill, on the Main and Minority Reports from the Committee, and on the proposed amendments of the various clauses of the Bill will be shared with you during the Second and Third Readings of the Bill. Below is a presentation on the genesis of the Bill.
2. Genetic Engineering, Biotechnology and the March of Science
Biotechnology is an applied science that derives from the core field of Biology, and the core subject of Genetics, both of which have developed over time and in complexity, and have become highly specialized and sometimes difficult to appreciate in the context of our cultures, religious beliefs, and our day to day life experiences.
From being the study of living organisms in their wholesome, Biology has now developed to the molecular level, hence the field of Molecular Biology. Similarly, from the study of inheritance and inherited physical variations in organisms, Genetics has moved to the levels of chromosomes, DNAs, genes, RNAs etc. and their manipulation, and out of which progress has emerged the science of Genomics.
Biotechnology applies these advanced knowledge and capabilities to generate modified life forms and their products in ways that transcend the ordinary boundaries of nature and the ordinary limits of natural processes.
Thus, in agriculture, whereas traditional Biology talks about species barriers in the inability to share genes amongst organisms that do not interbreed, Biotechnology allows us to move desired genes from one species to another regardless of natures sexual barriers. This has enabled us to exploit genes that exist in nature, and created by God as the building blocks of life, without the limits inherent in traditional methods of crop improvement.
Beyond Biotechnology, the science of Synthetic Biology and its applied field of Bio-hacking are also now emerging where, rather than genetically modifying crops or animals to do the things we want, we now use knowledge to imitate nature. Thus, amazingly, we are now able to produce milk without cows or beef without cattle.
3. Progress in Crop Improvement and the Imperative of Biotechnology
In the beginning, man relied on natural gene changes (mutations) to generate plant variations and diversity that he exploited by chance and choice, and refinement through repeated selection. With the advent of Genetics, we were able to deliberately cross plants of the same species to create variants and to then select for use those plants with attributes we most desired. This was the advent of conventional breeding.
More recently, rather than waiting for nature to modify genes and create plant variants for us to select from, radioactivity allowed us to imitate this natural gene change process. Using radioactive substances, we have been able to deliberately induce gene changes (mutations) and to then select mutant plants that best suit our needs that we then cross with other desired plants of the same crop in conventional breeding processes. This approach to crop improvement became known as Mutation Breeding.
Building on these sexual reproduction approaches to develop new crop types, the study of genetics later showed us that when you crossed plants of the same species from two lines of a crop that have distinct and stable attributes, their off-springs were more vigorous and had positive attributes greater than the additive value of the attributes of the two parent lines. This was the phenomenon of hybrid vigour, also seen in our half-caste children being physically much more vigorous in growth, size and activity than their two parents.
Breeders then began to develop pure crop lines of maize etc. that, when crossed, produced hybrids with superior performances. So emerged hybridization as a crop breeding technique the products of which are the hybrid crop varieties that yield far more than varieties developed using conventional breeding.
Hybridization and hybrid vigour have so far capped plant performance improvements. Nevertheless, hybrid breeding has been improved beyond the two pure line crosses. Now, we enhance performances and plant characteristics through double or multiline hybridization where two pure lines are crossed and the products of their crosses are further crossed to produce double or multi-line hybrids.
In all the above crop improvement approaches, there is always one natural barrier to the sharing of genes between different crops to produce desirable characteristics. In nature, a desirable gene in species A cannot be moved to species B because of the species barrier rule that says that one crop species cannot breed with another crop species.
Thus, whereas one maize type can cross with another maize type, maize will never cross with cotton. If a cotton line is resistant to a plant disease X, therefore, using conventional breeding, the cotton can be crossed with another cotton line that has good characteristics but is attacked by disease X. Through repeated crossing and screening, a cotton line will eventually be developed that will possess both the good characteristics and resistance to disease X. This then becomes the new disease resistant cotton variety.
Even when the disease X attacks both cotton and maize, as often happens, however, the resistance to disease X identified in cotton cannot be transferred to maize through conventional breeding because of the cross-species reproductive barrier.
