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Category Archives: Transhuman News

ESA chief on space colonization: ‘Mars is not nice’ – Blasting News

Posted: June 3, 2017 at 12:03 pm

Life on Mars may soon be excluded from the sci-fi category. Elon Musk aims to move a million people to Mars, and renowned astrophysicist Stephen Hawking has said before that mankind has only 100 years to settle on another planet. Its a sad thought a space colony but if you ask the #European Space Agency, humanity ought to stay on Earth.

To find a new home outside of Earth, despite technological advancements, we still have a long way to go, according to ESAs Director General Johann-Dietrich Wrner. Even if we got there, it would be a foreboding experience for everybody.

Speaking with The Times, Dr. Wrner mentioned the Hollywood blockbuster The Martian. Matt Damon, who plays a stranded astronaut in the movie, has resorted to farming on Mars and along with his efforts are the various trudges he had to endure here and there.

The director implied that the astronauts experience is a walk in the park when compared to the harsh realities of actually living on the red planet.

Always you have to be sheltered and covered, but you cannot even bring your dog to the next tree," Dr. Wrner said. "Mars is not nice.

In the same interview, Dr. Wrner put emphasis on the difference between colonizing a planet and visiting one. Colonization is the wrong word, he asserted. What works instead as the operative term for establishing a life outside of Earth is visitation.

The idea of exploring other planets and moons had always been there, but the move to bring life beyond Earth recently had come to light. Advocates began sprouting, Musk being one of them, founder of SpaceX. While Mars is the most common choice to establish a colony, the moon isnt far off.

However, life on the moon is no different from living on Mars, according to the ESA head.

Daytime on one side of the moon lasts about 13 and a half days, followed by 13 and a half nights of darkness. When sunlight hits the moon's surface, the temperature can reach 253 degrees F (123 C). The "dark side of the moon" can have temperatures dipping to minus 243 F (minus 153 C). With this fact, Dr. Wrner said it wouldn't be "a nice life."

As scientists continue their search for extraterrestrial life, what theyre usually looking for are planets that are within a certain range of their host star, called the habitable zone. In that orbit distance, the planets are just in the right radiation levels to support life as know it. In our case, the Earth is not so far from the sun that it freezes into a rock of ice, and its not so close either that bodies of water boil into a gas.

But with Earth on the brink of destruction, reports of exoplanets have presented the possibility of life beyond the living planet. Whats interesting is that Dr. Wrner believes its better for humankind to stay, and is hoping somehow, well find a way to preserve life right where we are. #life on Mars #Colony On Mars

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ESA chief on space colonization: 'Mars is not nice' - Blasting News

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Egyptian mummy DNA shows Mediterranean, Turkish and European …

Posted: at 12:02 pm

Ancient Egyptians were an archaeologist's dream. Theyleft behind intricate coffins, massive pyramids and gorgeous hieroglyphs, the pictorial writing code cracked in 1799. Egyptians recorded tales of royalty and gods. They jotted downlife's miscellanies, too, as humdrum as beer recipes anddoctor's notes.

But there was one persistent hole in ancient Egyptian identity: their chromosomes. Cool, dry permafrost can preserve prehistoric DNA like anatural freezer, but Egypt is a gene incinerator. The regionis hot. Within the mummies' tombs, where scientists would hope to findgenetic samples, humidity wrecked their DNA. What's more, soda ash and other chemicals used by Egyptian embalmers damaged geneticmaterial.

A study led by researchers at the Max Planck Institute for the Science of Human History and the University of Tubingen in Germany managed to plug some of those genetic gaps. Researchers wrunggenetic material from 151 Egyptian mummies, radiocarbon dated between Egypt'sNew Kingdom (the oldest at 1388 B.C.) to the Roman Period (the youngest at 426 A.D.), as reported Tuesday in the journalNature Communications.

Johannes Krause, a University of Tubingen paleogeneticist and an author of the study, said the major findingwas that for 1,300 years, we see complete geneticcontinuity. Despite repeated conquests of Egypt, by Alexander the Great, Greeks, Romans, Arabs and Assyrians the list goes onancient Egyptians showed little genetic change.The other big surprise, Krause said, was we didn't find much sub-Saharan African ancestry.

The remains came from Abusir el-Meleq, an ancient Nile community in the middle of Egypt. From the mummies the scientists extracted bone, teeth and soft tissue samples. (Although Egyptian embalmers removed thebrains of the deceased, the scientists wrote that in most cases, non-macerated mummy heads still have much of their soft tissue preserved.)

