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Daily Archives: March 29, 2017
Identifying genes key to human memory: Insights from genetics and cognitive neuroscience – Science Daily
Posted: March 29, 2017 at 10:49 am
Identifying genes key to human memory: Insights from genetics and cognitive neuroscience Science Daily The study is among the first to identify correlations between gene data and brain activity during memory processing, providing a new window into human memory. It is part of the nascent but growing field of 'imaging genetics,' which aims to relate ... |
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New genetic disorder named for Children’s Hospital of Philadelphia … – Science Daily
Posted: at 10:49 am
New genetic disorder named for Children's Hospital of Philadelphia ... Science Daily Three scientists at Children's Hospital of Philadelphia who identified and studied a genetic disease have been recognized by having their names attached to the ... |
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Steve May: The future genetic ghetto – VTDigger – vtdigger.org
Posted: at 10:49 am
Editors note: This commentary is by Steve May, who is a member of the Richmond Selectboard and a licensed independent clinical social worker. He has served previously as a national director of state Affairs for the Hemophilia Federation of America and is founder of The Forum on Genetic Equity, a national organization on genetic bias.
H.R.1313 (the Preserving Employee Wellness Programs Act) passed markup out of the House Ways and Means Committee on a party line vote with 22 Republicans voting for the bill and 17 Democrats voting against it. While the bill hasnt gotten anywhere near the attention the repeal of the Affordable Care Act has, overturning genetic privacy rules would have every bit as consequential an impact. H.R.1313 would permit genetic testing to be rolled into workplace wellness programs.
Obama era laws and regulations permitted for certain workplace wellness programs to be voluntary. The degree by which it would be voluntary going forward serves as something of an open question. There is a consensus amongst hiring managers and HR professionals that the only programs which are truly effective are the ones which target costly chronic and genetic conditions. Employers in targeting these would gain two significant pieces of information. Through enrollment and utilization they could target those who are healthy and identify those who have reason to believe they are not.
People with genetic conditions will either not be hired or hired at lower wages than they otherwise would have received as their employers and thus their insurers now know with less uncertainty future medical expense obligations.
These programs through coercive activity or incentive would create an opt-in and present little concern for those who are well. They would present their own genotype eagerly, demonstrating their own genetic wellbeing. Even a voluntary system shifts the onus onto those who for one reason or another chooses to not participate. Second, though opting out these employers would get genetic profiles with highly probable high cost diseases flagged. Far more dangerous to workers would be ones decision to not participate. While voluntary, these programs intend to compel individual participation by employers. If the cost of non-participation is high, that is a very valuable signal that the non-participating person has a damn good reason to not participate. And now they have demonstrated that they are not a team player which is really a proxy for a high likelihood of having a high probability of having a high cost genetically influenced condition. So people with genetic conditions will either not be hired or hired at lower wages than they otherwise would have received as their employers and thus their insurers now know with less uncertainty future medical expense obligations.
Following more than a decade of consultation, lobbying and advocacy, a Democratic Congress passed and a Republican president enthusiastically supported, championed and signed the Genetic Information Non-discrimination Act (GINA) in 2008. GINA is widely considered to have been the first major civil rights law of our new century; and it has successfully managed to safeguard the genetic privacy rights of every American every day for the last decade. The American Society for Human Genetics has come out against the passage of H.R.1313 because it would effectively repeal the fundamental genetic and health privacy protections in GINA and the Americans with Disabilities Act. Passage of H.R.1313 would permit workplace wellness programs to ask employees questions about genetic tests taken by themselves or their families, and to make inquiries about the medical history of employees, their spouses, their children, and other family members as employees. It is foreseeable that hiring and promotion decisions could depend on the results of genetic testing.
Under existing law, an employer may not ask a potential employee to take a genetic test as a condition of employment. That is to say they cannot pit two roughly equal applicants against one another and then consider the genetic factors and future affliction that might affect eventual employment. Supposing that you might be a carrier for BRCA-1, the genetic marker associated with breast cancer and another candidate may not, that single factor alone may be determinative in whether you get a job or a future promotion. It must be pointed out that simply being a carrier for a genetic condition does not mean that one necessarily will experience onset in most cases. In spite of that fact however, hiring managers can make employment decisions based on potential future health care costs in choosing one candidate over another.
