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Category Archives: Transhuman News

Jesse Matthew DNA examined in 2013 missing teen’s case – Video

Posted: October 24, 2014 at 6:50 pm


Jesse Matthew DNA examined in 2013 missing teen #39;s case
The Hannah Graham investigation has prompted investigators in Nelson County, Virginia to look further into the 2013 disappearance of 17-year-old Alexis Murphy.

By: USA TODAY

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DNA Evidence Links Guthrie Man To Decade-Old Sexual Assault

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GUTHRIE, Oklahoma -

A Guthrie man was arrested this week after DNA evidence linked him to a 16-year-old sexual assault that was nearly past the statute of limitations.

Agents with the Oklahoma State Bureau of Investigation (OSBI) arrested 35-year-old David Jerome Stephens II on Wednesday, after a DNA analyst alerted the bureau of a positive hit in the Combined DNA Index System.

The alleged crime occurred on Christmas Day in 1997. The victim, an 85-year-old woman, was beaten with a pipe, robbed and sexually assaulted. The victim passed away in 2008.

The positive hit in the DNA index system happened just days before the statute of limitations for the crime would have run out. Luckily, the OSBI agent was able to file a John Doe warrant based on the new DNA evidence, which allowed the case to remain legally active.

Stephens was arrested Wednesday evening at his home in the 11700 block of Red Cedar Rd. in Guthrie. DNA from Stephens was collected after a conviction in 2013 for Possession of a Controlled Dangerous Substance within 1,000 feet of a School/Park/Child.

Stephens was booked into the Logan County Jail. Details on a possible bond were not available. According to the OSBI, Stephens has a lengthy arrest record beginning in 1997, the same year as the alleged sexual assault. He would have been 20 years old at that time.

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DNA Evidence Links Guthrie Man To Decade-Old Sexual Assault

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[MINUSmin31] Sebastian Mullaert & Patrick Siech – Genome I – Video

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[MINUSmin31] Sebastian Mullaert Patrick Siech - Genome I
Sebastian Mullaert Patrick Siech Announce Part One of Their Genome Trilogy Inspired in equal measure by analog synthesizer technology and the lush Swedish countryside, Genome marks the...

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[MINUSmin31] Sebastian Mullaert & Patrick Siech - Genome I - Video

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Edico Genome Announces Launch of Dragen Processor

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Edico Genome Inc., a San Diego-based company that makes integrated circuits for processing genomic data, announced the broad commercial launch of its flagship Dragen processor.

Dragen is a chip that users can integrate into their servers or sequencing instruments to map sequencing reads, or DNA fragments, to a reference genome. The idea is that the chip can help companies piece short reads together to create a complete genome. This is a much faster approach than using a general purpose server, and it relieves one of the most time-consuming steps in working with genomic data.

Edico has recently grown from eight employees to 24, and made its first sale of the Dragen chip last month to San Diego-based Sequenom Inc., a prenatal testing company. Sequenom generated 20 million short reads on a sequencing machine to identify fetal chromosomal disorders from maternal blood samples. The reads were then mapped using both the Dragen chip and a standard pipeline that included Bowtie 2 as the mapping algorithm. Sequenom reported that the Dragen processor mapped the entire set of reads in nine seconds, roughly 30 times faster than the standard pipeline, with no significant difference in sensitivity or specificity in detecting the indicators that help determine fetal genetic disorders.

The impact of Dragens ability to rapidly and accurately analyze data in a cost-effective manner is greatly magnified when analyzing massive data sets, such as whole genomes, or large numbers of smaller tests such as RNA sequencing, said Pieter van Rooyen, chief executive officer of Edico Genome. Due to these advantages, weve already had a tremendous response to Dragens early access program, and now we are able to make our bio-IT processor broadly available to companies and academic institutions with low to very high-volume sequencing capacities.

The company sees particular benefits for using Dragen for cancer treatment, non-invasive prenatal testing and diagnosing rare disease, he added.

Edico has also announced that a Dragen processor is now deployed at the San Diego Supercomputer Center, which serves university and nonprofit labs across the city.

The company is headquartered at the EvoNexus incubator in La Jolla, and raised $10 million in venture capital earlier this year to commercialize the chip.

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Pacific Biosciences of California Earnings Rocket Higher on Roche Deal

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There are two types of companies when it comes to sequencing human genomes: Illumina and everyone else. While Pacific Biosciences of California failed on its promise and hype in 2010 to revolutionize human genome sequencing, it has carved out a spectacular niche and built an envious reputation when it comes to sequencing microbial genomes with ultrahigh accuracy. Good news: high-quality microbial genomes are becoming increasingly more important in commercial applications and Pacific Biosciences is gradually developing additional business opportunities as it expands its capabilities.

The genomic diagnostics partnership signed with Roche in September 2013 is a prime example of management's vision to diversify the business -- and it has certainly catalyzed share gains for investors.

PACB data by YCharts

Yet, while encouraged by the progress and commitment from a blue chip biotech company, investors are also curious about the path to profitability. Do the recent Pacific Biosciences earnings provide any clues? Here's what you need to know.

