THEORY, DESIGN, AND SIMULATION OF LINA: A PATH FORWARD FOR QCA-TYPE NANOELECTRONICS

The past 50 years have seen exponential advances in digital integrated circuit technologies which has facilitated an explosion of uses and functionality. Although this rate (generally referred to as "Moore's Law") cannot be sustained indefinitely, significant advances will remain possible even after current technologies reach fundamental limits. However if these further advances are to be realized, nanoelectronics designs must be developed that provide significant improvements over, the currently-utilized, complementary metal-oxide semiconductor (CMOS) transistor based integrated circuits. One promising nanoelectronics paradigm to fulfill this function is Quantum-dot Cellular Automata (QCA). QCA provides the possibility of THz switching, molecular scaling, and provides particular applicability for advanced logical constructs such as reversible logic and systolic arrays within the paradigm. These attributes make QCA an exciting prospect; however, current fabrication technology does not exist which allows for the fabrication of reliable electronic QCA circuits which operate at room-temperature. Furthermore, a plausible path to fabrication of circuitry on the very large scale integration (VLSI) level with QCA does not currently exist. This has caused doubts to the viability of the paradigm and questions to its future as a suitable nanoelectronic replacement to CMOS. In order to resolve these issues, research was conducted into a new design which could utilize key attributes of QCA while also providing a means for near-term fabrication of reliable room-temperature circuits and a path forward for VLSI circuits.The result of this research, presented in this dissertation, is the Lattice-based Integrated-signal Nanocellular Automata (LINA) nanoelectronics paradigm. LINA designs are based on QCA and provide the same basic functionality as traditional QCA. LINA also retains the key attributes of THz switching, scalability to the molecular level, and ability to utilize advanced logical constructs which are crucial to the QCA proposals. However, LINA designs also provide significant improvements over traditional QCA. For example, the continuous correction of faults, due to LINA's integrated-signal approach, provides reliability improvements to enable room-temperature operation with cells which are potentially up to 20nm and fault tolerance to layout, patterning, stray-charge, and stuck-at-faults. In terms of fabrication, LINA's lattice-based structure allows precise relative placement through the use of self-assembly techniques seen in current nanoparticle research. LINA also allows for large enough wire and logic structures to enable use of widely available photo-lithographical patterning technologies. These aspects of the LINA designs, along with power, timing, and clocking results, have been verified through the use of new and/or modified simulation tools specifically developed for this purpose. To summarize, the LINA designs and results, presented in this dissertation, provide a path to realization of QCA-type VLSI nanoelectronic circuitry. Furthermore, they offer a renewed viability of the paradigm to replace CMOS and advance computing technologies beyond the next decade

Avoiding overfitting of multilayer perceptrons by training derivatives

Resistance to overfitting is observed for neural networks trained with extended backpropagation algorithm. In addition to target values, its cost function uses derivatives of those up to the $4^{\mathrm{th}}$ order. For common applications of neural networks, high order derivatives are not readily available, so simpler cases are considered: training network to approximate analytical function inside 2D and 5D domains and solving Poisson equation inside a 2D circle. For function approximation, the cost is a sum of squared differences between output and target as well as their derivatives with respect to the input. Differential equations are usually solved by putting a multilayer perceptron in place of unknown function and training its weights, so that equation holds within some margin of error. Commonly used cost is the equation's residual squared. Added terms are squared derivatives of said residual with respect to the independent variables. To investigate overfitting, the cost is minimized for points of regular grids with various spacing, and its root mean is compared with its value on much denser test set. Fully connected perceptrons with six hidden layers and $2\cdot10^{4}$, $1\cdot10^{6}$ and $5\cdot10^{6}$ weights in total are trained with Rprop until cost changes by less than 10% for last 1000 epochs, or when the $10000^{\mathrm{th}}$ epoch is reached. Training the network with $5\cdot10^{6}$ weights to represent simple 2D function using 10 points with 8 extra derivatives in each produces cost test to train ratio of $1.5$, whereas for classical backpropagation in comparable conditions this ratio is $2\cdot10^{4}$

Rapid detection of carriers with BRCA1 and BRCA2 mutations using high resolution melting analysis

