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Many of the fundamental features of life don’t necessarily have to be the way they are. Chance plays a major role in evolution, and there are always alternate paths that were never explored, simply because whatever evolved previously happened to be good enough. One instance of this idea is the genetic code, which converts the information carried by our DNA into the specific sequence of amino acids that form proteins. There are scores of potential amino acids, many of which can form spontaneously, but most life uses a genetic code that relies on just 20 of them.

Over the past couple of decades, scientists have shown that it doesn’t have to be that way. If you supply bacteria with the right enzyme and an alternative amino acid, they can use it. But bacteria won’t use the enzyme and amino acid very efficiently, as all the existing genetic code slots are already in use.

In a new work, researchers have managed to edit bacteria’s genetic code to free up a few new slots. They then filled those slots with unnatural amino acids, allowing the bacteria to produce proteins that would never be found in nature. One side effect of the reprogramming? No viruses could replicate in the modified bacteria.

Radiation therapy was first used to treat cancer more than 100 years ago. About half of all cancer patients still receive it at some point during their treatment. And until recently, most radiation therapy was given much as it was 100 years ago, by delivering beams of radiation from outside the body to kill tumors inside the body.

Though effective, external radiation can also cause collateral damage. Even with modern radiation therapy equipment, “you have to [hit] normal tissue to get to a tumor,” said Charles Kunos, M.D., Ph.D., of NCI’s Cancer Therapy Evaluation Program (CTEP). The resulting side effects of radiation therapy depend on the area of the body treated but can include loss of taste, skin changes, hair loss, diarrhea, and sexual problems.

Now, researchers are developing a new class of drugs called radiopharmaceuticals, which deliver radiation therapy directly and specifically to cancer cells. The last several years have seen an explosion of research and clinical trials testing new

Scientists created a synthetic genome for a bacterium by stringing together building blocks of DNA — and the new genome made the microbe immune to viral infection.

Even when exposed to a cocktail of bacteriophages — viruses that infect bacteria — the designer Escherichia coli remained unscathed, while an unmodified version of the bacterium quickly succumbed to the viral attack and died, the research team reported in their new study, published Thursday (June 3) in the journal Science. That’s because viruses usually hijack a cell’s internal machinery to make new copies of themselves, but in the designer E. coli, that machinery no longer existed.

When Open AI’s GPT-3 model made its debut in May of 2020, its performance was widely considered to be the literal state of the art. Capable of generating text indiscernible from human-crafted prose, GPT-3 set a new standard in deep learning. But oh what a difference a year makes. Researchers from the Beijing Academy of Artificial Intelligence announced on Tuesday the release of their own generative deep learning model, Wu Dao, a mammoth AI seemingly capable of doing everything GPT-3 can do, and more.

First off, Wu Dao is flat out enormous. It’s been trained on 1.75 trillion parameters (essentially, the model’s self-selected coefficients) which is a full ten times larger than the 175 billion GPT-3 was trained on and 150 billion parameters larger than Google’s Switch Transformers.

In order to train a model on this many parameters and do so quickly — Wu Dao 2.0 arrived just three months after version 1.0’s release in March — the BAAI researchers first developed an open-source learning system akin to Google’s Mixture of Experts, dubbed FastMoE. This system, which is operable on PyTorch, enabled the model to be trained both on clusters of supercomputers and conventional GPUs. This gave FastMoE more flexibility than Google’s system since FastMoE doesn’t require proprietary hardware like Google’s TPUs and can therefore run on off-the-shelf hardware — supercomputing clusters notwithstanding.

But the above-ground structure of the Baekdu-daegan Seed Vault belies the true size of this sprawling underground structure.

The idea of building a Seed Vault in South Korea initially began with the Nagoya Protocol on Access and Benefit Sharing in 2010. Officially launched in 2016 and designated a national security facility since 2019, the Baekdu-daegan Seed Vault’s main purpose is to secure biodiversity from threats such as natural disasters, climate change and war, to support sustainable life for human beings.

The Baekdu-daegan Seed Vault in Korea is one of only two built worldwide — the other is Svalbard Global Seed Vault, which opened in 2008 on an arctic Norwegian Island. It currently stores over 90000 types of seeds.

REvil threat actors may be behind a set of PowerShell scripts developed for encryption and weaponized to exploit vulnerabilities in corporate networks, the ransom note suggests.

Threat actors have deployed new ransomware on the back of a set of PowerShell scripts developed for making encryption, exploiting flaws in unpatched Exchange Servers to attack the corporate network, according to recent research.

Researchers from security firm Sophos detected the new ransomware, called Epsilon Red, in an investigation of an attack on a U.S.-based company in the hospitality sector, Sophos Principal Researcher Andrew Brandt wrote in a report published online.

This is a technological triumph.


Twenty-one years ago, researchers announced the first “draft” of sequencing the complete human genome. It was a monumental achievement, but the sequence was still missing about 8 percent of the genome. Now, scientists working together around the world say they’ve finally filled in that reclusive 8 percent.

If their work holds up to peer review and it turns out they really did sequence and assemble the human genome in its entirety, gaps and all, it could change the future of medicine.

Two missions will study the hellish planet to piece together its climate past, look for volcanoes, and see if it was ever habitable.


NASA Administrator and former astronaut Senator Bill Nelson announced today that the agency would be sending two missions to Venus. The two missions, called DAVINCI+ and VERITAS, will respectively study the planet’s atmosphere and geological history.

“These two sister missions both aim to understand how Venus became an inferno-like world capable of melting lead at the surface,” Nelson said during his State of NASA address. “They will offer the entire science community the chance to investigate a planet we haven’t been to in more than 30 years.”