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Institution

University of Malaya

EducationKuala Lumpur, Malaysia
About: University of Malaya is a education organization based out in Kuala Lumpur, Malaysia. It is known for research contribution in the topics: Population & Fiber laser. The organization has 25087 authors who have published 51491 publications receiving 1036791 citations. The organization is also known as: UM & Universiti Malaya.


Papers
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Journal ArticleDOI
TL;DR: The objectives of this study are to highlight the effects of remote resources on the quality and reliability of augmentation processes and discuss the challenges and opportunities of employing varied cloud-based resources in augmenting mobile devices.
Abstract: Recently, Cloud-based Mobile Augmentation (CMA) approaches have gained remarkable ground from academia and industry. CMA is the state-of-the-art mobile augmentation model that employs resource-rich clouds to increase, enhance, and optimize computing capabilities of mobile devices aiming at execution of resource-intensive mobile applications. Augmented mobile devices envision to perform extensive computations and to store big data beyond their intrinsic capabilities with least footprint and vulnerability. Researchers utilize varied cloud-based computing resources (e.g., distant clouds and nearby mobile nodes) to meet various computing requirements of mobile users. However, employing cloud-based computing resources is not a straightforward panacea. Comprehending critical factors (e.g., current state of mobile client and remote resources) that impact on augmentation process and optimum selection of cloud-based resource types are some challenges that hinder CMA adaptability. This paper comprehensively surveys the mobile augmentation domain and presents taxonomy of CMA approaches. The objectives of this study is to highlight the effects of remote resources on the quality and reliability of augmentation processes and discuss the challenges and opportunities of employing varied cloud-based resources in augmenting mobile devices. We present augmentation definition, motivation, and taxonomy of augmentation types, including traditional and cloud-based. We critically analyze the state-of-the-art CMA approaches and classify them into four groups of distant fixed, proximate fixed, proximate mobile, and hybrid to present a taxonomy. Vital decision making and performance limitation factors that influence on the adoption of CMA approaches are introduced and an exemplary decision making flowchart for future CMA approaches are presented. Impacts of CMA approaches on mobile computing is discussed and open challenges are presented as the future research directions.

422 citations

Journal ArticleDOI
TL;DR: The reality of BIM, its widespread benefits and current level of uptake are discussed, as well as recommendations regarding how future BIM adoption could be developed are also highlighted.
Abstract: Rapid advancement of technology continues to leverage change and innovation in the construction industry. Continued digitization of the industry offers the opportunity to totally reinvent contemporary construction design and delivery practice for future development. Building Information Modelling (BIM) within the context of Architecture, Engineering & Construction (AEC) has been developing since the early 2000s and is considered to be a key technology. Despite major technical advancements in BIM, it has not been fully adopted and its definitive benefits have not been fully capitalized upon by industry stakeholders. The lack of widespread uptake of BIM appears to be linked to the risks and challenges that are potentially impeding its effectiveness. This paper aims to discuss the reality of BIM, its widespread benefits and current level of uptake. The risks and challenges associated with the adoption of BIM, as well as recommendations regarding how future BIM adoption could be developed are also highlighted.

417 citations

Journal ArticleDOI
Fergus J. Couch1, Xianshu Wang1, Lesley McGuffog2, Andy C. H. Lee2  +258 moreInstitutions (100)
TL;DR: It is estimated that the breast cancer lifetime risks for the5% of BRCA1 carriers at lowest risk are 28%–50% compared to 81%–100% for the 5% at highest risk, and the ovarian cancer lifetime risk is 63% or higher, based on the known cancer risk-modifying loci.
Abstract: BRCA1-associated breast and ovarian cancer risks can be modified by common genetic variants. To identify further cancer risk-modifying loci, we performed a multi-stage GWAS of 11,705 BRCA1 carriers (of whom 5,920 were diagnosed with breast and 1,839 were diagnosed with ovarian cancer), with a further replication in an additional sample of 2,646 BRCA1 carriers. We identified a novel breast cancer risk modifier locus at 1q32 for BRCA1 carriers (rs2290854, P = 2.7 x 10(-8), HR = 1.14, 95% CI: 1.09-1.20). In addition, we identified two novel ovarian cancer risk modifier loci: 17q21.31 (rs17631303, P = 1.4 x 10(-8), HR = 1.27, 95% CI: 1.17-1.38) and 4q32.3 (rs4691139, P = 3.4 x 10(-8), HR = 1.20, 95% CI: 1.17-1.38). The 4q32.3 locus was not associated with ovarian cancer risk in the general population or BRCA2 carriers, suggesting a BRCA1-specific association. The 17q21.31 locus was also associated with ovarian cancer risk in 8,211 BRCA2 carriers (P = 2 x 10(-4)). These loci may lead to an improved understanding of the etiology of breast and ovarian tumors in BRCA1 carriers. Based on the joint distribution of the known BRCA1 breast cancer risk-modifying loci, we estimated that the breast cancer lifetime risks for the 5% of BRCA1 carriers at lowest risk are 28%-50% compared to 81%-100% for the 5% at highest risk. Similarly, based on the known ovarian cancer risk-modifying loci, the 5% of BRCA1 carriers at lowest risk have an estimated lifetime risk of developing ovarian cancer of 28% or lower, whereas the 5% at highest risk will have a risk of 63% or higher. Such differences in risk may have important implications for risk prediction and clinical management for BRCA1 carriers.

