Wavelet Decomposition for the Detection and Diagnosis of Faults in Rolling Element Bearings

Condition monitoring and fault diagnosis of equipment and processes are of great concern in industries. Early fault detection in machineries can save millions of dollars in emergency maintenance costs. This paper presents a wavelet-based analysis technique for the diagnosis of faults in rotating machinery from its mechanical vibrations. The choice between the discrete wavelet transform and the discrete wavelet packet transform is discussed, along with the choice of the mother wavelet and some of the common extracted features. It was found that the peak locations in spectrum of the vibration signal could also be efficiently used in the detection of a fault in ball bearings. For the identification of fault location and its size, best results were obtained with the root mean square extracted from the terminal nodes of a wavelet tree of Symlet basis fed to Bayesian classier

A Distinctive Pattern of Diversity for the TAS2R38 Gene in North Africa

The TAS2R38 gene is involved in bitter taste perception. This study documents the distinctive diversity patterns in Northern Africa of functional SNPs rs713598 and rs1726866 at the TAS2R38 locus and places those patterns in the context of global TAS2R38 diversity. We analyzed data previously genotyped with Taqman Applied Biosystem for rs713598 and rs1726866 for 375 unrelated subjects (305 Tunisians from seven locations: Mahdia, Sousse, Kesra, Nebeur, Kairouan, Smar and Kerkennah plus 70 Libyans). Data were analyzed to present haplotypes and genotypes and were compared to the data from worldwide populations. We provide information about TAS2R38 diversity in a part of the world that is relatively under-studied. Considering respectively the two SNPs rs713598 and rs1726866, the (C-A) nucleotide haplotype leading to PV amino acid haplotype is extremely rare almost everywhere, but it is relatively frequent (between 6% and 10%) in Northern Africa where it does coexist with the globally common haplotypes (PA, AA and AV). Given its higher frequency in Northern Africa, we propose the (C-A) haplotype as a biogeographic marker for forensic purposes

Comparison between Scheduling Techniques in Long Term Evolution

Long-Term Evolution (LTE) is a recently evolving technology characterized by very high speed data rate that allows users to access internet through their mobile as well as through other electronic devices.  Such technology is intended to support variety of IP-based heterogeneous traffic types. Traffic scheduling plays an important role in LTE technology by assigning the shared resources among users in the most efficient manner. This paper discusses the performance of three types of scheduling algorithms namely: Round Robin, best Channel Quality Indicator (CQI) and Proportional Fair (PF) schedulers representing the extreme cases in scheduling. The scheduling algorithms performances on the downlink were measured in terms of throughput and block error rate using a MATLAB-based system level simulation. Results indicate that the best CQI algorithm outperforms other algorithms in terms of throughput levels but on the expense of fairness to other users suffering from bad channel conditions. ABSTRAK: Teknologi baru Evolusi Jangka Panjang (LTE) sentiasa berubah dan ia bercirikan kelajuan kadar data sangat tinggi yang membolehkan pengguna mengakses internet melalui telefon bimbit dan peranti elektronik lain. Teknologi seperti ini bertujuan menyokong pelbagai jenis trafik heterogen berasaskan IP. Penjadualan trafik memainkan peranan penting dalam teknologi LTE bagi mengagihkan sumber perkongsian secara paling berkesan di kalangan pengguna. Kertas ini membincangkan prestasi tiga jenis algoritma penjadualan iaitu: pusingan Robin, penunjuk kualiti saluran (CQI) terbaik dan  penjadualan berkadar adil (PF) yang merupakan kes ekstrem dalam penjadualan. Prestasi penjadualan Algoritma di pautan turun diukur dari segi daya pemprosesan dan kadar ralat blok melalui simulasi  sistem menggunakan MATLAB. Hasil kajian menunjukkan algoritma CQI adalah yang terbaik berbanding hasil algoritma lain dari segi tahap daya pemprosesan tetapi algoritma ini menyebabkan pengguna lain mengalami keadaan saluran buruk. KEYWORDS: LTE; round robin; best CQI; proportional fair; scheduling; resource block

Performance evaluation of unified medical language system®'s synonyms expansion to query PubMed

