37 research outputs found
The emergent structures in digital engineering work:what can we learn from dynamic DSMs of near-identical systems design projects?
Design structure matrices (DSMs) are widely known for their ability to support engineers in the management of dependencies across product and organisational architectures. Recent work in the field has exploited product lifecycle management systems to generate DSMs via the co-occurrence of edits to engineering files. These are referred to as dynamic DSMs and results have demonstrated both the efficacy and accuracy of dynamic DSMs in representing engineering work and emergent product architectures. The wide-ranging applicability of the theoretical model and associated analytical process to generate dynamic DSMs enables investigations into the evolving structures within digital engineering work. This paper uses this new capability and presents the results of the world's first comparison of dynamic DSMs from a set of near-identical systems design projects. Through comparison of the dynamic DSMs' end-of-project state, change propagation characteristics and evolutionary behaviour, 10 emergent structures are elicited. These emergent structures are considered in the context of team performance and design intent in order to explain and code the identified structures. The significance of these structures for the management of future systems design projects in terms of productivity and efficacy is also described.</p
Meeting the requirements for supporting engineering design communication – Partbook
The Engineering Design Environment is evolving in many ways. Considerable amounts of data, information and knowledge are 'building up' within engineering companies and engineers are becoming involved in ever-more distributed collaboration activities to tackle complex multi-disciplinary challenges in the design of new products requiring the need to share knowledge. These changes are placing further challenges on Engineering Design Communication (EDC, a fundamental knowledge sharing activity) as the current methods of communication were never specifically designed to support such technical and highly-contextual communication. Much research has been performed on understanding EDC, thus enabling a list of requirements to support EDC to be generated. Therefore, this paper proposes a prescriptive tool, (PartBook) which instantiates these requirements and looks at the next steps being taken to evaluate the tool in meeting the requirements
Supporting engineering design communication using a custom-built social media tool - PartBook
The Issues & Challenges of 3D Managed Print Services: Towards a Support Tool for 3D Managed Print Services
Extrusion 3D printing has seen a rapid growth across many engineering sectors and is expected to triple in market value over the next decade. This is partly due to a step change in capability and increase in demand for the technology, and is leading to a requirement for 3D Managed Print Services (3D MPSs). This is where queues of prints are being received from multiple users and sent to multiple 3D printers. Examples of this include, Universities, where printers are being increasingly used in teaching, and the growing industry commonly referred to as Fabrication Laboratories (FabLabs). Given the above situation, this paper argues that gaps exist in the capability of current software and support tools to offer appropriate support for 3D MPSs. To begin to address this, this paper discusses the key issues and challenges introduced by 3D MPSs, which continues into a proposition for a support tool for 3DMPSs. The paper then demonstrates the current development of this tool with the current focus of maximising 3D printer productivity. Through the application of this tool, it is proposed that a substantial gain in productivity can be achieved
Understanding the Engineering Design Process through the Evolution of Engineering Digital Objects
Supporting engineering design communication through a social media tool - Insights for engineering project management
Investigating the effect of scale and scheduling strategies on the productivity of 3D managed print services
Sales of extrusion 3D printers have seen a rapid growth and the market value is expected to triple over the next decade. This rapid growth can be attributed to a step change in capability and an increase in demand for 3D printed parts within mechanical, industrial and civil engineering processes. Correspondingly, a new technical prototyping platform – commonly referred to as Fabrication Laboratories – has emerged to provide a stimulus for local education, entrepreneurship, innovation and invention through the provision of on-demand 3D printing and prototyping services. Central to the effectiveness of the on-demand 3D printing and prototyping services – hereby referred to as 3D managed print services – is their ability to handle multiple users with varying knowledge and understanding of the manufacturing processes and scaling numbers of 3D printers in order to maximise productivity of the service. It is this challenge of productivity and more specifically the