The hard samples yielded the most DNA, perhaps because the teeth and bones were protected by soft tissue or because the embalming processes left tougher material intact.After preparing the samples in a sterilized room in Germany, the researchers bathed the samples in UV radiation for an hour to minimize contamination.

Ancient Egyptianswere closely related to people who lived along the eastern Mediterranean, the analysis showed. They also shared genetic material with residents of the Turkish peninsula at the time and Europe.

Given Egypt's location at the intersection of Africa, Europe and Asia, and the influx of foreign rulers, Krause said he was surprised at how stable the genetics seemed to be over this period. The scientists were particularly interested in the change in ruling class at the turn of the first millennium. First came the Hellenistic dynasty, in the aftermath of Alexander the Greats conquests, from 332 B.C. to 30 B.C., and thenRoman rule from 30 B.C. to about 400 A.D. And yet the genetics of the Abusir el-Meleq community appeared to be unperturbed by shifting politics.

The scientists compared these ancient genetics with those of 100 modern Egyptians and 125 modern Ethiopians that had been previously analyzed. If you ask Egyptians, they'll say that they have become more European recently, Krause said. We see exactly the opposite, he said.

It was not until relatively recently inEgypt's long history that sub-Saharan geneticinfluences became more pronounced.In the last 1,500 years, Egypt became more African, if you want, Krause said.

In their paper, the researchers acknowledged that all our genetic data were obtained from a single site in Middle Egypt and may not be representative for all of ancient Egypt. In the south of Egypt, the authors wrote, sub-Saharan influences may have been stronger.

This study left two gaps in the Egyptian timeline that Krause wants to fill, he said. It is not clear when theAfrican gene flow, present in modern Egyptians, occurred. Nor could the study determine theorigin of the Egyptians.The other big question is, 'Where did the ancient Egyptians come from?' Krause said. To answer that, scientists will have to find genomes back further in time, in prehistory.

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Chesterfield teen ID’d as rape suspect through DNA "cold hit" pleads no contest in 2015 attack – Richmond.com

Posted: at 12:02 pm

A Chesterfield County teen who was identified through the states DNA databank as a suspect in the 2015 rape and beating of a 47-year-old Chesterfield woman was convicted Friday of maliciously wounding her in a random attack.

In a deal struck by the prosecution and defense after the teens first trial on rape and sodomy charges ended with a hung jury, Quaseer L. Carter, 18, pleaded no contest to the felony count in the Oct. 7, 2015, attack. The woman was raped, sodomized and struck twice in the face after she was dragged off the street into a grassy area between two homes, according to evidence at Carters first trial in late March.

The plea agreement was reached after both sides recognized they faced substantial credibility issues with their respective cases. The victim, who attended Fridays proceeding in Chesterfield Circuit Court, was on board with the decision, Chesterfield prosecutor Stephen Sharpe told the court.

On the day of the attack, the victim was helping her former husband pack up some items for an upcoming trip at his home in the 2900 block of Goolsby Court, Sharpe said in a summary of evidence. At one point, she left and walked down Goolsby Avenue to a friends house less than a quarter-mile away to socialize.

She drank some beer with her friend before eventually leaving to walk back to her former husbands home at about 9 p.m. She was only a few houses away when a black male stopped her and asked for a cigarette, Sharpe said in his summary.

As the victim looked for a cigarette, the suspect struck her in the face in a blow that knocked her to the ground. The man then sexually assaulted the woman before raising her to her knees, when he struck her again in the face. She again was knocked to the ground.

The victim testified at Carters first trial that something must have startled the suspect, because he jumped up quickly and ran off.

The victim managed to stumble back to her former husbands house, where police were immediately called. The woman suffered several scratches and cuts, a bloodied face and other injuries to her body, Sharpe said.

The suspect was wearing dark pants and a dark-hooded sweatshirt with the hood pulled down tightly over his face. It was dark outside, and the victim was unable to make out his facial features, according to evidence.

After the victim reported the attack to police, she was taken to a local hospital, where a physical evidence recovery kit was used to collect semen and other biological evidence.

The recovered evidence was sent to the Virginia Department of Forensic Science, where a sample was entered into the departments computerized DNA databank that contains the DNA profiles of hundreds of thousands of convicted felons. A match was made that identified Carter as a suspect.

