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Category Archives: Transhuman News

Scientists thought ancient Egyptian mummies didn’t have any DNA left. They were wrong – Science Magazine

Posted: May 30, 2017 at 2:03 pm

Scientists successfully sequenced DNA from mummies from the site of Abusir el-Meleq, one of which was buried in this sarcophagus.

bpk/Aegyptisches Museum und Papyrussammlung, SMB/Sandra Steiss

By Lizzie WadeMay. 30, 2017 , 11:00 AM

Ancient Egyptian mummies preserve many details of the deceased: facial features, signs of illness, even tattoos. But not, it seemed, DNA. After trying repeatedly to extract it, may scientists were convinced that the hot desert climate and, perhaps, the chemicals used in mummification destroyed any genetic material long ago. Now, a team of ancient DNA specialists has successfully sequenced genomes from 90 ancient Egyptian mummies. The game-changing results give scientists their first insight into the genetics of ordinary ancient Egyptianswhich changed surprisingly little through centuries of conquests.

The sequencing success, reported this week in Nature Communications, finally proves to everyone that theres DNA preserved in ancient Egyptian mummies, says Albert Zink, a biological anthropologist at the Institute for Mummy Studies in Bolzano, Italy. He participated in a 2010 study that identified DNA sequences from 16 ancient Egyptian royal mummies, including Tutankhamun. But that study used polymerase chain reaction, a method that efficiently finds and extracts targeted DNA fragments but cannot always reliably distinguish between ancient DNA and modern contamination.

The new study, led by Johannes Krause, a geneticist at the Max Planck Institute for the Science of Human History in Jena, Germany, used next-generation sequencing methods to read stretches of any DNA present in a sample and fish outthose that resembled human DNA. The complete reads allowed the team to spot tell-tale damage patterns associated only with ancient DNA. That makes the new analysis much more reliable, says Hannes Schroeder, an ancient DNA researcher at the University of Copenhagen. It succeeds where previous studies on Egyptian mummies have failed or fallen short.

Krause, who has studied the DNA of Neandertals, Denisovans, and prehistoric migrants to Europe, recently gravitated toward ancient Egyptian mummies because of the empires tumultuous political history. At various points, it was conquered by Assyrians from the Near East, Nubians from farther south along the Nile, Persians, Greeks, and Romans, among others. Our question was, did those foreign conquests have a genetic impact? Krause says.

Krause turned to a collection of 151 mummy heads from the ancient settlement of Abusir el-Meleq, about 100 kilometers south of Cairo along the Nile. The settlement was devoted to Osiris, the god of the dead, making it a popular burial spot for many centuries. The heads were excavated (and removed from their bodies) in the early 20th century and now reside in two collections in Germany, at the University of Tbingen and Berlins Museum of Prehistory and Early History. Radiocarbon dating shows that the mummies span 1300 years of ancient Egyptian history, during many of the foreign conquests and then Egypts incorporation into first the Greek and then the Roman empires.

Whereasthe mummies soft tissue contained almost no DNA, the bones and teeth were chock full of genetic material. Ninety of the mummies yielded DNA once housed in mitochondria, the power plants of cells. Mitochondria carry only a few genes, but they are so plentiful that its often easier to find their DNA than the single full human genome in a cells nucleus. Still, because mitochondrial DNA is passed down from mother to child, it leaves out the story of the fathers DNA. The nuclear genome, which contains DNA from both parents, is far more informative. Unfortunately, Krause says, only a few of the mummies nuclear genomes were well preserved, and even fewer passed his strict contamination tests. His team ended up with nuclear genome samples from only three mummies, each from a different time period.