scalability and scheduling of prints that is considered in this article. The effect of scale and scheduling strategies on productivity is investigated through the modelling of four scheduling strategies for 3D managed print service of varying scales by altering the number of available printers and level of user demand. The two most common approaches (first-come first-serve and on-line continuous queue) and two alternatives based on bed space optimisation (first-fit decreasing height and first-fit decreasing height with a genetic algorithm) have been considered. Through Monte-Carlo simulation and comparison of the strategies, it is shown that increasing the scale of 3D managed print service improves the peak productivity and range of user demands at which the 3D managed print service remain productive. In addition, the alternative strategies are able to double the peak productivity of 3D managed print service as well as increase the user demand range where the 3D managed print service remains productive. </jats:p
A rank-3 network representation for single-affiliation systems
Single-affiliation systems are observed across nature and society. Examples
include collaboration, organisational affiliations, and trade-blocs. The study
of such systems is commonly approached through network analysis. Multilayer
networks extend the representation of network analysis to include more
information through increased dimensionality. Thus, they are able to more
accurately represent the systems they are modelling. However, multilayer
networks are often represented by rank-4 adjacency tensors, resulting in a N2M2
solution space. Single-affiliation systems are unable to occupy the full extent
of this space leading to sparse data where it is difficult to attain
statistical confidence through subsequent analysis. To overcome these
limitations, this paper presents a rank-3 tensor representation for
single-affiliation systems. The representations is able to maintain full
information of single-affiliation networks in directionless networks, maintain
near full information in directed networks, reduce the solution space it
resides in (N2M) leading to statistically significant findings, and maintain
the analytical capability of multilayer approaches. This is shown through a
comparison of the rank-3 and rank-4 representations which is performed on two
datasets: the University of Bath departmental journal co-authorship 2000-2017
and an Erdos-Renyi network with random single-affiliation. The results
demonstrate that the structure of the network is maintained through both
representations, while the rank-3 representation provides greater statistical
confidence in node-based measures, and can readily show inter- and
intra-affiliation dynamics.Comment: 17 pages, 11 figure
A 3D in vitro model of the human breast duct:A method to unravel myoepithelial-luminal interactions in the progression of breast cancer
Abstract Background 3D modelling fulfils a critical role in research, allowing for complex cell behaviour and interactions to be studied in physiomimetic conditions. With tissue banks becoming established for a number of cancers, researchers now have access to primary patient cells, providing the perfect building blocks to recreate and interrogate intricate cellular systems in the laboratory. The ducts of the human breast are composed of an inner layer of luminal cells supported by an outer layer of myoepithelial cells. In early-stage ductal carcinoma in situ, cancerous luminal cells are confined to the ductal space by an intact myoepithelial layer. Understanding the relationship between myoepithelial and luminal cells in the development of cancer is critical for the development of new therapies and prognostic markers. This requires the generation of new models that allows for the manipulation of these two cell types in a physiological setting. Methods Using access to the Breast Cancer Now Tissue Bank, we isolated pure populations of myoepithelial and luminal cells from human reduction mammoplasty specimens and placed them into 2D culture. These cells were infected with lentiviral particles encoding either fluorescent proteins, to facilitate cell tracking, or an inducible human epidermal growth factor receptor 2 (HER2) expression construct. Myoepithelial and luminal cells were then recombined in collagen gels, and the resulting cellular structures were analysed by confocal microscopy. Results Myoepithelial and luminal cells isolated from reduction mammoplasty specimens can be grown separately in 2D culture and retain their differentiated state. When recombined in collagen gels, these cells reform into physiologically reflective bilayer structures. Inducible expression of HER2 in the luminal compartment, once the bilayer has formed, leads to robust luminal filling, recapitulating ductal carcinoma in situ, and can be blocked with anti-HER2 therapies. Conclusions This model allows for the interaction between myoepithelial and luminal cells to be investigated in an in-vitro environment and paves the way to study early events in breast cancer development with the potential to act as a powerful drug discovery platform