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From: Paul H. Christiansen2/7/2020 1:03:31 PM
   of 992
 
Could Photonic Chips Outpace the Fastest Supercomputers

There’s been a lot of talk about quantum computers being able to solve far more complex problems than conventional supercomputers. The authors of a new paper say they’re on the path to showing an optical computer can do so, too.

The idea of using light to carry out computing has a long pedigree, and it has gained traction in recent years with the advent of silicon photonics, which makes it possible to build optical circuits using the same underlying technology used for electronics. The technology shows particular promise for accelerating deep learning, and is being actively pursued by Intel and a number of startups.

Now Chinese researchers have put a photonic chip to work tackling a fiendishly complex computer science challenge called the subset sum problem in a paper in Science Advances. It has some potential applications in cryptography and resource allocation, but primarily it’s used as a benchmark to test the limits of computing.

Read More – Singularity Hub


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From: Paul H. Christiansen2/7/2020 1:12:34 PM
1 Recommendation   of 992
 
Alphabet Has a Second, Secretive Quantum Computing Team

In October, Google celebrated a breakthrough that CEO Sundar Pichai likened to the Wright brothers’ first flight. Company researchers in Santa Barbara, California, 300 miles from the Googleplex, had achieved quantum supremacy—the moment that a quantum computer performs a calculation impossible for any conventional computer.

That was both notable science and a chance for Google to show prominence in a contest among big tech companies, including IBM and Microsoft, to deliver the wild new power promised by quantum computing. The usually low-profile Pichai threw himself into marking the moment, penning a blog post, taking part in a rare media interview, and posting an Instagram photo of himself alongside the shiny machine that scored the result.

Read More - Wired

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From: Paul H. Christiansen2/11/2020 3:12:24 PM
   of 992
 
Arm Brings AI and Machine Learning to IoT and the Edge

For a company that doesn’t manufacture anything, Arm has a surprisingly large and broad impact, not only on the chip industry, but the overall tech industry and, increasingly, many other vertical industries as well.

The company—which creates semiconductor chip designs that it licenses as IP (intellectual property) and then Arm’s customers use the designs to build chips—is the brains behind virtually every smartphone ever made. In addition, it has a small but growing market in data center and other network infrastructure equipment and is the long-time leader in intelligent devices of various types—from toys to cars and nearly everything in between; essentially the “things” part of IoT (Internet of Things).

Read More $ Tech.pinions

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From: Paul H. Christiansen2/11/2020 3:28:28 PM
   of 992
 
AI-formulated medicine to be tested on humans for the first time

A drug designed entirely by artificial intelligence is about to enter clinical human trials for the first time. The drug, which is intended to treat obsessive-compulsive disorder, was discovered using AI systems from Oxford-based biotech company Exscientia. While it would usually take around four and a half years to get a drug to this stage of development, Exscientia says that by using the AI tools it's taken less than 12 months.

The drug, known as DSP-1181, was created by using algorithms to sift through potential compounds, checking them against a huge database of parameters, including a patient's genetic factors. Speaking to the BBC, Exscientia chief executive Professor Andrew Hopkins described the trials as a "key milestone in drug discovery" and noted that there are "billions" of decisions needed to find the right molecules for a drug, making their eventual creation a "huge decision." With AI, however, "the beauty of the algorithm is that they are agnostic, so can be applied to any disease."

Read More - Engadget

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From: Paul H. Christiansen2/11/2020 3:33:49 PM
   of 992
 
Cloud data platform giant Snowflake raises $479M at $12.4B valuation, partners with Salesforce

Data warehousing startup Snowflake Computing announced a $479 million funding round that gives the cloud company a whopping $12.4 billion valuation.

Dragoneer Investment Group — a backer of Airbnb, Slack, Spotify, Uber and other giants — led the Series G round and Salesforce Ventures participated for the first time. Snowflake also announced a new partnership with Salesforce; details of that deal will be announced in June.

Read More - GeekWire

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From: Paul H. Christiansen2/11/2020 3:38:53 PM
   of 992
 
Here are Disney’s hurdles in becoming an international streaming sensation

Walt Disney Co. breezed past analysts’ estimates for its new Disney+ streaming service, which was unveiled in November.

