Wave Genome LLC has developed a groundbreaking technology which allows nonlocal control of Wave Optics of chromosomes in order to focus genetic bioholographic information for rejuvenation therapies at the level of DNA.
WVE-006, its alpha-1 antitrypsin deficiency (AATD) candidate, completed its Phase I clinical trial successfully and demonstrated proof of concept.
Bioholographic Remote Stem Cell Therapy
Stem cells play an essential role in human body development due to their remarkable capabilities of self-renewal and differentiation into specific cell types. Their incredible self-renewal potential makes them an excellent candidate for regenerative medicine; however, fully developed cell therapies are still several years away due to multiple hurdles such as cultivation time-consuming cultivation processes for stem cells as well as inducing specific cell differentiation processes.
Researchers are turning to artificial intelligence (AI) as a solution, using it to analyse large datasets and increase efficiency during stem cell research. AI algorithms are adept at processing biological data, recognizing patterns and making predictions based on image features; in addition they help optimize cell cultures as well as predict which cell type will best benefit each individual patient.
AI has quickly become a valuable tool in both regenerative medicine and drug discovery. It is capable of screening large compound databases, identifying molecular structures and properties of candidate drugs against specific diseases, as well as evaluating efficacy. AI is often employed for stem cell analysis to detect images and predict their morphological properties.
WAVE GENOME LLC’s new Wave Genomic Technology brings together cutting-edge advances in computational and biochemical science to produce “lenses” that assist our chromosomes in correcting their refraction, thus focusing genetic Bioholographic information both locally and remotely. This is made possible via Quantum Nonlocality of an Embryonic Stem Cell Wave Matrix which enables remote management of biosystem via its holographic signal.
Utilizing its technology, the company was able to increase circulating wild-type AAT protein levels in patients with homozygous AATD to levels sufficient for regulatory approval of weekly IV augmentation therapy – the first results of their kind that could potentially improve patient treatment outcomes in those living with AATD.
Future goals of the company include using its holographic technology for other clinical trials, such as improving iPSC differentiation and predicting regenerative therapy effectiveness. Furthermore, they aim to develop an in vivo model of aging and dementia to aid with designing more effective treatments while creating a healthier society.
Electret Excitation
An electret is a piece of dielectric material with a permanent electric charge that generates internal and external electric fields – functioning similarly to permanent magnets in terms of electrostatics. They can be charged using external electric fields, holding their charges depending on temperature and exposure time for prolonged periods.
Electrets can be used to monitor and record the electrical activity of cells. While commonly seen in microphones and cell phones, electrets have many applications in biology as well – including modulating embryonic stem cell regeneration capabilities using electrets.
At the outset of creating an electret is charging material: Teflon (polytetrafluoroethylene or PTFE) makes an ideal material and can be purchased affordably at stores like Grainger or Zoro in sheets with various thicknesses and prices. An electrostatic field meter such as Monroe Electronics’ model 256 or Prostat PFM-711A can then be used to determine its electrostatic potential and measure it accordingly.
Corona discharge is commonly used to charge polymer films, with one proposal suggesting that corona-charged PTFE polymers may carry charges carried by electrons or ions deposited on their surface. Unfortunately, however, its exact nature remains unanswered.
To further our understanding of polymer charging mechanisms, we conducted experiments comparing the kinetics of tribocharging and corona charging as well as electrostatic charges on different types of uniaxial and uniaxially oriented PTFE polymer samples.
Our results showed that PTFE electrets prepared through both tribocharging and corona charging had the same initial surface potential, although corona-charged polymers lost charge more slowly over time than their tribocharged counterparts. This finding supports our hypothesis that its initial surface charge is due mainly to corona discharge-deposited ions on its polymer surface; our findings also suggested that the polarizable charge equilibrium (PCE) method accurately measures persistence length (LP).
Quantum Biononlocality
Quantum Biononlocality refers to the ability to program nonlocal signals instantly. This concept forms the core of Quantum Remote Stem Cell Therapy, in which laser reprogramming of embryonic stem cell wave matrix can correct genetic mutations within an individual’s body safely and effectively without the use of chemicals; furthermore it’s also wireless and tailored directly towards your cells delivering energy directly for healing.
Quantum theory allows for nonlocality; however, experimental proof remains controversial. Results from delayed choice experiments do not make sense from the perspective of local realism; however, they align perfectly with principles of nonlocality as encapsulated by Bohr-causality and space-time symmetries that underlie quantum mechanics.
As the universe is a hologram, every point in it is uniquely encoded with information that can be accessed via DNA’s wave matrix and genome sequence. Through their genetic information and zero center (Quantum Nonlocality), each person possesses their own personal map of Quantum Nonlocality that represents them uniquely.
Evidence of this was evident in the epigenetic profiles and promoter architecture features of miR-430 cluster genes and other minor wave genes during early development. Publicly available epigenomic datasets on ATAC-seq (Assay for Transposase-Accessible Chromatin) and ChIP-seq regulation correlated to gene expression levels; open chromatin displayed the highest promoter activity level. At the 256-cell stage, minor wave genes had higher and broader H3K27ac signals than major wave genes. This may reflect differences in activation mechanisms at and post MBT as well as differences between promoter sequences or DNA methylation patterns. Minor wave genes were more similar to the CG set than major wave genes; however, differences were less prominent during post-gastrulation stages. This implies that transcription body formation is driven by an epigenetic mechanism and therefore, early formation of transcriptional complex may increase chances for formation of minor wave gene cluster.
Quantum Leap
A quantum leap is a moment of profound change, where your life changes drastically as you transition from old habits and routines to something completely different. A quantum leap offers you an opportunity to shape the reality that surrounds you by manifesting your dreams into existence – it can transform your entire world! Achieve your goals faster!
Thirty years have passed since Dr. Sam Beckett entered the Quantum Leap accelerator and disappeared, and now scientists are using that same technology to attempt to understand its mysteries. Their hopes may be high but their results don’t meet them expectations. At the helm of their team is Ben Song – an experienced Army veteran with impeccable scientific acumen who brings steady precision and accuracy to this project aided by Addison (a hologram only Ben can see and hear).
The quantum leap is a quantum mechanical effect caused by the entanglement between multiple particles such as photons, electrons, protons, or any ions. When bound, photons, electrons, and protons behave as though they all existed simultaneously – known as superposition principle – providing more complex interactions between matter and light than can be observed through everyday phenomena.
Quantum computers can theoretically outshone conventional computer chips at certain tasks, including genome assembling. But their practical impact remains uncertain at present. Researchers are developing algorithms that utilize existing powerful HPC systems to simulate quantum hardware; and testing these on short stretches of DNA sequence and then large genomes like COVID-19 pandemic strain.
The QLCI program allows NSF to establish and operate multidisciplinary centers for research on quantum information science, engineering and technology at the frontiers, as stipulated by both the National Quantum Initiative Act and an advisory Committee report, Sustaining American Leadership in Quantum Information Science2. The Quantum for Biology (Q4Bio) component of QLCI supports genome sequencing and assembly efforts including those which compare specific viral or bacterial genomic sequences against reference genome assemblies – this approach improves identification of species as well as can guide selection of candidate vaccines against new infectious disease threats.