Perhaps even more concerning is the potential for the discovery of a genetic predisposition, like Huntingtons disease. For that individual, somebody who will almost definitely contract the medical condition much later in life, (but not for several decades) the prospect of genetic profiling is downright harrowing. Huntingtons or Parkinsons will present if detected on one genetic profile, but the discovery of its existence may not affect ones health and wellbeing when it is discovered on a healthy individuals profile removed by many decades from actual onset for a given individual. In this case, the intervening event impacting ones health may be completely different, and human resource professionals, hiring managers and employers are ill-equipped to make decisions about the complex science of genomics and therefore use a disclosure as the basis to preclude one from the employment pool. Equally distressing is the idea that health insurance companies would be permitted to use genetic information and big data to inform patterns of underwriting in health insurance.
In the absence of GINA, genetic profiling could be used to determine health insurance rates. Currently, nothing precludes insurance companies from using this data in underwriting life, long-term care and disability insurance as policy makers have historically trailed badly behind this emerging technology. We dont redline neighborhoods anymore, why would we permit the formation of virtual genetic ghettos? Using factors like: race, class, gender, socio-economic status to inform patterns of underwriting in insurance products is bad public policy, why would using genetic predispositions in the form of genotyping be any better?
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Gene Linked to Wide Range of Intellectual, Physical Disabilities – Technology Networks
Posted: at 10:49 am
An international team of researchers from institutions around the world, including Baylor College of Medicine, has discovered that mutations of the OTUD6B gene result in a spectrum of physical and intellectual deficits. This is the first time that this gene, whose functions are beginning to be explored, has been linked to a human disease. The study appears in the American Journal of Human Genetics.
Our interest in this gene began when we carried out whole exome sequencing the analysis of all the protein-coding genes of one of our patients who had not received a genetic diagnosis for his condition that includes a number of intellectual and physical disabilities, said co-first author Dr. Teresa Sim, a postdoctoral associate of molecular and human genetics and a fellow in Clinical Molecular Genetics and Genomics. We identified OTUD6B, a gene that until now had not been linked to a health condition.
We identified a presumed loss-of-function mutation in the OTUD6B gene in our first patient, said co-senior author Dr. Magdalena Walkiewicz, assistant professor of molecular and human genetics at Baylor and assistant laboratory director at Baylor Genetics. We discovered that this gene seemed to be highly involved in human development; when the gene cannot fulfill its function, the individual presents with severe intellectual disability, a brain that does not develop as expected and poor muscular tone that limits the ability to walk, as well as cardiovascular problems.
Making a convincing case for OTUD6B
However, one case does not represent sufficient evidence to support the involvement of OTUD6B in the medical condition.
To make a convincing case that this gene is essential for human development we needed to find more individuals carrying mutations in OTUD6B, Walkiewicz said.
Mutations in OTUD6B are rare so the researchers had to look into the exomes all the protein-coding genes of a large number of individuals to find others carrying mutations in this gene. Walkiewicz and her colleagues first looked into their clinical exome database at Baylor Genetics labs, specifically into the data of nearly 9,000 unrelated, mostly pediatric-age individuals, many of which carrying neurologic conditions, and found an additional individual carrying genetic changes in the same gene. The clinical characteristics of this individual were strikingly similar to those of the first patient, which led the team to expand their search for more patients.
When we study very rare disorders we rely on collaborations with scientists around the world to find other families affected by mutations in one gene, said Walkiewicz.
One of the strategies that helps researchers find more cases is running the gene of interest through GeneMatcher, a web-tool developed as part of the Baylor-Hopkins Center for Mendelian Genomics for rare disease researchers. Similar to online dating websites that match couples, GeneMatcher allows researchers to find others that are interested in the same genes they are working on.
Without this type of collaborations it would be very difficult to make a convincing case. Between GeneMatcher and our database we found a total of 12 individuals carrying mutations in OTUD6B and presenting with similar clinical characteristics, Walkiewicz said.
An animal model corroborates the human findings
Animal models are one way to determine whether a change in this gene is actually causing the condition, said co-senior author Dr. Jason Heaney, assistant professor of molecular and human genetics and director of the Mouse Embryonic Stem Cell Core at Baylor. Having a similar change in an animal model gene that results in similar characteristics in a mouse can show us whether the gene is causing the condition.
