Energy saving and reliability for Wireless Body Sensor Networks (WBSN)

In healthcare and medical applications, the energy consumption of biosensor nodes affects the collection of biomedical data packets, which are sensed and measured from the human body and then transmitted toward the sink node. Nodes that are near to the sink node consume more energy as all biomedical packets are aggregated through these nodes when communicated to sink node. Each biosensor node in a wireless body sensor networks (WBSNs) such as ECG (Electrocardiogram), should provide accurate biomedical data due to the paramount importance of patient information. We propose a technique to minimise energy consumed by biosensor nodes in the bottleneck zone for WBSNs, which applies the Coordinated Duty Cycle Algorithm (CDCA) to all nodes in the bottleneck zone. Superframe order (SO) selection in CDCA is based on real traffic and the priority of the nodes in the WBSN. Furthermore, we use a special case of network coding, called Random Linear Network coding (RLNC), to encode the biomedical packets to improve reliability through calculating the probability of successful reception (PSR) at the sink node. It can be concluded that CDCA outperforms other algorithms in terms of energy saving as it achieves energy savings for most biosensor nodes in WBSNs. RLNC employs relay nodes to achieve the required level of reliability in WBSNs and to guarantee that the biomedical data is delivered correctly to the sink nod

Proceedings of the CSE 2017 Annual PGR Symposium (CSE-PGSym17)

Welcome to the Proceedings of the second Annual Postgraduate Research Symposium of the School of Computing, Science and Engineering (CSE-PGSym 2017). After the success of the first symposium, the school is delighted to run its second symposium which is being held in The Old Fire Station on 17th March 2017. The symposium is organised by the Salford Innovation Research Centre (SIRC) to provide a forum for the PGR community in the school to share their research work, engage with their peers and staff and stimulate new ideas. In line with SIRC’s strategy, the symposium aims to bring together researchers from the six groups that make up the centre to engage in multidisciplinary discussions and collaborations. It also aims to contribute to the creation of a collaborative environment within the Research Centre and the Groups and share information and explore new ideas. This is also aligned with the University’s ICZ (Industrial Collaboration Zone) programme for creating cultural, physical and virtual environments for collaboration, innovation and learning

SPARC 2018 Internationalisation and collaboration : Salford postgraduate annual research conference book of abstracts

Welcome to the Book of Abstracts for the 2018 SPARC conference. This year we not only celebrate the work of our PGRs but also the launch of our Doctoral School, which makes this year’s conference extra special. Once again we have received a tremendous contribution from our postgraduate research community; with over 100 presenters, the conference truly showcases a vibrant PGR community at Salford. These abstracts provide a taster of the research strengths of their works, and provide delegates with a reference point for networking and initiating critical debate. With such wide-ranging topics being showcased, we encourage you to take up this great opportunity to engage with researchers working in different subject areas from your own. To meet global challenges, high impact research inevitably requires interdisciplinary collaboration. This is recognised by all major research funders. Therefore engaging with the work of others and forging collaborations across subject areas is an essential skill for the next generation of researchers

Leptin improves the in vitro development of preimplantation rabbit embryos under oxidative stress of cryopreservation.

Vitrification is an economically effective method for embryo cryopreservation in human and livestock animals; however, it carries the risk of damage by the exposure to severe oxidative stress. The present study was conducted to evaluate the effect of leptin at different levels on the in vitro development of fresh and vitrified preimplantation embryos in a rabbit model. Normal embryos at morulae stage were randomly cultured for 2 h with 0, 10, 20 or 100 ng/mL of leptin, then were cultured for further 48 h as freshly or after vitrification. Thereafter, developed blastocysts form the best leptin level in fresh and vitrified embryos along with their controls were allocated to analyze the pro-oxidant (malondialdehyde, MDA; nitric oxide, NO), antioxidant (total antioxidant capacity, TAC; superoxide dismutase, SOD; glutathione peroxidase, GPx), apoptotic (Bcl-2 associated X protein, BAX; heat shock 60kD protein member 1, HSP60; tumor necrosis factor alpha, TNFα) and developmental (sex determining region Y box protein 2, SOX2; Nanog homeobox protein, NANOG; Octamer-binding protein 4, OCT4) biomarkers. Results indicate that expanding and hatching rates of embryos were significantly higher at 20 ng/mL leptin than the other levels, while vitrification had an independent suppression effect on the in vitro development rates. The MDA and NO were significantly higher, while TAC, SOD and GPx were significantly lower in the vitrified than fresh embryos. In contrast, leptin treatment significantly decreased the pro-oxidant biomarkers and increased the antioxidant biomarkers in both fresh and vitrified embryos. Vitrification significantly increased the antiapoptotic biomarkers, and decreased the developmental biomarkers in embryos. In contrast, leptin decreased the BAX and TNFα, increased the HSP60, and moreover, ameliorated the reduction of developmental biomarkers in the vitrified embryos. These results conclude that leptin could be used as antiapoptotic and antioxidant promotor to support the in vitro embryonic development, particularly under oxidative stress emerged from cryopreservation programs