Carters genetic fingerprint had been added to the database after his conviction as a juvenile in Richmond on a charge of felony theft from a person. Under Virginia law, juvenile offenders ages 14 or older and convicted of a felony are required to submit a DNA sample, the same as adult offenders.

Two weeks after the Oct. 7, 2015, attack on the woman, Carter was arrested in a carjacking that occurred just two days after the Goolsby Avenue assault. But a Chesterfield jury acquitted him of that charge at his April 21 trial.

At his rape trial, Carter claimed in testimony that his victim had propositioned him for sex in exchange for money an accusation that prosecutors said the woman would emphatically deny. The teen offered no explanation for the injuries she sustained during the attack. But he claimed she filed charges against him as an act of revenge, because she was angry that he only had $5 to pay her for sex.

Carter, who was 16 at the time and lived in the area, testified that he was walking home to dinner when he encountered the woman.

The teen faces up to five years in prison when he is sentenced in September. The judge allowed him to remain free on bond, but he remains under electronic monitoring with an ankle bracelet.

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Chesterfield teen ID'd as rape suspect through DNA "cold hit" pleads no contest in 2015 attack - Richmond.com

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Dutch families win right to test DNA of sperm bank doctor – BBC News

Posted: at 12:02 pm


BBC News
Dutch families win right to test DNA of sperm bank doctor
BBC News
A Dutch court has approved a request by families seeking DNA tests on the belongings of a late fertility clinic doctor accused of using his own sperm in dozens of cases. Jan Karbaat is suspected of fathering about 60 children at the centre he ran in ...
DNA tests allowed in IVF doctor scandal, Dutch court rulesDeutsche Welle
Dutch court allows posthumous DNA tests on doctor in IVF scandalThe Guardian
Court allows DNA tests on fertility doctor accused of sperm swapNew York Daily News
The Hindu -UPI.com -Sky News
all 11 news articles »

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Dutch families win right to test DNA of sperm bank doctor - BBC News

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DNA analyst: Muscle tissue delivered to downtown Greenville is ‘pretty unique case’ – WYFF Greenville

Posted: at 12:02 pm

GREENVILLE COUNTY, S.C.

A Greenville County DNA analyst says the case of a piece of muscle tissue being found in a container in downtown Greenville is a pretty unique case.

Greenville police said they were called to the CVS on Main Street Thursday about a shipping container that appeared to have a piece of muscle inside of it.

The coroner said a preliminary evaluation shows that the tissue is not a tongue, but appears to be skeletal muscle of some kind. DNA testing will be done to determine if it is human or animal.

Brian Browning, the DNA analyst for Greenville County Forensics, will do the testing on the tissue.

Its a mystery. Thats the reason theyre trying to investigate it. They dont know, number one, is it human? And number two, where did it come from and how did it get there, Browning said.

Browning said he will take samples of the tissue, extract the DNA and then determine how much human DNA, if any, is in the sample.

This is a pretty unique case, I gotta say. Getting tissue samples in general is pretty unique for us, but in this particular instance, getting that phone call was a new type of phone call, Browning said.

Police said the container appears to have originated in North Carolina and traveled through Georgia before arriving in Greenville.

They said detectives are working to track down the container's origins to see if an industrial or other accident may have occurred, or if there's any other explanation for the tissue.

Police said the container also held other products, but none of the products were meat- or dairy-related.

The tissue was being taken to the Greenville County Law Enforcement Center, and it will be evaluated by forensic investigators, Kent Dill, with the coroner's office, said.

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DNA analyst: Muscle tissue delivered to downtown Greenville is 'pretty unique case' - WYFF Greenville

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First-ever look at DNA opening reveals initial stage of reading the … – Phys.Org

Posted: at 12:02 pm

June 2, 2017 by Hayley Dunning Proteins interacting with the DNA strand. Credit: Imperial College London

Scientists have watched a cell's genetic machinery in the first stages of 'reading' genes, giving a potential way to stop the process in bacteria.

By reading certain genes - a process known as transcription - cells can produce and regulate proteins, which perform almost all the functions necessary for life.

In the new study, researchers used an extremely powerful technique called cryo-electron microscopy to physically see how this process happens in detail, for the first time. The insights could help researchers target this stage of transcription in bacteria with new antibiotics.

DNA is composed of two strands, which are normally linked together in a twisted helical structure. The strands are pulled apart by several specialist molecules that 'melt' it preventing the strands from coming back together as they normally try to do. This step in transcription usually happens very quickly, with a lot of changes occurring over a short time span, meaning it has been impossible to track in detail before.