Baylor is part of the International Mouse Phenotyping Consortium. Its goal is to generate a knockout model for every gene in the mouse genome, about 20,000 protein-coding genes, and determine what each gene is involved with.
In this case we learned in the animal model lacking the OTUD6B gene that the gene is highly expressed in the brain and we knew that the patients had reduced intellectual capacities. The animals had cardiovascular defects very similar to those in the patient population. The animal models allowed us to see that having this mutation of this gene causes the clinical characteristics observed in the patients. It highlights how useful animal models can be for understanding human disease, Heaney said.
Through multiple lines of evidence the researchers have established that mutations in OTUD6B can cause a range of neurological and physical conditions and highlight the role of this gene in human development.
In addition, our collaborators in Germany performed functional analysis for this gene on blood cells from patients, Walkiewicz said. Their findings suggest that the OTUD6B protein contributes to the function of proteasomes, large molecular complexes that are at the center of the cellular process that degrades proteins that are damaged or are not needed by the cell. This discovery strengthens the notion that disturbances of the proteasome can cause human disease.
There is interest in better understanding the mechanisms of the disorder at the cellular and molecular level. By understanding the processes that lead to the disease, we can then hope to develop therapies for those patients, said Walkiewicz. One of the highlights of this project is the tremendous collaboration with a number of different centers and labs and putting this tremendous effort together resulted in a publication that is very strong.
Another important contribution of this project is that we provided some answers for the families, and brought them together which offers the opportunity of mutual support, said Sim.
This article has been republished frommaterialsprovided by Baylor College of Medicine. Note: material may have been edited for length and content. For further information, please contact the cited source.
Reference
Teresa Santiago-Sim, Lindsay C. Burrage, Frdric Ebstein, Mari J. Tokita, Marcus Miller et al. and Federico Zara. Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features. The American Journal of Human Genetics, 2017; DOI: 10.1016/j.ajhg.2017.03.001
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DNA Is Being Collected to Protect Sex Workers, But It Could Also Be Used Against Them – Gizmodo
Posted: at 10:48 am
Nearly a decade ago, Dallas police proposed a new program designed to get sex workers off the streets. Rather than just send them to jail, police would set up shop at truck stops, accompanied by counselors, social workers and nurses, and give the sex workers a choice of either prison or talking to a counselor. But the program also had a grimmer, more ethically fraught componentcollecting sex workers DNA in hopes of identifying their bodies should they wind up dead.
As a recent study from Duke University points out, for vulnerable populations, such data can be a double-edged sword. The same data that could help them also risks violating their genetic privacy, or worse, incriminating them should it be abused. Police have created, in essence, a DNA database of sex workers. Its not hard to imagine ways that could go wrong.
DNA databases have the potential to improve investigations into crimes impacting sex workers, who are more likely to be victims of murder than other populations, and often, do not carry any legitimate form of ID. Just as a decade ago some parents turned to fingerprinting to help identify their children in case they were kidnapped, the Dallas police started collecting DNA samples from sex workers just in case, god forbid, they wound up dead on the side of the highway. But while this kind of data might help police bring about justice for some of the grisliest crimes, it could also impinge upon sex workers privacy, coercing them into handing over information that could be indicting.
The social ramifications of collecting DNA from vulnerable populations (e.g., children, vagrant youth, sex workers, and victims of criminal acts) are considerable, and questions remain unanswered as to how best to protect individuals from misuse of their voluntarily provided DNA, write authors of the new study published in the International Journal of Criminal Justice Sciences.
Working with law enforcement, the authors went to Dallas to interview sex workers about the ongoing DNA collection program. Although many of the women said they do not trust police, they also said they willingly gave DNA samples because they want to be identified in the case of their death. The database has already helped to identify at least one woman, a sex worker who died in a Fort Worth ER in 2013.
My guy, the few times that I did talk to him while I was on the street, he always used to joke about the fact that they were going to tattoo my social security number and my address on my foot so that if I died that somebody knew who I belonged to, one focus group member said. That was one of the reasons why I did it. And then Ive had twofriends that have actually been identified through the program.
Still, some women were concerned about where their DNA might wind up.
One of my concerns would be who would have access to this information, once they got the DNA sample or whatever, who else would have access to it? another focus group participant said. Like would it be just for this simple organization or would everyonepolice, doctors, you know like people who go and donate sperm, sperm banks, stuff like thatlike who would have access to DNA?