Still, there are a few hurdles that remain before Disney DIS, -1.16% can be considered a global sensation. The Burbank, Calif.-based company may be the world’s most recognized media brand, but it’s not immune to the challenges of the over-the-top (OTT) television environment, especially for subscription video on demand (SVOD).

Chief Executive Officer Robert Iger, in the first earnings report since the company released Disney+, said Tuesday it got 26.5 million subscribers through the end of December. Growth continued in the current quarter, with another 2 million subscribers added, bringing the total to 28.6 million. To put that number in perspective, Hulu recently passed 30 million subscribers despite launching 12 years ago.

Read More Market Watch

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From: Paul H. Christiansen2/11/2020 3:47:21 PM
   of 992
 
Five Takeaways From the FTC’s New Antitrust Probe

Much of the antitrust scrutiny on big tech companies has focused on whether their biggest acquisitions violated competition laws. Now the Federal Trade Commission, in a sweeping review of five iconic players in the industry, is looking at whether their smaller deals might have hurt competition, too.

On Tuesday, the FTC said it has ordered the five companies—including Apple, Facebook, Amazon, Microsoft and Alphabet, the parent company of Google—to provide details and documents about the acquisitions they completed between the beginning of 2010 and the end of 2019. The agency is looking strictly at deals that the companies didn’t previously report to antitrust regulators under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, a federal law that requires companies to file details about proposed mergers that meet certain requirements.

Here are five takeaways from the FTC’s announcement:

Read More - $ The Information


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From: Paul H. Christiansen2/12/2020 10:06:49 AM
   of 992
 
Preparing for a Digital Transformation in Manufacturing

Most CEOs understand they are in a race to implement artificial intelligence

Last year, the Association for Advancing Automation (A3) surveyed our members about their companies’ adoption of AI. More than 76% of respondents felt that AI will be important to their companies in the next 3 years. However, just 3.3% of those surveyed said that AI was being widely applied in their organizations.

This has been called the Ambition-Execution Gap.

Companies know they need to implement AI strategies but are frequently at a loss on where to begin. Or they get stuck in a pilot purgatory where AI initiatives never reach a scale where they can help the overall enterprise. Even when on the right track, there’s not the talent in the pipeline to support their efforts.

Read More – Association for Advancing Automation

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From: Paul H. Christiansen2/13/2020 3:26:49 PM
   of 992
 
PolarityTE Announces Pricing of Public Offering of Common Stock and Warrants

Has the subsequent selloff been irrational?

On Tuesday of this week PTE made the above announcement after the market closed. On Wednesday, PTE opened at $1.75 per share, down 45% from the previous day’s close. For the day, more than 7 million shares traded, almost all within a small variance of $1.70 per share.

The sell-off was probably expected: traditional Wall Street thinking dictates that investors should sell whenever existing shares are exposed to dilution.

However, one has to wonder if those selling their shares bothered to read the following - Our Vision – which is taken verbatim from a separate registration statement filed with the SEC and which will be included in the final Prospectus.

The section Where You Can Find More Information offers instructions on how to obtain that information.

Here is PTE’s Our Vision:



We aspire to be a global biotechnology company that provides superior, tangible, and pragmatic platform technologies that provide superior results to patients, while reducing costs and promoting improved health economics for patients, providers, and payors. We believe this can be accomplished through our pursuit of complex simplicity, which embodies the development of robust cell/tissue-derived therapies that can be efficiently produced and deployed. PolarityTE is committed to delivering transformative technology that positively impacts humanity.

PolarityTE was founded by a dedicated group of doctors and scientists from The Johns Hopkins University School of Medicine, who left to become part of something bigger. Something that could transform the future of medicine. We believe that living systems require more than a simple singular input (for example a growth factor, stem cell, or nano-particle), to produce a complex output. Therefore, we took a different direction and developed multi-tiered platform technologies that propagate the necessary complex substrate required for regenerating fully-functional tissue, such as skin, bone, cartilage, muscle, blood vessels, and neural elements, as well as solid and hollow organ composite tissue systems. We have engineered and developed our regenerative materials and core tissue substrate technology platforms to allow us to induce, maintain, and promote the integrated polarity, organized assembly, and interface development of cells and tissues, so that they replicate regenerative healing in the body and are not seen as foreign by the immune system.