In the study published today in Molecular Cell, the research team led by scientists at Imperial College London viewed the DNA opening in action.

Since transcription of DNA is so fundamental to the functioning of a cell, the team believe that knowing how it operates in bacteria could provide avenues for blocking the process, potentially shutting down the actions of harmful infections.

New ways to stop bacteria

Lead researcher Professor Xiaodong Zhang, from the Department of medicine at Imperial, said: "Bacteria are becoming increasingly resistant to antibiotics, so our insights into the first stage of transcription provide new ways of thinking about stopping bacteria.

"Understanding how the fundamental machinery works hopefully gives us additional tools for developing new kinds of antibiotics. As we investigate more steps in the process of transcription, we may find more stages during which we can intervene and attack harmful bacteria."

The process of transcription occurs in all living things and plays a crucial role in many cellular processes, including those related to diseases like cancer. The new insights might therefore apply across a whole range of organisms and disease processes.

Activating transcription

In particular, the team studied the action of a protein called sigma54, which controls a wide range of bacterial defences, holding them back until they need to be used. If drugs could be designed to interfere with this step, and preserve sigma54's power to hold back defences, they could make bacteria more vulnerable to attack.

Sigma54 unleashes the bacterial defences after being activated by a protein that changes sigma54's shape. The 'activator' protein, together with sigma54, then forms a protein wedge that drives the two DNA strands apart. The bacterial defence genes are then read and kicked into action.

The researchers were able to watch this transcription process in detail, giving them new insights into how they might use sigma54 to disable the bacteria's defences.

Study co-author Professor Martin Buck, from the Department of Life Sciences at Imperial, said: "DNA contains genetic information, which is converted to proteins that carry out all cell functions. Transcription is the first stage in accessing that information.

"It underpins all environmental adaptation in organisms it's how cells deal with their changing environments or even become abnormal, such as in cancer cells. Our work could therefore have implications across a range of biological processes."

Explore further: Discovery of trigger for bugs' defenses could lead to new antibiotics

More information: Robert Glyde et al. Structures of RNA Polymerase Closed and Intermediate Complexes Reveal Mechanisms of DNA Opening and Transcription Initiation, Molecular Cell (2017). DOI: 10.1016/j.molcel.2017.05.010

It is unusual enough to see one of nature's biggest, rarestnot to mention smelliestflowers bloom. But it is extraordinary to see two bloom at once.

As the United Nations Oceans Conference convenes in New York, a new paper calls on marine scientists to focus on social issues such as human rights violations in the seafood industry.

Scientists are now confident animal life on solid ground started with a few short bursts of marine creatures making the leap from the oceans.

Scientists have watched a cell's genetic machinery in the first stages of 'reading' genes, giving a potential way to stop the process in bacteria.

Passing skills down through the generations, previously thought to be unique to humanity, has been discovered in chimpanzees.

Once we start coloring our hair, we may be surprised to learn that we begin to have a problem in common with plant biologists: finding the right dye for our roots. In the case of the biologists, just the right chemical is ...

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Fact: The production and reproduction of life depends on the most complex, dense and miniaturized codes and coded information known to man.

Fact: the whole scientific community cannot understand the huge ammounts of DNA coded information.

Fact: codes and coded information are imaterial meanings ascribed to sequences of symbols (vg. A, T, G, C) and not matter or energy.

Fact: There is no natural law or physical process able to create meaningful codes and coded information.

Fact: There is no viable naturalistic explanation for the origin of life.

Fact: the molecular machines that transcribe, read and execute DNA coded information are thenselves coded in DNA.

Fact: random mutations are cumulative and degerative creating "noise", degrading information and causing disease, cancer, suffering and death.

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Fully sequenced deer genome made publicly available – Baylor College of Medicine News (press release)

Posted: at 12:01 pm

Researchers at Baylor College of Medicine have played a leading role in sequencing the whole genome of the common white-tailed deer, which has recently been made public by the National Center for Biotechnology Information.

The deer genome has the potential to provide insights into bone behavior, more specifically how deer are able to regenerate and repair bone after it is lost or damaged.

We are hoping that by understanding the deer genome in greater detail, we will be able to better consider how to approach and treat bone-related illnesses and disease, such as osteoporosis, said Dr. Brendan Lee, chair of the Department of Molecular and Human Genetics at Baylor. For example, antler growth each season is an example of the fastest and largest regenerating organ in nature.