In the quest to break this species barrier so that the disease resistance in cotton can be shared with maize and other crops, scientists developed techniques for transferring desirable genes across species using their understanding of molecular biology, genomics, and biochemistry. The techniques so developed became known as Genetic Engineering, and the science that encompasses the whole process became known as Biotechnology.
4. Enter Monsanto and GMO crops
Monsanto was the company that developed the herbicide glyphosate, which in the sixties and seventies was marketed in Uganda as Roundup and was extensively used to control weeds in coffee and banana fields. In the various advocacies against Biotechnology and GMOs, this company and its products are the demons used to scare us off.
Glyphosate is a general purpose insecticide that is basically less poisonous to man than a strong drink of caffeine of coffee. It is not a poison to us because we do not have cell receptors on which it must attach in order to react with and kill our body cells. Thus, when we swallow or absorb glyphosate, our kidneys merely filter it out and is mostly excreted unchanged in urine.
In weeds, however, glyphosate is absorbed by leaves and transported to roots. There, it binds with a single enzyme and disrupts root metabolism. The root then dies stopping the plant from taking up water and nutrients, and the plant is gradually starved to death. This explains why when we apply glyphosate today weeds remain green for days before turning yellow and only drying up after 2-3 weeks.
As glyphosate became widely used, it was noticed that certain plants did not die even when the glyphosate dose used was high. Monsanto scientists, in studying this phenomenon to overcome the limitations of their product, identified these plants as having ability to break down glyphosate and render it harmless to the resistant plants.
From their study to understand why their herbicide did not work, the Monsanto scientists saw an opportunity of transferring this herbicide resistance attribute from weeds to crop plants, such that now plants with the resistance attribute can be grown with weeds and glyphosate is then used to eliminate the weeds but will not kill the modified crops.
Monsanto identified and isolated the gene that was responsible for producing the enzyme that broke down glyphosate once it was sprayed on the resistant weed and introduced it in crop plants (maize, soybean). To protect its commercial interest, Monsanto patented the gene and the process of its transfer into crops.
Using genetic engineering, they transferred this gene into maize, and later soybean, and developed their own commercial GMO maize and soybean varieties that could be grown with weeds but that would not be killed when glyphosate is applied to kill weeds growing with them. This is the genesis of the controversies about GMOs, Monsanto, and the supposed dominance of Biotechnology, genetic engineering and seed supply by multinational corporations.
Because of the gene patent restriction secured by Monsanto, the only option left to fight Monsanto was to demonize Biotechnology, the products of genetic engineering, and the companys GMO crop varieties. Hence the claims of: the evil of foreign genes, the carcinogenicity of glyphosate or Monsantos GMO maize, the sinister plans of multinationals to deprive us of our indigenous seeds and food sources etc. The truth however is far from this.
5. The Controversies Surrounding Biotechnology and GMOs
There have been numerous attempts to scare us off Biotechnology and its GMO crops and products, through arousing uncertainty and deep fear of the unknown. The scare-mongering is, however, essentially unjustified and is absolutely unjustifiable in science, facts and realities.
Firstly, there is no gene that is foreign. The mould for the bricks used to construct all living things is the gene. The traits of a human being, for example, are based on the expression of approximately 80,000 genes packaged in structures called DNAs. The genes that are inherited from our parents contain all the biological instructions (moulds for making the bricks) for building a human being.
Just as each unique brick mould will produce a unique brick, every gene in the DNA codes (instructs) the making of only one unique protein (enzyme) needed in our biological processes. Whether that brick is used to build a latrine, a residential house etc. does not matter because, wherever it is, the brick will do precisely what it is supposed to do only, and can never become cement or paint.
Similarly, a gene will encode for only that one protein required to fulfill a particular function in the building of a living organism, be it a bacterium, maize, banana or us humans, and we share many such genes. In fact, around 96% of the genes in us humans are shared with chimpanzees and mice, and we humans share approximately 99% of our DNA with other humans, 98% with chimps, 70% with slugs and 50% with bananas.