Krauses team compared the mummies mitochondrial and nuclear DNA to ancient and modern populations in the Near East and Africa. They discovered that ancient Egyptians closely resembled ancient and modern Near Eastern populations, especially those in the Levant. Whats more, the genetics of the mummies remained remarkably consistent even as different powers conquered the empire. Its possible that the mitochondrial genomes simply dont record the genetic contributions of foreign fathers, says Yehia Gad, a molecular geneticist at the National Research Centre in Cairo and a founder of the Egyptian Museums ancient DNA lab who worked with Zink on past mummy studies. But the three mummies with nuclear genome data also show striking genetic continuity, Krause points out.

Later, however, something did alter the genomes of Egyptians. Although the mummies contain almost no DNA from sub-Saharan Africa, some 15% to 20%of modern Egyptians mitochondrial DNA reflects sub-Saharan ancestry. Its really unexpected that we see this very late shift, Krause says. He suspects increased trade along the Nileincluding the slave tradeor the spread of Islam in the Middle Ages may have intensified contact between Northern and sub-Saharan Africa.

Geneticist Iosif Lazaridis of Harvard Medical School in Boston, who studies how and when ancient populations mixed, calls the new results a big accomplishment. But he wonders how representative Abusir el-Meleq is of ancient Egypt as a whole. Egypt is a big place, he says. Other regions may have experienced its conquests in different ways, some perhaps with more genetic mixing. But Lazaridis hopes for more revelations to come. Now thatits been proven that its possible to sample from mummieswell, there are literally thousands of mummies.

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Va. crime commission to study expansion of DNA databank to include more people convicted of misdemeanors – Roanoke Times

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RICHMOND The Virginia State Crime Commission will consider expanding the state DNA database of convicted people by including more misdemeanors.

While a larger database of DNA profiles from offenders would help solve more crimes, further expansion of qualifying crimes raises cost and privacy concerns and is opposed by the ACLU of Virginia and others.

The commission staff will also review the adequacy of current safeguards against the unauthorized collection, retention or dissemination of DNA information collected by authorities and the money required for any additional collecting.

A bill that would have directed the crime commission to study expanding DNA collection did not pass in the General Assembly this year, but the commissions executive committee decided it wanted to do it anyway.

State Del. Rob Bell, R-Albemarle, the chairman of the commission, said, Im looking forward to the information our staff assembles as they review what has happened in Virginia and other states.

Among those in favor of the study are John and Susan Graham, parents of University of Virginia student Hannah Graham, who believe she would not have been murdered had her killers DNA been taken following a misdemeanor trespassing conviction in 2010.

Hannah Graham was abducted in Charlottesville and slain by Jesse Matthew Jr. in 2014. His DNA from the trespassing conviction would have generated a hit in 2010 linking Matthew to a 2005 sexual assault in Fairfax, and he would have presumably been in prison in 2014 instead of killing Graham.

As part ofa 2016 plea deal, Matthewpleaded guilty to killing Graham and 20-year-old Virginia Tech student Morgan Harrington of Roanoke County, who was abducted in October 2009 in Charlottesville.

The Grahams and expansion proponents like Albemarle County Sheriff J.E. Chip Harding and Commonwealths Attorney Robert Tracci say they hope the commission will look at which class one misdemeanor convictions in Virginia those punishable by up to a year in jail and a fine of $2,500 make the most sense for requiring samples.

According to the National Council of State Legislatures, two states, New York and Wisconsin, currently collect DNA samples from people convicted of all felonies and misdemeanors; two states collect for only some felonies and some misdemeanors; while 42 states, including Virginia, collect for all felonies and some misdemeanors.

The Virginia Department of Forensic Sciences website shows Virginias database, also called a databank, now holds more than 415,000 offender DNA profiles. DNA profiles recovered from crime scenes are compared looking for matches, or hits. The DNA profiles can also be compared to find matches between crimes and exonerate the innocent.

Virginia was the first state with its own database and had its first hit in 1993 when the assailant was identified in the vicious beating, rape and robbery of a 63-year-old Dale City woman. Virginias database profiles have now solved, or assisted in solving, more 10,000 crimes including 750 murders and more than 1,500 sexual assaults.

