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Tiếp tục đọc Những Ngày Đầu Tiên Đến Nước Mỹ 08/03/2007(Xem: 150866) Phùng Văn Phụng Tác giả Phùng văn Phụng, định cư tại Mỹ theo diện HO đã13 năm.

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Let's not complicate things: Live life fully, fruitfully and peacefully. First I would to thank God for getting me where I am today.

(Jul 04) [Independence Day] A 27-year-old who worked for Apple as a teenager wants to make a yearly blood test to diagnose cancer — and he just got .5 million from Silicon Valley VCs to pull it off (This portrait was taken a while ago ... What really counts is not when you explain for the first time something like Fracto Gene; "Fractal Genome Grows Fractal Organisms".

Yes, there are countries (including a sub-Continent) trying to gain access to the IP, in order to get the green to the US oncogenomics market. Yes, since another genomic phenomenon was also visible (by the naked eye in Indian Corn) - but her breakthrough had to wait about 40 years.

15 is better than 40 - and I am younger (though not by much...) than she was to see a breakthrough actually unfolding.

- holgentech_at_gmail_dot_com) Big Pharma & Big IT might lead together Genome Business by means of Genome Editing to cure cancers (Facebook note by Andras Pellionisz) Once upon a time, there was the Axiom that "Atoms Do Not Split”.

When they did, nuclear technology emerged prompted by the fact that fission (or fusion) releases unheard amounts of energy. First, however, quantum physics had to be developed to understand and thus control the process.

But a new wave of research, exemplified by a study published in Nature Genetics by a team at Cold Spring Harbor Laboratory (CSHL), is significantly improving our ability to target cancer cells by studying "the other 98%" of DNA in human chromosomes, sometimes called the genome's "dark matter." Research led by Michael Feigin, Ph.changes with epigenomics, mutations, etc.), "Genome Editing" Researchers looked at cells sampled from 308 people with pancreatic cancer, finding mutations in gene promoter regions that provide important clues about pathways perturbed in the illness and suggesting new targets for future treatments.Over the last decade, it has made good sense to study the genetic drivers of cancer by sequencing a tiny portion of the human genome called the exome -- the 2% of our three billion base pairs that "spell out" the 21,000 genes in our chromosomes.just like my - too early - original Google Tech Talk You Tube was recorded in 58 minutes 9 years ago in 2008. At the time of inception (2002, that is, 15 years ago) it was predicted at the outset that the breakthrough of reversing both mistaken axioms of Genomics (the Junk DNA and Central Dogma misnomers) would not be accepted very quickly - though the peer-reviewed science paper "Principle of Recursive Genome Function" appeared almost at the minute when the establishment admitted with ENCODE that "the community of scientists have to re-think long held beliefs".Now, after nearly a decade, it is compressed by Dr. Self-similar repeats in the DNA are visible in the billions of A, C, T, G-s (it is hopeless to try not to repeat sequences if you can only use 4 letters to write a very long book) ...The utility lies in the statistical correlation and probabilistic prediction of cause-and-effect of two fractal sets.