So where does the distinction and the fear of foreign genes or DNAs and their harmful effects when a gene from another source is inserted into a crop come from, particularly when the genes involved in GMO crops are even from other plants?
If that one gene that codes only the making of that one enzyme that breaks down glyphosate and nothing else is inserted into a maize variety so that the maize becomes resistant to glyphosate, where do the claims of harmfulness or risks of it causing cancer then come from? So what is the fear of Biotechnology and GMOs based on, and why the extreme caution about GMOs?
Secondly, whether in conventional breeding, mutation breeding, hybridization, genetic engineering or even human reproduction, new characters are only produced because the original genetic compositions of the source parents have been modified. In other words, every life form that is different in character and other attributes from any of the parents, as we all are different, is essentially and truthfully a genetically modified organism or GMO.
The only difference now is that crops modified through the process of genetic engineering or Biotechnology are called GMOs, and are feared and demonized, whereas all the other crops that are also genetically modified using conventional breeding methods, are now called non-GMOs, are not feared or demonized, and are easily accepted.
Thirdly, we can never take control of Biotechnology and use it to define our future and utilize it to address our challenges and fulfill our needs unless we build our internal capacities and take charge of the science and the opportunities it offers us, our competitors and the world.
China did not counter the threats and dominance of nuclear USA or Russia by propagating the fear of Nuclear Science. Instead they built their capacities in Nuclear Science and relevant technologies, and ability to exploit the potentials embedded in the science. And now they are part of the worlds Nuclear Powers, with the USA and Russia, and respected by the two countries.
Fourthly, as Ugandans, the threat to our key crops, Coffee and Bananas, by the emergence of new diseases (bacterial wilt etc.) offers us the best opportunity to appreciate the value of Biotechnology and genetic engineering to the security of our country and people.
Bacterial wilts have devastated our coffee and banana crops because the varieties we grow do not possess resistance to these diseases. For coffee, if we are to develop new resistant varieties through conventional breeding, it means we have to first identify coffee plants resistant to the wilt, and grow them and cross them with our commercial varieties. We then have to test thousands of their off-springs to identify plants with resistance to the wilt, and also grow the resistant plants to determine whether they have the same commercial attributes of our susceptible varieties.
Where the identified resistant lines do not meet our standards, we have to undertake repeated backcrossing with the susceptible parent and repeated selection until we get the desirable varieties resistant to the disease for release to farmers.
Since the maturity period for coffee is at least 4-6 years, this conventional breeding approach will require 20-30 years for us to develop new coffee varieties resistant to the wilt. In these 20-30 years, what would happen to our coffee industry, to the livelihoods of our farmers, and to the economy of our country?
The challenge is even worst for our bananas that do not reproduce sexually, and are only propagated vegetatively. Thus, even if we identify a local banana line resistant to bacterial wilt, it is not possible to transfer that resistance to the other susceptible banana varieties through conventional breeding because our bananas do not breed or cross in nature sexually.
Thus, for our bananas and coffee, that multinationals have little interested in, our only means to protecting them against emerging diseases, pests and the challenges of climate change, or to quickly improving them to meet our needs, is to develop our national capacity to identify sources of resistance and other desirable genes and to be able to quickly move these genes within the pool of our coffee and banana varieties through Biotechnology and genetic engineering.
If we reject Biotechnology because some people have demonized it and GMOs, what options do we have for our country?
6. Final Appeal
Here in Uganda, since the late-1990s, we recognized the potential of Biotechnology and embarked on building our capacities (human resources and labs) to exploit this potential for rapid crop varietal development in light of emerging new diseases and pests, the effects of climate change and drought, and the need to produce enough food of the right qualities to meet our needs now made urgent by our rapid population growth.
Consequently, we have built a large body of highly competent and internationally recognized scientists who are working diligently, honestly and selflessly in our ultramodern Biotechnology Laboratories at Makerere University, Kawanda, Namulonge etc., but who are being held back by the absence of a legal regime to enable them work without fear of potential undefined liabilities.