In Virginia most recently, nine misdemeanors were added in 2015. DNA is now currently collected from adults convicted of 14 primarily sex-related misdemeanors, but also for such misdemeanors as resisting arrest, stalking and the unauthorized use of a motor vehicle.

(DNA samples are also required in Virginia from: adults convicted of felonies and adults arrested for any violent felony and certain burglary crimes; juveniles, 14 or older at the time of the offense and convicted or adjudicated delinquent of any crime that would be a felony if committed by an adult; people registered with the Virginia Sex Offender and Crimes Against Minors Registry; and anyone ordered to provide a sample by a circuit court as part of a plea agreement. Profiles collected at the time of arrest are removed from the database if there is no conviction.)

Traci said he and Harding provided a host of topics they hope the commission staff will look at, among them the experience of New York and Wisconsin since those states expanded collection to include all misdemeanors and identify the serious misdemeanors that returned the most hits to unsolved crimes as a result of their expansions.

He also said they would like to see a review of current privacy protections to enhance transparency and confidence in the integrity of safekeeping and prevention of unauthorized dissemination of the collected DNA. That would also include possible stiffer penalties for the unlawful retention or dissemination of information.

Kristen Howard, executive director of the commission, indicated those areas will be examined. The commission will hear a report on the proposal at its Nov. 14 meeting.

Bill Farrar, a spokesman for the ACLU of Virginia, said, We would object to any expansion to the list of offenses for which DNA collection would be made mandatory.

Already, in our estimation, the list has grown beyond whats really appropriate. We dont think that this most personal and private of information should be collected from people who have only committed a misdemeanor, for example, Farrar said.

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Virginia studies DNA database expansion – WSET

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by Elizabeth Tyree, The Associated Press

RICHMOND, Va. (AP) -- Virginia officials are studying a DNA database expansion to include more people convicted of misdemeanors.

The Richmond Times-Dispatch reports that supporters expect a larger database to help solve more crimes, but opponents say an expansion raises cost and privacy concerns. The Department of Forensic Science's website shows Virginia's database now holds more than 415,000 offender DNA profiles.

A bill that would have directed the Virginia State Crime Commission to study an expansion didn't pass in the General Assembly this year, but the commission's executive committee decided to do it anyway. Staff will also review safeguards and the cost of any additional collections.

Among those in favor of the study are John and Susan Graham, parents of University of Virginia student Hannah Graham, who believe she would not have been murdered had her killers DNA been taken following a misdemeanor trespassing conviction in 2010, the Richmond Times-Dispatch reported.

Hannah Graham was abducted in Charlottesville and killed by Jesse Matthew in 2014.

Another supporter of the DNA database expansion is Gil Harrington, mother of Morgan Harrington who was also killed by Matthew.

Officials believe that Matthew's DNA would have generated a "hit" in the data bank after a sexual assault in Fairfax back in 2005 and, if convicted, Matthew would most likely have been in a jail cell instead of abducting Hannah Graham.

ACLU of Virginia spokesman Bill Farrar says and his group opposes collections from people who have only committed a misdemeanor.

The Associated Press contributed to this report.

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DNA tests tell LeMoyne Center youth who they are – Timesonline.com

Posted: at 2:02 pm

WASHINGTON, Pa. (AP) Alexandra Berumen thought she was European and Mexican. Wrong.

Serena Pierce thought she was Italian and German. Wrong.

Deitrick Stogner thought he was African-American. Partly wrong.

They and two other after-school program participants at LeMoyne Community Center - Kaprice Johnson and Daisean Lacks - submitted to DNA testing to determine their true ethnic makeup. They tested through ancestry.com and africanancestry.com in January, and four youngsters were surprised by the DNA results. One remains puzzled.

"No one is one thing. We're all a hodgepodge of many things," Joyce Ellis, executive director of the center, told a group of about 30 youngsters Thursday. They gathered in a room inside the East Washington center to watch a video related to the quintet's quest to find out - as Ellis put it - "Who do you think you are?"