The core technology of TE products is minimally polarized functional units (“MPFUs”) consisting of self-complexing intelligent regenerative materials (“SCIRM”). SCIRM within an MPFU form polarizing, multi-cellular aggregates that act as an intrinsic, regenerative bio-reactor capable of expanding, proliferating, and synthesizing cells, materials, factors, or systems necessary for regenerating full-thickness, three-dimensional tissue. The TE products we develop begin with the patient’s own tissue to produce SCIRM that address the specific tissue or system needed for the patient’s care. Our product pipeline focuses on the development of regenerative products for a variety of tissue types and organ systems that are commonly altered, injured, or destroyed by a variety of diseases, pathologies, traumatic events, and medical interventions.

SkinTE, our first tissue product, was registered with the United States Food and Drug Administration (FDA) in August 2017, and is now commercially available for the repair, reconstruction, replacement, and regeneration of skin in patients who have a need for treatment of acute or chronic wounds, burns, surgical reconstruction events, scar revision, or removal of dysfunctional skin grafts. We are pursuing a regional plan for commercial rollout that began in late October 2018, and at the beginning of January 2019 we had 24 sales representatives in the field marketing SkinTE.

OsteoTE is designed to utilize the patient’s bone to repair, reconstruct, replace, supplement, or regenerate bone damage or defects. We registered OsteoTE with the FDA in December 2018. We are preparing for the first application of the product in a clinical setting, which we are endeavoring to achieve in the first half of 2019.



Human cells, tissues and cellular and tissue-based products (“HCT/Ps”) are governed by specific FDA regulations that provide for a registration pathway that is different than the pathway for traditional drug candidates. SkinTE and OsteoTE are both registered as HCT/Ps under Section 361 of the Public Health Service Act.

We have a number of additional TE products under development, including the following:

· AdipoTE to optimize the delivery of autologous fat beyond the capabilities of current fat transfer techniques utilized in procedures on, among others, the breast, buttocks, and face;

· AngioTE to address vascular regeneration including microscopic capillary networks all the way up to great vessel replacement;

· NeuralTE for peripheral nerve injuries of the extremities, as well as for patients with neuromas or chronic compression due to joint replacements, migraines, craniofacial injuries, carpal tunnel syndrome, and those who have undergone hernia or abdominal-based procedures;

· UroTE targeting the delivery of autologous urogenital epithelium and submucosa across a spectrum of diseases and processes, including urethral strictures, urethral creation, bladder reconstruction, and ureter reconstruction;

· LiverTE to address numerous causes of liver failure, including NASH, fibrosis/cirrhosis, surgical resection of the liver; and

· BowelTE to deliver an optimized autologous construct to aid in the regeneration of bowel tissue.

RTD and ARC represent research and development of new science and product opportunities based on what we learned while developing the TE platform. RTD is focused on altered state analytes for the generation of composite materials that can be utilized for the augmentation, modulation, and regulation of cell and tissue-derived systems. ARC is focused on the design and development of gene transfer, small molecule synthesis, composite therapeutics, and alteration of self-propagating cell/tissue-derived bioreactors.

We have significant research facilities and a well-educated and skilled team of scientists and researchers. These resources are highly beneficial to the work we are doing on our TE products and in RTD and ARC. We also offer research services to unrelated third parties on a contract basis, which we offer under the trademark POLARITYRD. Contract research services help us defray the costs of maintaining a first-rate research facility and allow us to meet companies pursuing new technologies that may be opportunities for collaborative or strategic relationships going forward.

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From: Paul H. Christiansen2/14/2020 12:13:53 PM
1 Recommendation   of 992
 
Crispr'd Cells Show Promise in First US Human Safety Trial

It’s been over three years since US regulators greenlit the nation’s first in-human test of Crispr’s disease-fighting potential, more than three years of waiting to find out if the much-hyped gene-editing technique could be safely used to beat back tough-to-treat cancers. Today, researchers from the University of Pennsylvania and Stanford finally revealed the first published report describing the trial. The highly anticipated results showed that the procedure is both safe and feasible; the Crispr’d cells went where they were supposed to go and survived for longer than expected. They didn’t cure anyone’s cancer, but they didn’t kill anyone, either, which means the results hold significant promise for the future of Crispr-based medicines.

Read More - Wired

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