Inventory, Operations, and Safety at Free Right-Turn Ramps

SPR-FY22(012)This research focused on traffic safety and operational performance of rural, minor approach stop-controlled intersections with free right-turn (FRT) ramps. The objectives of the research were to: \u2022 Create a statewide inventory of rural FRT ramp intersections and provide to the Nebraska Department of Transportation (NDOT), \u2022 Using NDOT 10-year crash data, conduct statistical safety analysis of rural FRT intersections extending \ubc-mile in each direction from the intersection, \u2022 Study vehicular operations at rural intersections with and without FRT ramps including a comparison of vehicular conflicts, and \u2022 Develop guidelines for operations and safety tradeoffs to assist with NDOT projects on maintaining similar locations, removing, or reconstructing ramps. As of 2023, 79 FRT ramps exist at 68 rural highway intersections in Nebraska. FRT ramps may be located on three-legged or four-legged intersections and may be on the minor, the major, or both minor and major approaches of the same intersection. The research compared the 68 rural FRT ramp intersections to 24 similar non-FRT rural intersections to identify differences in crash frequencies, crash rates, and crash severity using 2010-2019 crash data from NDOT. The analysis did not show any statistically significant differences between the two intersection groups. This result is identical to a 1995 Nebraska-based study of rural FRT ramp intersection safety. The research investigated vehicular conflicts between right-turning vehicles by pairing six non-FRT intersections with six FRT ramp intersections and collecting data using video recording equipment. The comparison was between vehicular conflicts experienced by right turning traffic on the same approach of the FRT ramp and non-FRT intersections. Data analysis showed that non-FRT right-turns on the minor approach, major approach with no exclusive right-turn lane, and major approach with an exclusive right-turn lane experienced statistically significantly higher conflicts per 1,000 entering right-turning vehicles than FRT ramp intersections. A VISSIM microsimulation model of traffic operations at FRT ramp intersections and non-FRT intersections enabled the creation of 324 scenarios, based on varying traffic and roadway geometry. Assuming a 20-year lifespan, benefit cost (B/C) analysis was conducted for combinations of discount rates (4%, 6%, and 8%), major road AADT (5,000; 10,000; 15,000), minor road AADT (2,500; 5,000; 7,500), percent right turning traffic (10%, 25%, 50%), FRT ramp radius in feet (650; 1,200; 1,800) and speed limit in mph (45, 55, 65). Traffic operational benefits are the basis for considering FRT ramp construction, reconstruction, or removal at rural, minor approach stop controlled intersections in Nebraska. The reason is the absence of any discernable differences in safety at FRT ramp and comparable non- FRT intersections. NDOT can make more informed decisions on FRT ramp intersections based on guidance in this report

A New Framework for Music Education Knowledge and Skill

This study investigates perceptions of secondary school band and orchestra teachers regarding the relative importance of knowledge and skill categories to professional success, using a framework modeled after Schulman (1986, 1987). Band and orchestra teachers in secondary schools (N = 214) complete an anonymous, online survey ranking the relative importance of various knowledge and skill categories. Participants rank pedagogical content knowledge, content knowledge, and general pedagogical knowledge highest. There are no significant differences in the rankings of the categories among various subgroups at the p < .05 level. Results confirm the applicability of Schulman's model to music education. This framework has implications for undergraduate, graduate, and continuing professional education. Analysis of categories' interaction provides insight into effective classroom instruction.Yeshttps://us.sagepub.com/en-us/nam/manuscript-submission-guideline

Propaganda in an Age of Algorithmic Personalization: Expanding Literacy Research and Practice

In this commentary, the author considers the rise of algorithmic personalization and the power of propaganda as they shift the dynamic landscape of 21st‐century literacy research and practice. Algorithmic personalization uses data from the behaviors, beliefs, interests, and emotions of the target audience to provide filtered digital content, targeted advertising, and differential product pricing to online users. As persuasive genres, advertising and propaganda may demand different types of reading practices than texts whose purpose is primarily informational or argumentative. Understanding the propaganda function of algorithmic personalization may lead to a deeper consideration of texts that activate emotion and tap into audience values for aesthetic, commercial, and political purposes. Increased attention to algorithmic personalization, propaganda, and persuasion in the context of K–12 literacy education may also help people cope with sponsored content, bots, and other forms of propaganda and persuasion that now circulate online

Exome sequencing identifies genetic variants in anophthalmia and microphthalmia

Anophthalmia and microphthalmia (A/M) are rare birth defects affecting up to 2 per 10,000 live births. These conditions are manifested by the absence of an eye or reduced eye volumes within the orbit leading to vision loss. Although clinical case series suggest a strong genetic component in A/M, few systematic investigations have been conducted on potential genetic contributions owing to low population prevalence. To overcome this challenge, we utilized DNA samples and data collected as part of the National Birth Defects Prevention Study (NBDPS). The NBDPS employed multi-center ascertainment of infants affected by A/M. We performed exome sequencing on 67 family trios and identified numerous genes affected by rare deleterious nonsense and missense variants in this cohort, including de novo variants. We identified 9 nonsense changes and 86 missense variants that are absent from the reference human population (Genome Aggregation Database), and we suggest that these are high priority candidate genes for A/M. We also performed literature curation, single cell transcriptome comparisons, and molecular pathway analysis on the candidate genes and performed protein structure modeling to determine the potential pathogenic variant consequences on PAX6 in this disease