<p>Abstract</p> <p>Background</p> <p>Germline inactivating mutations in <it>BRCA1 </it>and <it>BRCA2 </it>underlie a major proportion of the inherited predisposition to breast and ovarian cancer. These mutations are usually detected by DNA sequencing. Cost-effective and rapid methods to screen for these mutations would enable the extension of mutation testing to a broader population. High resolution melting (HRM) analysis is a rapid screening methodology with very low false negative rates. We therefore evaluated the use of HRM as a mutation scanning tool using, as a proof of principle, the three recurrent BRCA1 and BRCA2 founder mutations in the Ashkenazi Jewish population in addition to other mutations that occur in the same regions.</p> <p>Methods</p> <p>We designed PCR amplicons for HRM scanning of <it>BRCA1 </it>exons 2 and 20 (carrying the founder mutations185delAG and 5382insC respectively) and the part of the <it>BRCA2 </it>exon 11 carrying the 6174delT founder mutation. The analysis was performed on an HRM-enabled real time PCR machine.</p> <p>Results</p> <p>We tested DNA from the peripheral blood of 29 individuals heterozygous for known mutations. All the Ashkenazi founder mutations were readily identified. Other mutations in each region that were also readily detected included the recently identified Greek founder mutation 5331G>A in exon 20 of <it>BRCA1</it>. Each mutation had a reproducible melting profile.</p> <p>Conclusion</p> <p>HRM is a simple and rapid scanning method for known and unknown <it>BRCA1 </it>and <it>BRCA2 </it>germline mutations that can dramatically reduce the amount of sequencing required and reduce the turnaround time for mutation screening and testing. In some cases, such as tracking mutations through pedigrees, sequencing may only be necessary to confirm positive results. This methodology will allow for the economical screening of founder mutations not only in people of Ashkenazi Jewish ancestry but also in other populations with founder mutations such as Central and Eastern Europeans (<it>BRCA1 </it>5382insC) and Greek Europeans (<it>BRCA1 </it>5331G>A).</p

Predictors of linkage to care following community-based HIV counseling and testing in rural Kenya

Despite innovations in HIV counseling and testing (HCT), important gaps remain in understanding linkage to care. We followed a cohort diagnosed with HIV through a community-based HCT campaign that trained persons living with HIV/AIDS (PLHA) as navigators. Individual, interpersonal, and institutional predictors of linkage were assessed using survival analysis of self-reported time to enrollment. Of 483 persons consenting to follow-up, 305 (63.2%) enrolled in HIV care within 3 months. Proportions linking to care were similar across sexes, barring a sub-sample of men aged 18–25 years who were highly unlikely to enroll. Men were more likely to enroll if they had disclosed to their spouse, and women if they had disclosed to family. Women who anticipated violence or relationship breakup were less likely to link to care. Enrolment rates were significantly higher among participants receiving a PLHA visit, suggesting that a navigator approach may improve linkage from community-based HCT campaigns.Vestergaard Frandse

A sensitive one-step real-time PCR for detection of avian influenza viruses using a MGB probe and an internal positive control

BACKGROUND: Avian influenza viruses (AIVs) are endemic in wild birds and their introduction and conversion to highly pathogenic avian influenza virus in domestic poultry is a cause of serious economic losses as well as a risk for potential transmission to humans. The ability to rapidly recognise AIVs in biological specimens is critical for limiting further spread of the disease in poultry. The advent of molecular methods such as real time polymerase chain reaction has allowed improvement of detection methods currently used in laboratories, although not all of these methods include an Internal Positive Control (IPC) to monitor for false negative results. Therefore we developed a one-step reverse transcription real time PCR (RRT-PCR) with a Minor Groove Binder (MGB) probe for the detection of different subtypes of AIVs. This technique also includes an IPC. METHODS: RRT-PCR was developed using an improved TaqMan technology with a MGB probe to detect AI from reference viruses. Primers and probe were designed based on the matrix gene sequences from most animal and human A influenza virus subtypes. The specificity of RRT-PCR was assessed by detecting influenza A virus isolates belonging to subtypes from H1–H13 isolated in avian, human, swine and equine hosts. The analytical sensitivity of the RRT-PCR assay was determined using serial dilutions of in vitro transcribed matrix gene RNA. The use of a rodent RNA as an IPC in order not to reduce the efficiency of the assay was adopted. RESULTS: The RRT-PCR assay is capable to detect all tested influenza A viruses. The detection limit of the assay was shown to be between 5 and 50 RNA copies per reaction and the standard curve demonstrated a linear range from 5 to 5 × 10(8 )copies as well as excellent reproducibility. The analytical sensitivity of the assay is 10–100 times higher than conventional RT-PCR. CONCLUSION: The high sensitivity, rapidity, reproducibility and specificity of the AIV RRT-PCR with the use of IPC to monitor for false negative results can make this method suitable for diagnosis and for the evaluation of viral load in field specimens

The Formation of the First Massive Black Holes

Supermassive black holes (SMBHs) are common in local galactic nuclei, and SMBHs as massive as several billion solar masses already exist at redshift z=6. These earliest SMBHs may grow by the combination of radiation-pressure-limited accretion and mergers of stellar-mass seed BHs, left behind by the first generation of metal-free stars, or may be formed by more rapid direct collapse of gas in rare special environments where dense gas can accumulate without first fragmenting into stars. This chapter offers a review of these two competing scenarios, as well as some more exotic alternative ideas. It also briefly discusses how the different models may be distinguished in the future by observations with JWST, (e)LISA and other instruments.Comment: 47 pages with 306 references; this review is a chapter in "The First Galaxies - Theoretical Predictions and Observational Clues", Springer Astrophysics and Space Science Library, Eds. T. Wiklind, V. Bromm & B. Mobasher, in pres