The operational framework to enable our scientists engage in Biotechnology capacity development and its exploitation, in conformity with international standards and protocols, is this National Biotechnology and Biosafety Bill that meets the international standards set out in the Convention on Biodiversity (CBD) and the Cartagena Protocol on Biosafety (CPB).
The National Biotechnology and Biosafety Bill 2012, now before Parliament, is a draft law formulated by us as a country to enable us safely develop our Biotechnology capabilities in order to secure our future and wean and protect us from potential dependence on, and bondage of, multinational interests.
This aspiration will never be achieved: When we are driven to legislate out of propaganda and fear, and out of unfounded suspicion that the Bill that was developed and introduced by the Government of the ruling NRM Party is actually a Bill pushed by multinationals to meet their selfish interests. When our scientists, whom we invested in and are working in the field of Biotechnology, are demonized, maligned and presented in bad light, and their voices ignored, and when the falsehoods propagated by CSOs and some non-Biotech scientists about the dangers of Biotechnology and GMOs are instead believed and are the basis of our legislative drive. And when our individual biases- religious, political, ideological etc.- take precedence over our obligation to legislate in the best interest of our country.
Against the above, I make a passionate appeal to us all, Members of the 10th Parliament, individually and collectively, to accept the facts of Biotechnology and our National aspirations to exploit its potentials as the sole basis for inputting into the process of considering the National Biotechnology and Biosafety Bill 2012 now before us, and to trust in the expert advice that our scientists and some of us, your colleagues, are able to offer to the August House.
Please let us take our obligation to act as Patriots and to legislate non-emotively, and in the best interest of our country and people, most seriously.
The writer is the MP for Agago North, Member of the Pan African Parliament and the former Leader of Opposition in 8th Parliament. He is also the former member of the Uganda National Biosafety Committee (1996-2006)
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Background on biotechnology Bill - New Vision
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Chinese scientists who made muscly ‘super dog’ could create genetically-modified human CHILDREN next’ – The Sun
Posted: at 3:47 am
China's Dr Frankensteins are 'on a path to eugenics' as they tinker with the genetic code of animals - and we could be next
CHINESE scientists who are cloning canines to create mutated superdogs are on the road to eugenics, a top genetics expert has warned.
The pups, like the one below, are being bred to become stronger and faster and could be used for security or policing.
Sino Gene
Experts at Sino Gene, a biotech company based in Beijing recently revealed afluffy beagle called Long Long to the world.
It is the first of his kind because it has been cloned from a genetically modified parent, they claimed.
The pup arrived in late May in a Sino Gene lab, exactly where her dad was born in December last year.
But despite its adorable appearance, a British genetics expert said he is very concerned about how the scientists are using genetics for non-medical purposes.
Scientists genetically modify animals in the UK to test medicines like cancer treatments on mice, rabbits or dogs.
David King, director of Human Genetics Alert (HGA), warned that this was the first step to creating mutant children.
Asia Wire
Its true that the more and more animals that are genetically engineered using these techniques bring us closer to the possibility of genetic engineering of humans.
Dogs as a species, in respect of cloning, are very difficult and even more difficult to clone human beings.
Theres no medical case for it, the scientists are interested in being the first person in the world to create a genetically-engineered child.
Theyre interested in science and the technology and their careers. They will continue pushing the regulations for it.
Asia Wire
Eyevine
That does set us on the road to eugenics. I am very concerned with what Im seeing, he told the Express.co.uk.
Lai Liangxue, a researcher at the Guangzhou Institute of biological medicine and health, told China Plusthat the birth of Long Long put China on the map.
He said: This is a breakthrough, marking China as only the second country in the world to independently master dog-somatic clone technology, after South Korea.
With this technology, by selecting a certain gene of the dog, we can breed an animal with more muscles, a better sense of smell and stronger running ability, which is good for hunting and police applications.
Liangxue has already created the worlds first gene-edited dogs. beagles named Hercules and Tiangou.
They double the amount of muscle mass of a typical dog of its breed by deleting a gene called myostatin.