Videographer Allen Bankz posed that question in January, after the five test subjects submitted saliva samples as DNA evidence. One by one, from behind his camera, he asked them what they believed their genealogies to be and recorded their responses. The interesting part would come later, when the results arrived and the kids would read them - for the first time - for a second filming.

The comparison of perception and reality promised to be interesting.

The results, though, came back later than Ellis expected. She was hoping to have them in time for the center's annual Black History Month celebration at the end of February, but the only ones to arrive by then were for Kaprice and for Ellis, who likewise wanted to be tested. The other results came in only recently.

Thursday afternoon, Alexandra and Serena were the only kids who did not know their true ancestries. Bankz was poised to film them a second time. The girls certainly weren't prepared for the results.

Alexandra, whose father owns Las Palmas, a Hispanic grocery in Washington, found out she is 57 percent American Indian and 36 percent European.

"Surprised?" Ellis asked, smiling.

"Mostly," said Alexandra, who looked mostly astonished.

Serena knew one great-grandmother was from Italy and that she had relatives from Germany and Ireland, but was semi-stunned to see she was 52 percent Irish, 15 percent Scandinavian and only 8 percent Italian.

Deitrick considers himself to be an African-American teen with a heavy concentration of relatives in the Chicago area. He also has a grandmother who is partly American Indian. But he is more European (52 percent) than African (43 percent), with a mix of many nations.

"I had no idea I was that much of a mix," he said.

Daisean has an interesting ancestral link. He is a descendant of Henrietta Lacks, who has gained renown as an unwitting contributor to amazing medical advances. Before she died of cervical cancer in 1951, at age 31, doctors removed two cervical samples without telling her. Henrietta's HeLa cells have been multiplied and used in a number of biomedical research procedures, and were instrumental in Jonas Salk's development of the polio vaccine.

In January, Daisean said his father is African-American, his mother is white and his family is mostly from Pittsburgh. He eventually discovered he is 33 percent Ivory Coast of Ghana, 21 percent Nigerian and 13 percent European. He was the only test subject who was not on hand for the DNA program Thursday.

Kaprice received her report more than two months ago and still considers it to be vague. She was told she has a gene that traces back about 15,000 years, and has a European background - without a breakdown of that background. Kaprice said a number of family members have hailed from around Carnegie and Pittsburgh, and that her mother is Irish with red hair.

Ellis also was surprised at her results, She said she is 36 percent European, with elements of France, Germany, England, Italy and Ireland - nations she, coincidentally, has visited. Ellis said she also is 24 percent West African descent.

"I'm zero percent native American Indian, which I thought might be the highest (percentage)," Ellis added.

Yet she wasn't totally surprised. When it comes to ancestry, the LeMoyne Center director realizes anything is possible.

"Skin tone is no matter," she told her young audience Thursday. "It's what the DNA says."

___

Information from: Observer-Reporter, http://www.observer-reporter.com

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Britain’s Got Talent’s Simon Cowell almost ruins DNA’s semi-final mind-reading act – DigitalSpy.com

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DNA asked Simon Cowell to turn to a page in a dictionary they'd provided page 1,414 if you're interested to find the word, but he had a bit of an issue.

Simon wasn't wearing his glasses and couldn't find the page, so Amanda Holden had to help him out, which was quite entertaining as a separate performance.

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Still, the word "probably" was indeed on the page and it was safe to say the act went down a treat with the judges, with Ant making fun of Simon's issue with the dictionary.

"Without glasses Ant, these are the smallest numbers I've ever in my life," he explained, before turning to the DNA chaps, gobsmacked.

"How the bloody hell did you do THAT? No seriously, I have no idea what just happened there, but that was honestly incredible."

David cheekily added: "What was truly magical, was that you got Simon Cowell to read a book for the first time in his life. That was incredible. I mean he didn't find it easy."