By allowing the deer genome to be publiclyaccessible to researchers around the world, the NCBI is fostering collaboration among institutions when faced with solving complex cases or unidentified genetic conditions.

Sharing data is incredibly important in developing therapies for bone disease, added Lee, who also holds the Robert and Janice McNair Endowed Chair and Professor in Molecular and Human Genetics.

The sequencing of the deer genome was made possible through collaboration among the Center for Skeletal Medicine and Biology at Baylor, the Human Genome Sequencing Center at Baylor, the Rolanette and Berdon Lawrence Bone Disease Program of Texas, Berdon and Rolanette Lawrence, and the Caesar Kleberg Wild Life Research Institute. Prior to the publishing by the NCBI, the data was submitted to the National Institutes of Health.

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Team Maps Genome of Mojave Desert Tortoise – Arizona Public Media

Posted: at 12:01 pm

Researchers have finished the first full genome map of the threatened Mojave desert tortoise (Gopherus agassizii), also known as Agassizs desert tortoise.

Kenro Kusumi with Arizona State Universitys School of Life Sciences said the team hopes the data will aid conservation efforts, fill in blanks in the reptiles evolutionary history and perhaps offer clues to improving human health and longevity.

For diseases, were certainly interested in what makes them susceptible, the connection we study this in humans, too between their diet and their environment and their stresses, and their ability to fight off diseases," said Kusumi.

The research was published May 31 in PLOS ONE.

Mojave desert tortoises face threats from various quarters. Invasive grasses like red brome can stunt their early growth and may reduce their resistance to illnesses including upper respiratory tract disease (URTD), which afflicts the nose, nasal sinuses and trachea of some of the creatures. Humans threaten their survival by destroying habitat and building power lines, which provide new perches for predatory ravens.

Its a new habitat for the ravens. Its great for them, but its bad for baby tortoises, which they like to look at and then swoop down and eat, said Kusumi.

Based on comparisons with other existing reptile genomes, the study found changes in Mojave desert tortoise genes that regulate shell development, longevity and water conservation.

They also found that, among three desert tortoises (Mojave desert tortoise, Sonoran desert tortoise and Goodes Thornscrub tortoise), evolutionary forces seem to have differentiated protein sequences related to circadian rhythm the daily cycle of physiological and behavioral processes and the innate immune system.

The U.S. Fish and Wildlife Service listed the Mojave population that is located north and west of the Colorado River as threatened in 1990. Nevertheless, its numbers declined by about 50 percent from 2004 to 2013.

Understanding genetic variation and responses could help wildlife managers better grasp how disease and inbreeding affect the reptiles. Kusumi said it could also help scientist understand how the creatures adapt to their environs by isolating genes related to withstanding ultraviolet radiation and controlling urine volume.

We dont really know where the genetic treasure in the gold mine is. Where is the diversity that would allow the tortoise, as a species, to survive changes? said Kusumi.

A clearer picture of Mojave desert tortoises genetics and biodiversity could also improve management of reproduction and maintenance of habitat corridors, particularly under conditions of climate change. It would also help nail down the species geographical range, which overlaps with the Sonoran desert tortoise, aka Morafka's desert tortoise (Gopherus morafkai). The two desert tortoises sometimes mix boundaries and interbreed.

Were trying to answer, based on using the genome, where is the Mojave desert tortoise? Because we actually dont know exactly where that boundary is right now, said Kusumi.

Mojave desert tortoises live 40-50 years in the wild and more than 100 years in captivity. Dark green, with brown and yellow accents, they have rounded shells, stubby hind legs and flat front limbs built for digging. They occur in western Arizona, southern Nevada, Southern California and southwestern Utah. Kusumi said genetics could also offer clues as to how the species can live in such a diverse range of environments.

If you moved one from, say, Las Vegas to Southern California, it probably wouldnt do very well, because thats not the environment that its genome is making it suited for," he said. "So, within that species, wed love to know the genetic instructions that make a tortoise better suited for one place versus another.

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Repositive launches Personal Genome Project data collection – Business Weekly

Posted: at 12:01 pm

Repositive, the Cambridge company credited with creating the worlds largest portal for accessing human genomic research materials, has expanded the range of data available with the launch of a specialist collection for the Personal Genome Project.

The new PGP collection was formally unveiled this week at Repositives satellite symposium Finding and Accessing Human Genomic Data at EHSG in Copenhagen.

The initiative collates all the data collected for the Personal Genome Project in one place combining data currently held in the US, UK, and Austria.