The dogs have more muscles and are expected to have stronger runningability,which is good for hunting, police (military) applications, Liangxue told MIT review back in 2015.
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Chinese scientists who made muscly 'super dog' could create genetically-modified human CHILDREN next' - The Sun
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Searching for an answer in DNA – WBIR-TV
Posted: at 3:46 am
Family tales and photos reveal only part of our ancestral story. A clearer picture of our past and even our future lies deeper - in our genes. That's why WBIR Marketing Director Kara McFarland turned to science to fill in some blanks.
Robin Wilhoit, WBIR 8:10 PM. EDT July 17, 2017
WBIR Marketing Director Kara McFarland was adopted as an infant. She used the genetic testing kit23andMe" to learn more about her biological familys history. (Photo: WBIR)
Family tales and photos reveal only part of our ancestral story. A clearer picture of our past and even our future lies deeper in our genes. Thats why WBIR Marketing Director Kara McFarland turned to science to fill in some blanks.
Kara always knew she was adopted as a newborn. She never gave it a second thought that she looked nothing like her dark haired, olive skinned adoptive parents. But as she grew, so did her curiosity.
I went on a journey of discovery on my own. I didnt tell them, said Kara. "I was able to find in my basement the adoption file and I found some photos. One photo, I just couldnt believe it. It was like looking at my reflection.
A baby photo of Kara and her adoptive parents. Photo courtesy Kara McFarland. (Photo: WBIR)
Karas curiosity eventually turned into questions about her background and her health based on her biological familys history. Theyre questions that can now be answered with at-home genetic testing kits you can buy online. A simple saliva sample can reveal what part of the world you come from, who you are related to and potential health risks.
Kara used the genetic testing kit 23andMe. She spit into a small tube, answered some questions online, sealed up the kit and sent it off in the mail.
Four weeks later Karas genetic findings were in her computer inbox. It revealed she is 96.8% Northwestern European, among others.
There is British, Irish, a little French and German. It says 1% Scandinavian. A lot of people ask me if Im Scandinavian but I dont know anything about that. Im excited to learn," she said.
Kara's genetic findings from her 23andMe test. (Photo: WBIR)
The test also gives Kara heads up on variants in her genes that put her at risks of certain health conditions. It turns out, she has a slightly increased risk of developing late onset Alzheimers Disease.
The only thing you can do is do your research and practice a healthy lifestyle, said Kara.
Now armed with information, Kara has a glimpse into her future and a clearer picture of her past.
I still identify as Yugoslavian and American Indian. Thats what I was raised to know. Now I can research and learn a little bit more about those areas and feel a connection to a people I havent felt a connection to," she said.
Tuesday on 10News at 6, an expert will share how these test kits work and the accuracy of the findings.
2017 WBIR.COM
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On ‘LHH’ Finale & Fans Are Furious See Tweets – Hollywood Life
Posted: at 3:46 am
Love & Hip Hop fans who tuned in for the shows final reunion episode were in for a major let down, as Kirk Frost refused to reveal DNA test results that would prove if he had a lovechild a plot point the show had been building to ALL season.
Vh1 needs to listen up, because we have some really good advice: Do not disappointLove & Hip Hop: Atlantafans. They are a vicious, hilarious, savage crew who will come at you if you do not deliver on a promise. Thats exactly what happened on July 17, when LHHfans went into a rage afterKirk Frost, 48, refused to reveal DNA test results that would prove if he was the father of Jasmine Washingtons son during the seasons final reunion episode.The story of Kirks infidelity in his marriage to wife Rasheeda had been a MAJOR part of season 6 and fans wanted the return on their investment.
Viewers immediately went to the best place to vent their frustrations Twitter. There they wrote responses to this complete betrayal that were absolutely epic. WAIT. Sooo they focused the entire season on Kirks infidelity and we STILL dont know if the child is his!! Im done, one fan tweeted. Kirk still didnt take DNA on this d**n baby. He was so fast take a secret DNA test on Rasheedas son . FOH , another fan wrote. So we really not making Kirk do a paternity test. Like he aint made a WHOLE baby on Rasheeda?! another user tweeted, defending Kirks wife of almost 20 years. The only thing better than the tweets were the GIFs that accompanied them.