DNA battled it out in the first semi-final of the week alongside St Patrick's Junior Choir Drumgreenagh, PC Dan, Niels Harder, Kyle Tomlinson, Empire Dance Crew, Tyrone & Mina and Miss Treat Vibe.

Britain's Got Talent airs the show's live semi-finals all week on ITV.

Want up-to-the-minute entertainment news and features? Just hit 'Like' on our Digital Spy Facebook page and 'Follow' on our @digitalspy Twitter account and you're all set.

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‘Ladders’ let scientists measure lots of DNA for $10 – Futurity: Research News

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New, license-free DNA ladders offer a much cheaper way to estimate the size of DNA fragments.

Researchers developed two plasmidsa circular form of DNAthat DNA scissors known as restriction enzymes can cut to create the DNA ladders. The ladders can be used to estimate the size of DNA fragments between about 50 and 5,000 base pairs in length.

DNA ladders, also known as DNA molecular weight markers, are among the most commonly used reagents in molecular biology research, says Song Tan, professor of biochemistry and molecular biology at Penn State. They are used in any application that requires gel electrophoresisa technique that separates fragments of DNA by their size.

We would like to offer these plasmids to the research community as a means to produce high quality DNA molecular weight markers at a low cost.

The research team created two plasmids, pPSU1 and pPSU2, that together produce DNA ladders in increments of either 100 or 1,000 base pairs, depending on which restriction enzyme is used. Researchers can easily produce in their own laboratories enough of the two ladders for 1,000 uses for under $10. In contrast, commercially available DNA ladders cost between $250 and $500 for the same amount.

Additionally, unlike many currently available DNA ladders, the 100-base-pair ladders work appropriately on both agarose and polyacrylamide gels, two types commonly used in molecular biology.

We are also excited about the possibility that the pPSU plasmids may be used around the world to further research and enhance science education in classroom laboratories, says former undergraduate student Ryan C. Henrici. This technology produces DNA ladders at less than a penny per use, a fraction of the cost of using commercially available DNA ladders.

The pPSU1 and pPSU2 plasmids used to produce the Penn State DNA ladders will be available without licensing restrictions to nonprofit academic users through the Addgene and DNASU plasmid repositories.

The US National Institutes of Health National Institute of General Medical and the Penn State Eberly College of Science supported the work.A paper describing the research appears in Scientific Reports.

Source: Sam Sholtis forPenn State

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The first genome data from ancient Egyptian mummies – Phys.Org

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May 30, 2017 Map of Egypt, showing the archaeological site of Abusir-el Meleq (orange X), and the location of the modern Egyptian samples used in the study (orange circles). Credit: Graphic: Annette Guenzel. Credit: Nature Communications, DOI: 10.1038/NCOMMS15694

An international team of scientists, led by researchers from the University of Tuebingen and the Max Planck Institute for the Science of Human History in Jena, successfully recovered and analyzed ancient DNA from Egyptian mummies dating from approximately 1400 BCE to 400 CE, including the first genome-wide nuclear data from three individuals, establishing ancient Egyptian mummies as a reliable source for genetic material to study the ancient past. The study, published today in Nature Communications, found that modern Egyptians share more ancestry with Sub-Saharan Africans than ancient Egyptians did, whereas ancient Egyptians were found to be most closely related to ancient people from the Near East.

Egypt is a promising location for the study of ancient populations. It has a rich and well-documented history, and its geographic location and many interactions with populations from surrounding areas, in Africa, Asia and Europe, make it a dynamic region. Recent advances in the study of ancient DNA present an intriguing opportunity to test existing understandings of Egyptian history using ancient genetic data.