The feasibility of applying geopressured-geothermal resources to direct uses

This study concludes that direct use technologies, especially desalinated water production, can contribute significantly to the value added process and the overall economic viability in developing a geopressured resource. Although agriculture and aquaculture applications are marginal projects when they are the only use of a geopressured well, the small margin of profitability can contribute to improving the overall economics of the direct use development. The added complexity from a technical and management aspect may add to the overall risk and unpredictability of the project. Six combination of direct uses received economic evaluation that resulted in 15% discounted payback periods ranging from 4 to over 10 years. Many other combinations are possible depending on the resource and market variables. Selection of appropriate technologies and sizes of applications will be established by the developer that engages in geopressured resource utilization. Currently, many areas of the country where geopressured resources are located also have surplus electrical capacity and generation, thus power utilities have been selling power for less than 2 cents per kWH, well below a reasonable breakeven value for geopressured produced electricity. However, when the energy demand of the integrated geopressured facility is large enough to install power generation equipment, operating expenses can be reduced by not paying the 10 to 12 cents per kWH utility rate. The study includes an analysis of a geothermal turbine unit installed with a desalination and an agriculture/aquaculture facility, taking advantage of the cascading energy values. Results suggest that this scenario becomes profitable only where the market price for electricity exceeds five cents per kWH

Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data

Background: The National Birth Defects Prevention Study (NBDPS) is a multisite, population-based, case–control study of genetic and nongenetic risk factors for major structural birth defects. Eligible women had a pregnancy affected by a birth defect or a liveborn child without a birth defect between 1997 and 2011. They were invited to complete a telephone interview to collect pregnancy exposure data and were mailed buccal cell collection kits to collect specimens from themselves, their child (if living), and their child's father. Over 23,000 families representing more than 30 major structural birth defects provided DNA specimens. Methods: To evaluate their utility for exome sequencing (ES), specimens from 20 children with colonic atresia were studied. Evaluations were conducted on specimens collected using cytobrushes stored and transported in open versus closed packaging, on native genomic DNA (gDNA) versus whole genome amplified (WGA) products and on a library preparation protocol adapted to low amounts of DNA. Results: The DNA extracted from brushes in open packaging yielded higher quality sequence data than DNA from brushes in closed packaging. Quality metrics of sequenced gDNA were consistently higher than metrics from corresponding WGA products and were consistently high when using a low input protocol. Conclusions: This proof-of-principle study established conditions under which ES can be applied to NBDPS specimens. Successful sequencing of exomes from well-characterized NBDPS families indicated that this unique collection can be used to investigate the roles of genetic variation and gene–environment interaction effects in birth defect etiologies, providing a valuable resource for birth defect researchers

Personalized peptide-based vaccination for treatment of colorectal cancer: rational and progress

Colorectal cancer (CRC) is one of the most common cancers globally and is associated with a high rate of morbidity and mortality. A large proportion of patients with early stage CRC who undergo conventional treatments develop local recurrence or distant metastasis and in this group of advanced disease, the survival rate is low. Furthermore there is often a poor response and/or toxicity associated with chemotherapy and chemo-resistance may limit continuing conventional treatment alone. Choosing novel and targeted therapeutic approaches based on clinicopathological and molecular features of tumors in combination with conventional therapeutic approach could be used to eradicate residual micrometastasis and therefore improve patient prognosis and also be used preventively. Peptide-based vaccination therapy is one class of cancer treatment that could be used to induce tumor-specific immune responses, through the recognition of specific antigen-derived peptides in tumor cells, and this has emerged as a promising anti-cancer therapeutic strategy. The aim of this review was to summarize the main findings of recent studies in exciting field of peptide-based vaccination therapy in CRC patients as a novel therapeutic approach in treatment of CRC

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

The etiology of biliary atresia (BA) is unknown, but recent studies suggest a role for rare protein-altering variants (PAVs). Exome sequencing data from the National Birth Defects Prevention Study on 54 child–parent trios, one child–mother duo, and 1513 parents of children with other birth defects were analyzed. Most (91%) cases were isolated BA. We performed (1) a trio-based analysis to identify rare de novo, homozygous, and compound heterozygous PAVs and (2) a case–control analysis using a sequence kernel-based association test to identify genes enriched with rare PAVs. While we replicated previous findings on PKD1L1, our results do not suggest that recurrent de novo PAVs play important roles in BA susceptibility. In fact, our finding in NOTCH2, a disease gene associated with Alagille syndrome, highlights the difficulty in BA diagnosis. Notably, IFRD2 has been implicated in other gastrointestinal conditions and warrants additional study. Overall, our findings strengthen the hypothesis that the etiology of BA is complex

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

Bladder exstrophy (BE) is a rare, lower ventral midline defect with the bladder and part of the urethra exposed. The etiology of BE is unknown but thought to be influenced by genetic variation with more recent studies suggesting a role for rare variants. As such, we conducted paired-end exome sequencing in 26 child/mother/father trios. Three children had rare (allele frequency ≤ 0.0001 in several public databases) inherited variants in TSPAN4, one with a loss-of-function variant and two with missense variants. Two children had loss-of-function variants in TUBE1. Four children had rare missense or nonsense variants (one per child) in WNT3, CRKL, MYH9, or LZTR1, genes previously associated with BE. We detected 17 de novo missense variants in 13 children and three de novo loss-of-function variants (AKR1C2, PRRX1, PPM1D) in three children (one per child). We also detected rare compound heterozygous loss-of-function variants in PLCH2 and CLEC4M and rare inherited missense or loss-of-function variants in additional genes applying autosomal recessive (three genes) and X-linked recessive inheritance models (13 genes). Variants in two genes identified may implicate disruption in cell migration (TUBE1) and adhesion (TSPAN4) processes, mechanisms proposed for BE, and provide additional evidence for rare variants in the development of this defect