Jasmine did not participate in the reunion special and actually made some social media noise of her own when the first part aired last week. Kirks alleged baby mama took to Instagram to share alleged texts between herself and Kirk that show him being involved in his sons life and even telling her he loved her.
HollywoodLifers, do you think Kirk should have refused to take the test? Let us know below!
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How Much Should You Trust Your DNA Test? – Newsy
Posted: at 3:46 am
ByTyler Adkisson July 17, 2017
For thepast 10 yearsor so, direct-to-consumer genetic tests have made determining your ancestry and predisposition to some diseases as easy as mailing a cotton swab of spit to a lab. But how reliable are they?
In some cases, it's hard to say what counts as accurate because the science isn't very precise to begin with. Ethnicity isn't determined by a specific gene, so the results actually show users where similar DNA has been found around the globe.
And for the few companies that do show their math, like Ancestry.com, their sample sizes are relatively small. They divide the world into 26 genetic regions and use only 115 samples to determine what's representative of a specific region.
Other companies don't even publish how they get their results, making it hard to check their work. Each also relies on its ownunique algorithms, so consumers could get different results depending on the company they choose.
Related StoryWhat DNA Testing Can Tell You, From Serious To Silly
That's why many personal genome service kits include disclaimers, like "for recreational purposes."
Regulating the industry hasn't been easy, either. In 2013, the Food and Drug Administration sent 23andMe awarning letterfor failing to assure its product was "analytically or clinically validated" for diagnosing some diseases. It wasn't until 2017 when the company got some approval from the agency.
So, if you think you're in the market for a DNA test, theFDAandCenters for Disease Control and Preventionsuggest meeting with a doctor.
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At least 75 per cent of our DNA really is useless junk after all – New Scientist
Posted: at 3:46 am
Luckily, our children dont inherit too many dangerous mutations
Blend Images /ERproductions Ltd/Getty
By Michael Le Page
Youre far from a perfect product. The code that makes us is at least 75 per cent rubbish, according to a study that suggests most of our DNA really is junk after all.
After 20 years of biologists arguing that most of the human genome must have some kind of function, the study calculated that in fact the vast majority of our DNA has to be useless. It came to this conclusion by calculating that, because of the way evolution works, wed each have to have a million children, and almost all of them would need to die, if most of our DNA had a purpose.
But we each have just a few children on average, and our genetic health is mostly fine. The study therefore concludes that most of our DNA really must be junk a suggestion that contradicts controversial claims to the contrary from a group of prominent genomics researchers in 2012.
When researchers first worked out how DNA encodes the instructions for making proteins in the 1950s, they assumed that almost all DNA codes for proteins. However, by the 1970s, it was becoming clear that only a tiny proportion of a genome encodes functional proteins about 1 per cent in the case of us humans.
Biologists realised that some of the non-coding DNA might still have an important role, such as regulating the activity of the protein-coding genes. But around 90 per cent of our genome is still junk DNA, they suggested a term that first appeared in print in a 1972 article in New Scientist.
But throughout the 2000s, a number of studies purported to show that junk DNA was nothing of the sort, based on demonstrating that some tiny bits of non-coding DNA had some use or other. These claims proved popular with creationists, who were struggling to explain why an intelligently designed genome would consist mostly of rubbish.
The grandest claim came in 2012, when a consortium of genomics researchers called ENCODE declared that, according to their project, a huge 80 per cent of the DNA in the human genome has a function. They had spent $400 million, they wanted something big to say, says Dan Graur of the University of Houston.
Graur is one of many researchers who didnt believe ENCODEs claim. The heart of the issue is how you define functional. ENCODE defined DNA as such if it showed any biochemical activity, for instance, if it was copied into RNA. But Graur doesnt think a bit of activity like this is enough to prove DNA has a meaningful use. Instead, he argues that a sequence can only be described as functional if it has evolved to do something useful, and if a mutation disrupting it would have a harmful effect.