However, genetic studies of ancient Egyptian mummies are rare due to methodological and contamination issues. Although some of the first extractions of ancient DNA were from mummified remains, scientists have raised doubts as to whether genetic data, especially nuclear genome data, from mummies would be reliable, even if it could be recovered. "The potential preservation of DNA has to be regarded with skepticism," confirms Johannes Krause, Director at the Max Planck Institute for the Science of Human History in Jena and senior author of the study. "The hot Egyptian climate, the high humidity levels in many tombs and some of the chemicals used in mummification techniques, contribute to DNA degradation and are thought to make the long-term survival of DNA in Egyptian mummies unlikely." The ability of the authors of this study to extract nuclear DNA from such mummies and to show its reliability using robust authentication methods is a breakthrough that opens the door to further direct study of mummified remains.

For this study, an international team of researchers from the University of Tuebingen, the Max Planck Institute for the Science of Human History in Jena, the University of Cambridge, the Polish Academy of Sciences, and the Berlin Society of Anthropology, Ethnology and Prehistory, looked at genetic differentiation and population continuity over a 1,300 year timespan, and compared these results to modern populations. The team sampled 151 mummified individuals from the archaeological site of Abusir el-Meleq, along the Nile River in Middle Egypt, from two anthropological collections hosted and curated at the University of Tuebingen and the Felix von Luschan Skull Collection at the Museum of Prehistory of the Staatliche Museen zu Berlin, Stiftung Preussicher Kulturbesitz.

In total, the authors recovered mitochondrial genomes from 90 individuals, and genome-wide datasets from three individuals. They were able to use the data gathered to test previous hypotheses drawn from archaeological and historical data, and from studies of modern DNA. "In particular, we were interested in looking at changes and continuities in the genetic makeup of the ancient inhabitants of Abusir el-Meleq," said Alexander Peltzer, one of the lead authors of the study from the University of Tuebingen. The team wanted to determine if the investigated ancient populations were affected at the genetic level by foreign conquest and domination during the time period under study, and compared these populations to modern Egyptian comparative populations. "We wanted to test if the conquest of Alexander the Great and other foreign powers has left a genetic imprint on the ancient Egyptian population," explains Verena Schuenemann, group leader at the University of Tuebingen and one of the lead authors of this study.

Close genetic relationship between ancient Egyptians and ancient populations in the Near East

The study found that ancient Egyptians were most closely related to ancient populations in the Levant, and were also closely related to Neolithic populations from the Anatolian Peninsula and Europe. "The genetics of the Abusir el-Meleq community did not undergo any major shifts during the 1,300 year timespan we studied, suggesting that the population remained genetically relatively unaffected by foreign conquest and rule," says Wolfgang Haak, group leader at the Max Planck Institute for the Science of Human History in Jena. The data shows that modern Egyptians share approximately 8% more ancestry on the nuclear level with Sub-Saharan African populations than with ancient Egyptians. "This suggests that an increase in Sub-Saharan African gene flow into Egypt occurred within the last 1,500 years," explains Stephan Schiffels, group leader at the Max Planck Institute for the Science of Human History in Jena. Possible causal factors may have been improved mobility down the Nile River, increased long-distance trade between Sub-Saharan Africa and Egypt, and the trans-Saharan slave trade that began approximately 1,300 years ago.

This study counters prior skepticism about the possibility of recovering reliable ancient DNA from Egyptian mummies. Despite the potential issues of degradation and contamination caused by climate and mummification methods, the authors were able to use high-throughput DNA sequencing and robust authentication methods to ensure the ancient origin and reliability of the data. The study thus shows that Egyptian mummies can be a reliable source of ancient DNA, and can greatly contribute to a more accurate and refined understanding of Egypt's population history.

Explore further: 17 mummies discovered in central Egypt

More information: Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods, Nature Communications (2017). nature.com/articles/doi:10.1038/ncomms15694

Egyptian archaeologists have discovered 17 mummies in desert catacombs in Minya province, an "unprecedented" find for the area south of Cairo, the antiquities ministry announced Saturday.

New research published in Global Heart (the journal of the World Heart Federation) shows that there are no significant differences in the incidence or severity of atherosclerotic disease (narrowing of the arteries with fatty ...