417 citations

Journal ArticleDOI
10 Aug 2021-JAMA
TL;DR: In this article, a prospective meta-analysis of clinical trials of patients hospitalized for COVID-19, administration of IL-6 antagonists, compared with usual care or placebo, was associated with lower 28-day all-cause mortality.
Abstract: Importance Clinical trials assessing the efficacy of IL-6 antagonists in patients hospitalized for COVID-19 have variously reported benefit, no effect, and harm. Objective To estimate the association between administration of IL-6 antagonists compared with usual care or placebo and 28-day all-cause mortality and other outcomes. Data Sources Trials were identified through systematic searches of electronic databases between October 2020 and January 2021. Searches were not restricted by trial status or language. Additional trials were identified through contact with experts. Study Selection Eligible trials randomly assigned patients hospitalized for COVID-19 to a group in whom IL-6 antagonists were administered and to a group in whom neither IL-6 antagonists nor any other immunomodulators except corticosteroids were administered. Among 72 potentially eligible trials, 27 (37.5%) met study selection criteria. Data Extraction and Synthesis In this prospective meta-analysis, risk of bias was assessed using the Cochrane Risk of Bias Assessment Tool. Inconsistency among trial results was assessed using theI2statistic. The primary analysis was an inverse variance–weighted fixed-effects meta-analysis of odds ratios (ORs) for 28-day all-cause mortality. Main Outcomes and Measures The primary outcome measure was all-cause mortality at 28 days after randomization. There were 9 secondary outcomes including progression to invasive mechanical ventilation or death and risk of secondary infection by 28 days. Results A total of 10 930 patients (median age, 61 years [range of medians, 52-68 years]; 3560 [33%] were women) participating in 27 trials were included. By 28 days, there were 1407 deaths among 6449 patients randomized to IL-6 antagonists and 1158 deaths among 4481 patients randomized to usual care or placebo (summary OR, 0.86 [95% CI, 0.79-0.95];P = .003 based on a fixed-effects meta-analysis). This corresponds to an absolute mortality risk of 22% for IL-6 antagonists compared with an assumed mortality risk of 25% for usual care or placebo. The corresponding summary ORs were 0.83 (95% CI, 0.74-0.92;P Conclusions and Relevance In this prospective meta-analysis of clinical trials of patients hospitalized for COVID-19, administration of IL-6 antagonists, compared with usual care or placebo, was associated with lower 28-day all-cause mortality. Trial Registration PROSPERO Identifier:CRD42021230155

417 citations

Journal ArticleDOI
TL;DR: In this paper, four heavy metals such as arsenic (As), chromium (Cr), cadmium (Cd), and lead (Pb) in sediments and water were investigated from Karnaphuli River in Bangladesh.
Abstract: Contamination of heavy metals in sediment is regarded as a global crisis with a large share in developing countries like Bangladesh. Four heavy metals such as arsenic (As), chromium (Cr), cadmium (Cd) and lead (Pb) in sediments and water were investigated from Karnaphuli River in Bangladesh. The decreasing trend of metals were observed in water as Cr > As > Pb > Cd and in sediment Cr > Pb > As > Cd. The ranges of heavy metals in water were 13.31–53.87, 46.09–112.43, 2.54–18.34 and 5.29–27.45 μg/L and in sediments were 11.56–35.48, 37.23–160.32, 0.63–3.56 and 21.98–73.42 mg/kg for As, Cr, Cd and Pb. The level of studied metals in water samples exceeded the safe limits of drinking water, indicated that water from this river is not safe for drinking and/or cooking. Contamination factor (CF) confirmed that the sediment samples were moderate to high contamination by As, Cd and Pb. The pollution load index (PLI) values were above one (>1) indicates advanced decline of the sediment quality. This study recommended that continuous monitoring of As, Cd and Pb in water; sediment and other aquatic biota of Karnaphuli River should be directed to assess the risk of these vital metals to safe the ecology in the vicinity of this river.

416 citations


Authors

Showing all 25327 results

NameH-indexPapersCitations
Diederick E. Grobbee1551051122748
Intae Yu134137289870
Ovsat Abdinov12986478489
Jyothsna Rani Komaragiri129109782258
Odette Benary12884474238
Paul M. Vanhoutte12786862177
Irene Vichou12676272520
Ian O. Ellis126105175435
Louisa Degenhardt126798139683
Matthew Jones125116196909
Andrius Juodagalvis118106967138
Martin Ravallion11557055380
R. St. Denis11292165326
Xiao-Ming Chen10859642229
A. Yurkewicz10651451537
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202391
2022418
20213,698
20203,646
20193,239
20183,203