Definition of a Security: Risk Capital and Investment Contracts in Washington

The addition of the risk capital definition to Washington\u27s securities law will expand regulation to many transactions that in the past were excluded. Although its full application is unforeseeable, the risk capital definition should apply to financing arrangements in the formation of clubs, associations, and cooperatives. Practitioners must be keenly aware that ventures not traditionally defined within Washington\u27s securities regulations many now fall under the risk capital definition of a security

Solar Powered Wireless Charging Device

This MQP involves the design and implementation of a versatile charging system that integrates solar charging and wireless power transfer via inductive coupling. During this project the team designed and developed a fully-functioning product through a three-stage design plan. First, a proof of concept test bench was developed to validate our technology approach so that it functions correctly for our specific application. Second, a prototype device utilizing these concepts was developed for testing and exploration of possible improvements. Our team designed and developed this prototype based on product and performance criteria. Third, we finalized a version of our design with changes and upgrades from a suite of testing performed on our prototype

Waste Management Plan for the Technological University of Panama: Campus Victor Levi Sasso

With relatively new infrastructure, a rapidly growing population, and a desire for a more sustainable campus, the Technological University of Panama (UTP) seeks to create an advanced waste management system that accommodates all types of waste. By gathering information concerning current waste management, engaging with stakeholders, researching methods for recycling in Panama, and predicting future waste of the campus, we were able to create a comprehensive waste management plan for UTP emphasizing recycling and incorporating all classifications of waste

Consensus coding sequence (CCDS) database: a standardized set of human and mouse protein-coding regions supported by expert curation.

The Consensus Coding Sequence (CCDS) project provides a dataset of protein-coding regions that are identically annotated on the human and mouse reference genome assembly in genome annotations produced independently by NCBI and the Ensembl group at EMBL-EBI. This dataset is the product of an international collaboration that includes NCBI, Ensembl, HUGO Gene Nomenclature Committee, Mouse Genome Informatics and University of California, Santa Cruz. Identically annotated coding regions, which are generated using an automated pipeline and pass multiple quality assurance checks, are assigned a stable and tracked identifier (CCDS ID). Additionally, coordinated manual review by expert curators from the CCDS collaboration helps in maintaining the integrity and high quality of the dataset. The CCDS data are available through an interactive web page (https://www.ncbi.nlm.nih.gov/CCDS/CcdsBrowse.cgi) and an FTP site (ftp://ftp.ncbi.nlm.nih.gov/pub/CCDS/). In this paper, we outline the ongoing work, growth and stability of the CCDS dataset and provide updates on new collaboration members and new features added to the CCDS user interface. We also present expert curation scenarios, with specific examples highlighting the importance of an accurate reference genome assembly and the crucial role played by input from the research community. Nucleic Acids Res 2018 Jan 4; 46(D1):D221-D228

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

Developing ovarian cancer stem cell models: laying the pipeline from discovery to clinical intervention.

Despite decades of research, ovarian cancer is still associated with unacceptably high mortality rates, which must be addressed by novel therapeutic approaches. One avenue through which this may be achieved is targeting of tumor-initiating \u27Cancer Stem Cells\u27 (CSCs). CSCs are sufficient to generate primary and recurrent disease through extensive rounds of asymmetric division, which maintain the CSC pool while producing the tissues that form the bulk of the tumor. CSCs thrive in the harsh tumor niche, are generally refractory to therapeutic intervention and closely-linked to the Epithelial-Mesenchymal Transition process, which facilitates invasion and metastasis. While it is well-accepted that CSC-targeting must be assessed as a novel therapeutic avenue, few ovarian CSC models have been developed due to perceived and actual difficulties associated with the process of \u27CSC Discovery\u27. In this article we review contemporary approaches to CSC Discovery and argue that this process should start with an understanding of the specific challenges associated with clinical intervention, laying the pipeline backwards towards CSC Discovery. Such an approach would expedite the bridging of the gap between laboratory isolation and clinical targeting of ovarian CSCs

Catching moving targets: Cancer stem cell hierarchies, therapy-resistance & considerations for clinical intervention

It is widely believed that targeting the tumour-initiating cancer stem cell (CSC) component of malignancy has great therapeutic potential, particularly in therapy-resistant disease. However, despite concerted efforts, CSC-targeting strategies have not been efficiently translated to the clinic. This is partly due to our incomplete understanding of the mechanisms underlying CSC therapy-resistance. In particular, the relationship between therapy-resistance and the organisation of CSCs as Stem-Progenitor-Differentiated cell hierarchies has not been widely studied. In this review we argue that modern clinical strategies should appreciate that the CSC hierarchy is a dynamic target that contains sensitive and resistant components and expresses a collection of therapy-resisting mechanisms. We propose that the CSC hierarchy at primary presentation changes in response to clinical intervention, resulting in a recurrent malignancy that should be targeted differently. As such, addressing the hierarchical organisation of CSCs into our bench-side theory should expedite translation of CSC-targeting to bed-side practice. In conclusion, we discuss strategies through which we can catch these moving clinical targets to specifically compromise therapy-resistant disease

Definition of a Security: Risk Capital and Investment Contracts in Washington

The addition of the risk capital definition to Washington\u27s securities law will expand regulation to many transactions that in the past were excluded. Although its full application is unforeseeable, the risk capital definition should apply to financing arrangements in the formation of clubs, associations, and cooperatives. Practitioners must be keenly aware that ventures not traditionally defined within Washington\u27s securities regulations many now fall under the risk capital definition of a security

The significant role of sediment bio-retexturing within a contemporary carbonate platform system: Implications for carbonate microfacies development

Assessments of carbonate platform reef–lagoon sediments and benthic habitats around Rodrigues Island (south-west Indian Ocean) have been undertaken in order to examine carbonate sediment textural properties and the controls on texturally-defined sediment fabrics. Reef–lagoon sediments, sampled from across the expansive (~ 8 km wide) carbonate-dominated windward platform, principally comprise poorly sorted medium- to coarse-grained bioclastic sands, composed of a low diversity of grain constituents — predominantly non-geniculate coralline algal bioclasts. Despite a marked homogeneity in sediment compositional and grain size properties, eight distinct sediment textural groups can be identified that form a heterogeneous mosaic across the contemporary reef–lagoon system. Only along the narrow outer platform margins (reef crest, sand apron and outermost lagoon environments) do we observe consistent (predictable) transitions in sediment textural groups, where physical processes are the primary drivers of selective sediment transport and sorting. In contrast, across the main expanse of the lagoon, the sediment substrates are characterised by an irregular mosaic of texturally-defined sediment groups — formed primarily as a function of sediment bio-retexturing. The burrowing activities of alpheid and callianassid shrimps are particularly important in this respect and impart a distinctly unique textural fabric to the upper sediment horizons in the environments in which the respective organisms occur. The consequence of this is that, at the platform system scale, individual, texturally-defined sediment groups are relatively poor indicators of prevailing hydrodynamic regimes or of local sediment production, reflecting more the biological action of organisms inhabiting the substrate. This has important implications for understanding the development of carbonate sediment fabrics in the context of palaeoenvironmental reconstructions and for interpreting a key diagnostic criteria of carbonate microfacies. [Retrieved from publisher\u27s website: http://www.sciencedirect.com/science/article/pii/S0037073809001171