(AP) -- Archeologists have unearthed 57 ancient Egyptian tombs, most of which hold an ornately painted wooden sarcophagus with a mummy inside, Egypt's Supreme Council of Antiquities said Sunday.

(Phys.org) The study and popular perception of Egyptian antiquities focuses too much on the unwrapping of mummies and the use of technologies such as scanning, according to an academic from the University of East Anglia.

As silent witnesses to the past, ancient Egyptian mummies can add to our knowledge of their society well beyond what we can learn from the study of texts, art and funerary rituals.

Egyptian archaeologists have unearthed several mummies, colourful wooden sarcophagi and more than 1,000 funerary statues in a 3,500-year-old tomb near the city of Luxor, hailing an "important discovery".

An international team of scientists, led by researchers from the University of Tuebingen and the Max Planck Institute for the Science of Human History in Jena, successfully recovered and analyzed ancient DNA from Egyptian ...

About 1 to 2 million years ago, early humans in East Africa periodically faced very dry conditions, with little or no water in sight. But they likely had access to hundreds of springs that lingered despite long dry spells, ...

The origin of animals was one of the most important events in the history of Earth. Beautifully preserved fossil embryos suggest that our oldest ancestors might have existed a little more than half a billion years ago.

In human history, the transition from hunting and gathering to farming is a significant one. As such, hunter-gatherers and farmers are usually thought about as two entirely different sets of people. But researchers reporting ...

A new species of a fossil pliosaur (large predatory marine reptile from the 'age of dinosaur') has been found in Russia and profoundly change how we understand the evolution of the group, says an international team of scientists.

People using smartphones are more likely to make rational and unemotional decisions compared to PC users when presented with a moral dilemma on their device, according to a new study from City, University of London.

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NRGene Assembles its 300th Crop Genome – DirectionsMag.com

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Ness Ziona, Israel May 30, 2017NRGene, the worldwide leader in genomic mapping, assembly, and referencing, has assembled 300 genomes of major crop plants in less than two years, enabling the highly accurate genome comparisons required to breed better seeds.

Before NRGenes technology, individual genomes took years to produce and then many more years to improve genome accuracy. With NRGenesDeNovoMAGICTM, the highest level of genome completeness and accuracy is achieved with a single assembly.

Over the past two years, assemblies have been created in cooperation with many of the worlds leading universities, government research institutes and non-for-profit organizations, as well as global companies like Syngenta and Monsanto.

DeNovoMAGIC 3.0delivers reference genomes quickly, accurately, and cost effectively, without requiring external data. It accelerates downstream analysis and reduces unnecessary technical work. DeNovoMAGIC assembles Illumina reads into long, phased sequences, delivering accurate assembly results, even from complex genomes, no matter the size, ploidy, or zygosity, for high quality genome mapping and productive breeding.

For crops with an existing reference genome, theDeNovoMAGICassemblies enable researchers to elucidate the vast genomic diversity that exists within the crop species. Scientists are using this critical information to breed more productive new varieties with the highest nutritional values.

Many full genomes now exist in most of the key crops, and NRGenesPanMAGICTMcombines the initial assemblies into an accurate genome-to-genome mapping to capture the full diversity of the crop varieties, including all types of sequence differences within the studied population, e.g. SNPs, InDels of any size, inversions, translocations, gene PAVs, and gene CNVs.

Breeding is all about making the most of a given genomic diversity in a given crop. If your goal is to make genomics applicable for breeding you must describe crop diversity accurately and affordably, says NRGene CEO Gil Ronen. Based on the feedback we get from our customers, were doing that and more allowing them to make major breakthroughs in the quest to increase the worlds food supply with more productive, hardier seeds.

About NRGene

NRGeneis a genomic big data company developing cutting-edge software and algorithms to reveal the complexity and diversity of crop plants, animals, and aquatic organisms for supporting the most advanced and sophisticated breeding programs. NRGene tools have already been employed by some of the leading seed companies worldwide as well as the most influential research teams in academia.www.nrgene.com.