The Personal Genome Project aims to sequence and analyse the genomes and medical records of 100,000 global volunteers. It contains large amounts of genomic data including whole genome sequencing, methylation analysis and RNA-Seq.

The new PGP specialist collection adds to Repositives series of community led data sets which include Autism, Microbiome, Personal Genomes, Population and Methylation collections.

CEO Fiona Nielsen (pictured) said: The Repositive Specialist Data Collections are already proving to be of significant benefit to many researchers. By collecting hard to find data in one place, we can ensure that researchers are able to quickly and easily find the data they need.

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Personal Genome Diagnostics Highlights its Patent-Pending Microsatellite Instability Testing Technology as FDA … – PR Newswire (press release)

Posted: at 12:01 pm

"This landmark FDA approval codifies the need to determine whether cancer patients potentially eligible for immuno-oncology therapy have microsatellite instability present in their tumors," said Doug Ward, CEO of PGDx. "It is particularly fitting that the approval involves MSI, a genomic condition whose relevance to cancer therapy was first uncovered by researchers at Johns Hopkins, with assistance from researchers at PGDx. We were thrilled to license rights to the patent-pending MSI measurement technology for immuno-oncology applications developed at Johns Hopkins, and are proud to be the first to offer it in both tissue and liquid biopsy formats. PGDx is also planning to submit a tissue-based MSI assay for FDA review later this year."

PGDx's MSI testing is incorporated in the company's tissue-based CancerSELECT 125 pan cancer genomic profiling assay and its non-invasive PlasmaSELECT 64 pan cancer assay that analyzes circulating tumor DNA in patient plasma. The company also recently received grant funding from the National Cancer Institute to advance liquid biopsy tests for determining a related biomarker known as tumor mutational burden.

PGDx was an early leader in identifying the importance of MSI, contributing to a study on MMR and immune checkpoint blockade presented at the 2015 ASCO Annual Meeting. In that study, researchers found that colorectal cancer patients who had tumors with MSI/MMR deficiency had a much greater therapeutic response to pembrolizumab. The analysis showed that cancer patients with MSI/MMR deficiency on average had more than 20 times the number of mutations in their tumors as similar patients who were not mismatch repair deficient. This finding is consistent with other studies showing that PD-1/PD-L1 checkpoint blockers are most effective against tumors containing many mutations. The study was published in the New England Journal of Medicine.

"We established PGDx to advance technology invented at Johns Hopkins based on our belief that greater understanding of tumor genomics would ultimately enable more effective and less toxic treatments for cancer," noted Victor E. Velculescu, MD, PhD, a co-founder of PGDx. Dr. Velculescu also is Professor of Oncology at the Johns Hopkins University School of Medicine. "This breakthrough approval from the FDA is an important milestone in the realization of that vision. I am proud that PGDx has played a significant role in this advance and that the company will help many more patients realize the benefits of immuno-oncology approaches for cancer treatment."

PGDx representatives will be attending the 2017 ASCO Annual Meeting and are available at Booth #2078 to discuss the company's MSI testing and its complete range of cancer genome analysis tools for researchers and clinicians. Research services include exome and targeted approaches for tissue specimens, targeted approaches for plasma samples and a variety of custom tissue and plasma-based options designed to address the specific research needs of cancer researchers and drug developers. PGDx's service offerings for researchers and testing labs are complemented by the clinical services it provides to patients and physicians through its CLIA-certified laboratory, including its CancerSELECT 125 pan cancer genomic profiling assay and the non-invasive PlasmaSELECT 64 pan cancer profiling assay, both of which include MSI testing.

About Personal Genome DiagnosticsPersonal Genome Diagnostics (PGDx) is empowering the fight against cancer by unlocking actionable information from the genome for oncology researchers, drug developers, clinicians and patients. The expert team at PGDx draws on a deep understanding of cancer biology, extensive experience in cancer genomics and clinical oncology, and the company's distinctive technologies that precisely identify and characterize unique genomic alterations in tumors. PGDx is working toward broad patient access to its genomic technologies and products, through a CLIA-certified facility providing comprehensive genomic services, as well as a portfolio of tissue-based and liquid biopsy genomic testing products for laboratories worldwide. Privately-held PGDx is headquartered in Baltimore, MD. For additional information, visit PersonalGenome.com.

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http://PersonalGenome.com

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Personal Genome Diagnostics Highlights its Patent-Pending Microsatellite Instability Testing Technology as FDA ... - PR Newswire (press release)

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