As a society, we are just beginning to understand how important the right to genetic privacy is. Information about our DNA, if not properly handled and protected by law, could wind up not only incriminating people in criminal scenarios, but affecting access to things like insurance and employment. Right now, legislation is winding its way through Congress that seeks to undo some of the protections of the Genetic Information and Nondiscrimination Act. Many groups have spoken out against it, viewing it as a massive violation of public privacy.
The authors note that the police program has taken care to enact privacy protections, including only processing samples in the event of a death linked to a participant, and storing them in a facility not associated with law enforcement. But one participant suggested that a universal database, rather than one just for sex workers, and a program run outside of law enforcement entirely might make the program more egalitarian.
The Dallas program is a good example of the increasingly complicated position that DNA occupies in modern life. On the one hand, it can provide miraculous information that helps solve crimes, identify disease and help tell us about who we are. On the other hand, that same information can be damning.
And while the DNA sampling program is billed as voluntary, the authors question how voluntary it can really be when the request is coming from the police. At the time of DNA collection, the participants are either already under courtsupervision from an arrest or in a treatment program, which places them in a position under law enforcement authority, and perhaps less able to provide true consent, the authors write.
The authors point out that the only way to walk that fine line between benefit and disaster is to do so with careful consideration of all the ways things might go wrong. In this case, that means taking into account the opinions of the population the police are DNA testing, to make sure they arent coercing vulnerable people into unwillingly giving up a right to privacy.
[The Atlantic]
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NY mulls use of DNA familial matching – Police News
Posted: at 10:48 am
Print The draft policy says that before familial searching is done, local police have to certify that reasonable investigative efforts have been exhausted
By Anthony M. Destefano Newsday
NEW YORK A state panel of DNA experts approved on Monday a draft policy allowing familial searching, a new and controversial form of genetic testing, as a way of helping police solve homicide, certain sex crimes and terrorism cases.
By a unanimous vote, the DNA subcommittee of the state Commission on Forensic Science approved a short policy statement calling for familial searching, also known as FS, as well as a set of regulations to govern the procedure in New York.
The subcommittee also recommended that the commission approve the policy, which garnered interest as a result of the killing of Howard Beach jogger Karina Vetrano last August. Police got DNA from Vetranos body but couldnt get any matches with genetic profiles in the state DNA database.
The draft policy approved by the subcommittee said that before familial searching is done, the local police and prosecutors have to certify that reasonable investigative efforts had been exhausted or that emergency circumstances exist. It would also be used in investigations dealing with first-degree kidnapping and arson.
Interest increased in familial searching following a November 2016 story in Newsday which described familial searching and its potential use in the Vetrano investigation, which at that time seemed stalled. NYPD Commissioner James ONeill and Queens District Attorney Richard Brown issued strong statements calling for changes in state procedures to allow familial testing.
Todays action by the DNA Subcommittee of the NYS Commission on Forensic Science unanimously approving familial match DNA searches is an important step forward in identifying the guilty, excluding the innocent and bringing closure to the families of victims of unsolved homicides, Brown said in a statement. While the journey for justice for those families is not yet complete, this is an important milestone.
The Vetrano family also support the testing, even though police, using more traditional investigative methods, were finally able to make an arrest in early February of a suspect in Karinas homicide.
Some civil libertarians have voiced concerns about privacy and the fact that the existing state DNA database has a disproportionately high number of profiles of people of color. Proponents said familial searching is race-neutral.
2017 Newsday
McClatchy-Tribune News Service
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Watching the passage of knotted DNA slip through nanopores … – Science Daily
Posted: at 10:48 am
Science Daily | Watching the passage of knotted DNA slip through nanopores ... Science Daily How can long DNA filaments, which have convoluted and highly knotted structure, manage to pass through the tiny pores of biological systems? Scientists used ... |
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Shale Gets Another Efficiency Boost – DNA Testing Can Cut Costs By 10% – Seeking Alpha
Posted: at 10:48 am
source: Stock Photo
If competitors didn't have enough to worry about concerning U.S. shale, another technological breakthrough has the potential to slash another 10 percent off of production costs for shale companies, further enhancing their ability to boost supply and generate a profit under most oil price points.
Among the more than dozen companies using Biota Technology's DNA testing are Statoil ASA (NYSE:STO) and EP Energy Corp. (NYSE:EPE).