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CRISPR gene tool can cause unintended flaws in genome – The … – Economic Times

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New York, May 30 (IANS) The CRISPR-Cas9 gene-editing technology can introduce hundreds of unintended mutations into the genome, warns a new study.

"We feel it's critical that the scientific community consider the potential hazards of all off-target mutations caused by CRISPR, including single nucleotide mutations and mutations in non-coding regions of the genome," said co-author Stephen Tsang, Associate Professor at Columbia University Medical Centre in the US.

CRISPR-Cas9 editing technology -- by virtue of its speed and unprecedented precision -- has been a boon for scientists trying to understand the role of genes in disease.

The technique has also raised hope for more powerful gene therapies that can delete or repair flawed genes, not just add new genes.

The first clinical trial to deploy CRISPR is now underway in China, and a US trial is slated to start next year.

But even though CRISPR can precisely target specific stretches of DNA, it sometimes hits other parts of the genome.

Most studies that search for these off-target mutations use computer algorithms to identify areas most likely to be affected and then examine those areas for deletions and insertions.

"These predictive algorithms seem to do a good job when CRISPR is performed in cells or tissues in a dish, but whole genome sequencing has not been employed to look for all off-target effects in living animals," co-author Alexander Bassuk, Professor at the University of Iowa, said.

In the new study, published in the journal Nature Methods, the researchers sequenced the entire genome of mice that had undergone CRISPR gene editing in the team's previous study and looked for all mutations, including those that only altered a single nucleotide.

The researchers determined that CRISPR had successfully corrected a gene that causes blindness, but they also found that the genomes of two independent gene therapy recipients had sustained more than 1,500 single-nucleotide mutations and more than 100 larger deletions and insertions.

None of these DNA mutations were predicted by computer algorithms that are widely used by researchers to look for off-target effects.

"We're still upbeat about CRISPR," co-author of the study Vinit Mahajan, Associate Professor at Stanford University, said.

"We're physicians, and we know that every new therapy has some potential side effects - but we need to be aware of what they are," Mahajan added.

--IANS

gb/dg

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One BioMed and A*STAR’s Genome Institute of Singapore establish joint lab – Enterprise Innovation

Posted: at 2:02 pm

Local diagnostics company One BioMed Pte Ltd and A*STARs Genome Institute of Singapore (GIS) have established a joint laboratory to develop molecular diagnostic assays for the Asian clinical infectious disease testing market.

The joint laboratory will focus on the full development and integration of the initial assays for the One BioMed platform. Each panel will be multiplexed and syndromic, and is expected to address clinically important infectious diseases in Asia, including pediatric respiratory infections, drug resistant tuberculosis and mosquito-borne illnesses. The laboratory will be located in the Genome building at Biopolis and will leverage the genomic expertise of GIS to improve the delivery of clinical medicine.

One BioMed recently spun-out of A*STARs Institute of Microelectronics (IME) is developing a point-of-care diagnostic platform deploying two proprietary technologies: a chemistry-based nucleic acid extraction and a silicon biophotonics dual-ring sensor. Integrated into a consumable cartridge design and run on a portable instrument, these approaches are expected to enable simple, cost-effective, rapid and highly multiplexed molecular testing outside of a central laboratory setting.

Dr Alexander Lezhava, Group Leader, Translational Research will lead the lab for GIS, and Dr Park Mi Kyoung, founder and Chief Technology Officer of One BioMed, will lead the lab for the company. We allied with the GIS Translational Research group because they combine extensive molecular diagnostics assay development expertise with regulatory and commercialisation experience, said Dr Park.

Prof Ng Huck Hui, Executive Director of GIS said, Our collaboration with One BioMed helps us address one of the most difficult problems facing patients and healthcare providers across the region poor access to accurate testing for infectious diseases like influenza, dengue and tuberculosis.

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One BioMed and A*STAR's Genome Institute of Singapore establish joint lab - Enterprise Innovation

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