Mutations to DNA happen at random for several reasons, such as UV radiation or mistakes made when DNA replicates during cell division. These mutations change one base of DNA into another an A to a T, for example and when they occur in a gene are more likely to be harmful than beneficial.
When we reproduce, our children inherit a shuffled bag of mutations, and those with a collection of particularly bad ones are more likely to die before having children of their own. This is how evolution stops bad mutations building up to dangerously high levels in a species.
Following Graurs logic, if most of our DNA is functional, we would accumulate a large proportion of harmful mutations in important sequences. But if most of our DNA is junk, the majority of mutations would have no effect.
Graurs team have now calculated how many children a couple would need to conceive so evolution could weed out enough bad mutations from our genomes as fast as they arise. If the entire genome was functional, couples would need to have around 100 million children, and almost all would have to die. Even if just a quarter of the genome is functional, each couple would still have to have nearly four children on average, with only two surviving to adulthood, to prevent harmful mutations building up to dangerous levels.
Taking into account estimates of the mutation rate and average prehistorical reproduction rate, Graurs team calculated that only around 8 to 14 per cent of our DNA is likely to have a function.
This ties in nicely with a 2014 study that compared our genome with other species and concluded that around 8 per cent of it is functional.
The findings are entirely supportive of one another, says one of the authors of the 2014 study, Chris Ponting of the University of Edinburgh, UK. We are walking around with a genome where only 1 in 10 bases actually matters.
We dont know how much of our DNA has a non-sequence-related function, says Ryan Gregory of the University of Guelph in Canada. Some regions of DNA are useful without having an important sequence, so mutations in these areas probably dont matter. But even taking this into account, most DNA is probably junk, says Gregory.
The challenge for those who think most non-coding DNA is vital is to explain why an onion needs five times as much of it as we do, says Gregory. I would like to think that most knowledgeable biologists who properly appreciate evolutionary theory and genomic diversity are well aware of the many problems with ENCODEs claim, he says.
But most people and even some scientists are uncomfortable with the idea that most of their DNA is junk, says Ponting. Even worse for such people, other genomic studies are now revealing that we all carry plenty of mutations that affect both our coding DNA and non-coding DNA. While evolution weeds out some of the worst ones, this doesnt stop plenty of mutations collecting in our genome.
We are walking around as individuals with relatively large numbers of our genes not working properly, he says. These are ideas some find shocking.
Journal reference: Genome Biology and Evolution, DOI: 10.1093/gbe/evx121
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Longevity, education, and the huge new worldwide increases in equality – American Enterprise Institute
Posted: at 3:45 am
If we widen our gaze from income inequality, it should be almost immediately apparent that a number of remarkable worldwide trends that are not only improving the human condition overall, but also making that condition markedly less unequal.
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Is the human condition becoming more unequal? A chorus of authoritative voices today insists that the answer is yes, unquestionably so. Inequality, the voices say, is sharply on the upswing in America, as everyone is supposed to know. It is also on the rise throughout other affluent democracies, they inform. We further hear that growing worldwide inequality is all but foreordained by the global triumph of capitalism: in 2014s runaway international bestseller Capital in the 21st Century, Thomas Piketty even has a formula to prove it.
The trouble with todays received wisdom about growing inequality, though, is that it focuses almost exclusively on the matter of economic inequality, and usually more narrowly still on only income inequality. Although this distinction may sound unobjectionable, it is actually quite problematic in two key respects.
For one thing, our true ability to measure economic inequality remains far less precise than is generally understood. Even in data-rich America, for example, statistics on the nations wealth distribution are at best rudimentary. Estimates of economic inequality differ dramatically depending on whether one looks at personal income or instead examines personal consumption, which seems to be distributed much more evenly.
This excerpt is part of a chapter that appears inAnti-Piketty Capital for the 21stCentury, 2017 the Cato Institute. Used by permission. Copies are availablehere.
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