To get an idea of the potential range of costs, shale wells are developed from $4 million to $8 million, depending on a variety of elements involved. Biota's take from those using the technology is under 1 percent, said Ajay Kshatriya, CEO and co-founder of Biota Technology.
Peter Lascelles, a geologist for EP Energy Corp., which was one of Biota's first customers, said DNA testing is superior to seismic and chemical analysis in understanding well performance and their potential.
What DNA testing is and does
The outcome of using DNA testing is it allows drillers to avoid mistakes which could limit the maximum output potential of a given well. It helps to more accurately measure the amount of pressure needed to reach shale oil, as well as allows drillers to know beforehand the distance needed between wells to generate the best results, among other improvements.
"The technique involves testing DNA extracts from microbes found in rock samples and comparing them to DNA extracted from oil. Similarities or differences can pinpoint areas with the biggest potential," according to Reuters.
Not only does this help companies engage in less costly production methods because of less accurate knowledge, but it also helps improve productivity by cutting the time it takes for a company to start pumping oil.
Being skeptical of yet another assertion of technology that can improve costs, EP Energy made Biota participate in a blind test to see how effective the technique was. It asked the company to make a determination on the origination of a specific oil sample from numerous wells in a targeted zone.
Lascelles said the company in fact did pinpoint the wells the oil sample came from and was as a result able to recommend ways it could improve drilling in the area.
At under 1 percent of costs to bring wells into production, it's easy to see why this is a very desirable technology to include in the output process.
source: Reuters via Biota
Concerns over increased supply misguided
Earlier in March, Bloomberg published an article where concern was aired over the lower costs of shale oil bringing more supply to the market, which would drive down the price of oil. In my view this is misguided and the result of not understanding how business works.
It would be no different than Wal-Mart at the height of its power being considered a weak investment because its low prices and margins generated more sales, which in turn may provide it the room to further lower prices. The same could be said about Amazon and it removing a lot of the costs out of distribution and delivery, which increases the sales at the company.
Rising supply is a major problem only if the costs are rising while the price of oil is falling. Otherwise, companies can profitably boost revenue and earnings at a lower price point than in the past.
Just like with retailers that turn over inventory far more than competitors and make money by increased sales, oil producers generate more revenue and earnings by increasing barrels sold, even if the price of oil has dropped. They make less per barrel but more from increased sales. Volume makes up for it.
I'm referring here to the new wells being completed, as the older wells aren't as efficient as the new wells. Once the old wells are worked through, the shale industry will emerge as among the lowest cost producers outside of a few state-owned companies in the Middle East. But even with that in mind, the shale costs are being driven down so much they could come close to those costs within the next year or two.
If you think that's too optimistic of an outlook, at CERAWeek some executives said breakeven was a low as $12 per barrel. Shell (NYSE:RDS.A) has said its new wells start to be profitable at about $20 per barrel. It's not going to be long before even those low numbers are improved.
EP Energy
At the end of 2016 EP Energy had drilling inventory of about 5,200 locations, with 2,900 of them located in the Wolfcamp.
The company noted in its latest earnings report that almost all of its locations are profitable "at today's strip pricing," and over 80 percent of them are profitable under $40 per barrel.
Cash costs in 4Q 2016 dropped 7 percent year-over-year, with most of the expense categories lower. Adjusted EBITDA was $255 million in the fourth quarter.
Also important on the cost side, the company was able to get its lease agreements amended with its landowner, the University Land System, which cut back on the royalty rates it will have to pay.
It's easy to see with increased productivity, lower costs and lower royalties, how the company has positioned itself for stronger earnings. Add to that the improvements it'll get from incorporating DNA testing into its operations, and you can see things are going to get better going forward.
And even if the price of oil finds support and royalties climb once again, it doesn't take away from the benefit it gets on the cost side from DNA testing.
Add to that its hedging of 75 percent of its 2017 oil product at $61.66 and its 76 percent of its natural gas production at $3.28, the company looks like it could outperform through the remainder of 2017.
Further out, the company has hedged about 20 percent of its 2017 production level at $60 per barrel, and over 25 percent of its natural gas swap at $3.11.
Statoil
Statoil doesn't have the same performance outlook at EP or others working shale have, as its locations aren't as profitable as the Permian is. Its major deposits are in the Bakken, Eagle Ford, and Marcellus.