By the numbers Pacific Biosciences had a great quarter for two reasons. First, it realized $11.7 million in revenue from the Roche partnership: $10 million from hitting a milestone and $1.7 million in quarterly amortization of the upfront payment. Second, it grew product revenue 15.6% and service revenue 34.7%. The company booked 16 orders of its third-generation DNA sequencing system, the PacBio RS II, and has now booked 30 systems year to date. That compares favorably to the 16 bookings made through the first three quarters last year and should keep the momentum going.

3Q14

3Q13

% Change

Product Revenue

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Trailer – EczemaHelp – Video

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Trailer - EczemaHelp
Vous avez de l #39;eczma atopique ? Notre objectif vaincre l #39;eczma ensemble ! Partagez votre exprience avec notre communaut. Dcouvrez de nombreux conseils et modes de vie pour une...

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Home remedy for eczema – Beat eczema – Video

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Home remedy for eczema - Beat eczema
Click here - http://bit.ly/1xdbleU Home remedy for eczema - Beat eczema If you have the desire to live without eczema #39;s dry, sensitive skin and you have the drive to do something about...

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Diabetic foot, Psoriasis, mood disorder – Remedy Hospital in Hyderabad – 6TV Sanjeevani – Video

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Diabetic foot, Psoriasis, mood disorder - Remedy Hospital in Hyderabad - 6TV Sanjeevani
6TV Sanjeevani is a special program to create awareness on diseases which leads to health problems disturbing daily life. The safety measures, remedies to be taken for the diseases and the...

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Diabetic foot, Psoriasis, mood disorder - Remedy Hospital in Hyderabad - 6TV Sanjeevani - Video

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Gene scan helps diagnose mystery disorders in children

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(HealthDay News) -- A new test that scans all of a person's genes to pinpoint a single mutation can help identify rare genetic disorders in children, a new study shows.

Audrey Lapidus and her husband grew concerned when their son Calvin didn't roll over or crawl by the time he was 10 months old. He also had chronic digestive problems. A series of tests didn't provide any answers.

In desperation, Calvin's parents agreed to have their son become the first person to undergo a powerful new test called exome sequencing at the University of California, Los Angeles.

DNA from Calvin and his parents was placed in a machine that rapidly scanned and compared the three family members' genomes. The machine identified a mutation on the boy's 18th chromosome. He was diagnosed with Pitt-Hopkins Syndrome, a rare genetic disorder that affects only 250 children worldwide, according to researchers.

The diagnosis meant that Calvin's parents could start seeking the best treatment for their son, according to the study published online Oct. 18 in the Journal of the American Medical Association.

"Our study is the first to show that sequencing a child's genome together with his or her parents' dramatically improves geneticists' ability to reach a firm diagnosis in rare disorders," corresponding author Dr. Stan Nelson, vice chair of human genetics and a professor of pathology and laboratory medicine at David Geffen School of Medicine at UCLA, said in a university news release.

Calvin was the first of more than 800 children included in the study.

"We discovered a genetic cause for the conditions affecting 40 percent of the hundreds of young children who come to UCLA for exome sequencing due to developmental delays or intellectual disabilities," Nelson said.

The findings make a strong case for routine clinical use of exome sequencing in efforts to diagnose children with rare genetic disorders, the researchers said.

Unlike earlier tests that assess one gene at a time, exome sequencing rapidly surveys all of a person's 20,000 genes in order to identify a single mutation. The test focuses on the exome, which are protein-encoding parts of genes that account for only 1 percent of DNA but nearly 85 percent of errors known to cause diseases.

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Three UCSF Faculty Elected to Institute of Medicine

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Three UCSF faculty members are among 70 new members and 10 foreign associates of the Institute of Medicine (IOM) announced during the organizations 44th annual meeting announced on Oct. 20.

Eric P. Goosby, MD, professor of medicine and director of the Institute of Global Health Delivery and Diplomacy; Deepak Srivastava, MD, professor of medicine and director of the Gladstone Institute of Cardiovascular Disease; and Ron Vale, PhD, professor of cellular and molecular pharmacology and Howard Hughes Medical Institute investigator are the latest UCSF members, bringing the total number of IOM members elected from UCSF to 92.

These individuals and all UCSF members of the Institute of Medicine represent the breadth of our expertise, ranging from national and international leadership in public health to explorations into the genetic blueprint and smallest functional molecules, saidBruce Wintroub, MD, interim dean of the UCSF School of Medicine. Each of them has greatly contributed to our knowledge of disease and our advancement of human health. I congratulate Doctors Goosby, Srivastava and Vale for their extraordinary accomplishments, and I am grateful that they are part of the UCSF community.

Eric P. Goosby, MD

Goosby has a long career in international HIV/AIDS. He was the CEO and chief medical officer of Pangea Global AIDS Foundation from 2001 to 2009, and previously was the director of National AIDS Policy at the While House under President Clinton and the director of the Ryan White Care Act at the US Department of Health & Human Services.

In his role as the Global AIDS Ambassador, Goosby was the nations senior global health diplomat, advancing the mission to improve and save lives and to foster global sustainability. He oversaw PEPFAR (the Presidents Emergency Plan For AIDS Relief), the largest public health endeavor in history with over $45 billion invested in 10 years.

Deepak Srivastava, MD

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Three UCSF Faculty Elected to Institute of Medicine

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