So far Statoil hasn't been able to match many of its competitors on the efficiency side, as its breakeven point at the end of 2016 was a very high $66 per barrel. Even so, that's still an 35 percent improvement over 2015 costs. The company says by 2018 it should be able to cut breakeven down to $50 per barrel.
That is based upon existing inventory. If it were to acquire acreage in the Permian, it would be able to more rapidly lower its outlook for breakeven.
Embracing technology that can improve its cost structure will help Statoil, especially has it plays catch-up with competitors that have rapidly improved their ability to compete at most oil price levels.
Conclusion
Continuing to remove costs out of the production process is a positive for the shale industry, as it can continue to increase production profitably with their new wells.
Not only is this not bad, it's very good, as it puts more pressure on OPEC and Russia, which don't have a lot of room to lower costs. In regard to OPEC, I'm talking about the low-cost leaders, which also happen to be the top suppliers within the cartel. Russia actually has significant shale reserves, but its exposure to high-cost Artic oil and the ongoing restrictions on acquiring Western tech and equipment, which would boost its performance, makes it difficult for Russia to make cost improvements at this time.
Those with exposure to U.S. shale know that it's the future of oil for at least the next couple of decades. Costs are going to continue to improve, and when they're very close to the best OPEC has to offer, they'll crush the cartel. Already the U.S. is the swing producer. What happens when costs are removed to the point of being almost even with the best OPEC has to offer?
We're not going to see shale producers cutting back on production. It'll be measured and disciplined, but not relevant to concerns on rising supply and lower oil prices offsetting lower costs. It's U.S. shale that has the rest of the world on the ropes, not the other way around.
That doesn't mean high-cost shale producers won't come under pressure, because they will. What it means is the very best companies are starting to rise to the surface, and as they take more market share from competitors, the industry will consolidate further, and they will be in almost complete charge of the direction of oil in the not too distant future.
In my view this is OPEC's last time of attempting to manipulate the price of oil by cutting costs. Shale producers have responded to the cuts by ramping up production. The problem is many investors and analysts continue to interpret this as the result of moderately higher oil prices, when the reality is it's because they can generate profits with oil at a much lower level. That's why an increase in supply is to the benefit of shale producers; they don't have to provide for a country like its OPEC competitors do.
As for DNA testing, it's one more arrow in the quiver of shale producers who have another tool to use to cut costs even further.
Disclosure: I/we have no positions in any stocks mentioned, and no plans to initiate any positions within the next 72 hours.
I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.
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For black Mormons, DNA testing a revelation of roots and faith – Salt Lake Tribune
Posted: at 10:48 am
Then, for Giddins' birthday, a friend gave him an AncestryDNA test kit. He put the $99 gift on the shelf and forgot about it.
"One day, in spring 2016, I took it down and looked at it. I thought to myself, 'I should take this thing. I've been looking for my mom all this time,'" Giddins recalls. "So, I did it. I took the test."
Using the kit's prepaid packaging, Giddins mailed a sample of his saliva to AncestryDNA for analysis of maternal and paternal genetic information ("autosomal DNA," or all 23 pairs of chromosomes). A few weeks later it can take six to eight weeks he was notified that his results were available online.
"They give you links to everyone [in the testing database] you share DNA with," Giddins says. "I found my mom and much more. I found a brother, two sisters, cousins, aunts and uncles. I found my history; I found my truth."
Giddins' biological mother, now 70 and living in Columbia, S.C., called him, knowing only that her family tree indicated that they somehow were related. As they talked, she asked for his birthday.
"Dec. 17," he answered.
"She said, 'I am the woman on your birth certificate.' We both cried," Giddins says. "She told me that on every Dec. 17, she had prayed to God that I was well."
Giddins, his wife, Lita, and their five children have since visited his rediscovered relatives in South Carolina, and he talks with his biological mother two or three times a week on the telephone.
"We have a lot to catch up on," he laughs.
Spokeswoman Crista Cowan said that while Lehi-based AncestryDNA provides clients with ethnicity breakdowns, it does not keep specific records of customers' race or religion. That said, there seems ample anecdotal evidence (a search of YouTube using the term "African-American DNA testing" turns up more than 40,000 results) of black people using AncestryDNA and other testing companies to plumb their roots.
"A lot of people are creating videos of their DNA 'reveals,'" Cowan says, adding that many customers are surprised at the ethnic diversity discovered within their chromosomes.
Overall, AncestryDNA has seen orders for its kits skyrocket since the service launched in May 2012. More than 3 million people have tested, with that number having jumped from just 2 million in spring 2016.
As life-changing as DNA testing has proved for African-American clients in general, it allows blacks who have embraced Mormonism to do what other Latter-day Saints take for granted identify ancestor candidates for baptismal temple rites for the dead.
Robert Burch Jr., president of the Utah chapter of the Afro-American Historical and Genealogical Society, found DNA results in 2016 that took him beyond his slave forebears, all the way to ancestors in the Cameroon and Congo regions several centuries ago.
"I encourage African-Americans to do DNA testing," Burch says. "It allows us to leap across the obstruction of 600 years of racial lies and historic deletions."
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For black Mormons, DNA testing a revelation of roots and faith - Salt Lake Tribune
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New study investigates the passage of knotted DNA through nanopores – Phys.Org
Posted: at 10:48 am
March 29, 2017 How can long DNA filaments, which have convoluted and highly knotted structure, manage to pass through the tiny pores of various biological systems? This is the fascinating question addressed by Antonio Suma and Cristian Micheletti, researchers at the International School for Advanced Studies (SISSA) in Trieste who used computer simulations to investigate the options available to the genetic material in such situations. The study has just been published in PNAS, the journal of the National Academy of Sciences of the Unites States. Credit: Antonio Suma, SISSA
Anyone who has been on a sail boat knows that tying a knot is the best way to secure a rope to a hook and prevent slippage. Similarly, knots in sewing threads prevent them slipping through two pieces of fabric. How, then, can long DNA filaments, which have convoluted and highly knotted structure, manage to pass through the tiny pores of various biological systems? This is the fascinating question addressed by Antonio Suma and Cristian Micheletti, researchers at the International School for Advanced Studies (SISSA) in Trieste, who used computer simulations to investigate the dynamics of the molecule in such situations. The study has just been published in PNAS, the journal of the National Academy of Sciences of the Unites States.
"Our computational study sheds light on the latest experimental breakthroughs on knotted DNA manipulation, and adds interesting and unexpected elements," explains Micheletti. "We first observed how knotted DNA filaments pass through minuscule pores with a diameter of about 10 nanometers (10 billionths of a meter). The behaviour observed in our simulations was in good agreement with the experimental measurements obtained by an international research team led by Cees Dekker, which were published only a few months ago in Nature Biotechnology. These advanced and sophisticated experiments marked a turning point for understanding DNA knotting. However, current experiments cannot detect how DNA knots actually pass through the narrow pore.
"In fact, the phenomenon occurs over a tiny spatial scale that is inaccessible to microscopes. This is why our group resorted to what the great German biophysicist Klaus Schulten called 'the computational microscope,' that is, computer simulations."
Suma and Micheletti explain: "The simulations revealed that the passage of the knot can occur in two distinct ways: One where the knot is tight, and the other where the knot is more delocalised. In both cases, the knot not only passes through the pore, but it does so in a very brief time."
Moreover, the knot usually passes in the final stages of the translocation, when most of the DNA strand has already passed. "But there is something more that is counterintuitive," state the authors. "The size of the knot, whether small or large, does not seem to affect the pore obstruction time by much. The latter depends instead on the translocation speed, which, in turn, depends on the initial position of the knot along the filament." These results, say the researchers, ought to help the design of future experiments probing the spontaneous knotting of DNA, a still largely unexplored venue, especially regarding the size of DNA knots.
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Advancing our current understanding of knots in biological molecules is important to clarify their implications in biological contexts as well as in applicative ones, such as DNA sequencing using nanopores. Suma and Micheletti hope that the promising directions suggested by their study can lead to a more detailed and accurate profiling of entanglement in DNA, RNA and proteins.
Explore further: New study shows that proteins are 'virtually' knotted
More information: Antonio Suma et al. Pore translocation of knotted DNA rings, Proceedings of the National Academy of Sciences (2017). DOI: 10.1073/pnas.1701321114
Journal reference: Proceedings of the National Academy of Sciences Nature Biotechnology
Provided by: Scuola Internazionale Superiore di Studi Avanzati
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New study investigates the passage of knotted DNA through nanopores - Phys.Org
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