<p>Abstract</p> <p>Background</p> <p>PubMed is the main access to medical literature on the Internet. In order to enhance the performance of its information retrieval tools, primarily non-indexed citations, the authors propose a method: expanding users' queries using Unified Medical Language System' (UMLS) synonyms i.e. all the terms gathered under one unique Concept Unique Identifier.</p> <p>Methods</p> <p>This method was evaluated using queries constructed to emphasize the differences between this new method and the current PubMed automatic term mapping. Four experts assessed citation relevance.</p> <p>Results</p> <p>Using UMLS, we were able to retrieve new citations in 45.5% of queries, which implies a small increase in recall. The new strategy led to a heterogeneous 23.7% mean increase in non-indexed citation retrieved. Of these, 82% have been published less than 4 months earlier. The overall mean precision was 48.4% but differed according to the evaluators, ranging from 36.7% to 88.1% (Inter rater agreement was poor: kappa = 0.34).</p> <p>Conclusions</p> <p>This study highlights the need for specific search tools for each type of user and use-cases. The proposed strategy may be useful to retrieve recent scientific advancement.</p

Tumor markers in breast cancer - European Group on Tumor Markers recommendations

Recommendations are presented for the routine clinical use of serum and tissue-based markers in the diagnosis and management of patients with breast cancer. Their low sensitivity and specificity preclude the use of serum markers such as the MUC-1 mucin glycoproteins ( CA 15.3, BR 27.29) and carcinoembryonic antigen in the diagnosis of early breast cancer. However, serial measurement of these markers can result in the early detection of recurrent disease as well as indicate the efficacy of therapy. Of the tissue-based markers, measurement of estrogen and progesterone receptors is mandatory in the selection of patients for treatment with hormone therapy, while HER-2 is essential in selecting patients with advanced breast cancer for treatment with Herceptin ( trastuzumab). Urokinase plasminogen activator and plasminogen activator inhibitor 1 are recently validated prognostic markers for lymph node-negative breast cancer patients and thus may be of value in selecting node-negative patients that do not require adjuvant chemotherapy. Copyright (C) 2005 S. Karger AG, Basel

Integrated Genomic and Gene Expression Profiling Identifies Two Major Genomic Circuits in Urothelial Carcinoma

Similar to other malignancies, urothelial carcinoma (UC) is characterized by specific recurrent chromosomal aberrations and gene mutations. However, the interconnection between specific genomic alterations, and how patterns of chromosomal alterations adhere to different molecular subgroups of UC, is less clear. We applied tiling resolution array CGH to 146 cases of UC and identified a number of regions harboring recurrent focal genomic amplifications and deletions. Several potential oncogenes were included in the amplified regions, including known oncogenes like E2F3, CCND1, and CCNE1, as well as new candidate genes, such as SETDB1 (1q21), and BCL2L1 (20q11). We next combined genome profiling with global gene expression, gene mutation, and protein expression data and identified two major genomic circuits operating in urothelial carcinoma. The first circuit was characterized by FGFR3 alterations, overexpression of CCND1, and 9q and CDKN2A deletions. The second circuit was defined by E3F3 amplifications and RB1 deletions, as well as gains of 5p, deletions at PTEN and 2q36, 16q, 20q, and elevated CDKN2A levels. TP53/MDM2 alterations were common for advanced tumors within the two circuits. Our data also suggest a possible RAS/RAF circuit. The tumors with worst prognosis showed a gene expression profile that indicated a keratinized phenotype. Taken together, our integrative approach revealed at least two separate networks of genomic alterations linked to the molecular diversity seen in UC, and that these circuits may reflect distinct pathways of tumor development

The effect of tobacco, XPC, ERCC2 and ERCC5 genetic variants in bladder cancer development

<p>Abstract</p> <p>Background</p> <p>In this work, we have conducted a case-control study in order to assess the effect of tobacco and three genetic polymorphisms in <it>XPC, ERCC2 and ERCC5 </it>genes (rs2228001, rs13181 and rs17655) in bladder cancer development in Tunisia. We have also tried to evaluate whether these variants affect the bladder tumor stage and grade.</p> <p>Methods</p> <p>The patients group was constituted of 193 newly diagnosed cases of bladder tumors. The controls group was constituted of non-related healthy subjects. The rs2228001, rs13181 and rs17655 polymorphisms were genotyped using a polymerase chain reaction-restriction fragment length polymorphism technique.</p> <p>Results</p> <p>Our data have reported that non smoker and light smoker patients (1-19PY) are protected against bladder cancer development. Moreover, light smokers have less risk for developing advanced tumors stage. When we investigated the effect of genetic polymorphisms in bladder cancer development we have found that ERCC2 and ERCC5 variants were not implicated in the bladder cancer occurrence. However, the mutated homozygous genotype for XPC gene was associated with 2.09-fold increased risk of developing bladder cancer compared to the control carrying the wild genotype (p = 0.03, OR = 2.09, CI 95% 1.09-3.99). Finally, we have found that the XPC, ERCC2 and ERCC5 variants don't affect the tumors stage and grade.</p> <p>Conclusion</p> <p>These results suggest that the mutated homozygous genotype for XPC gene was associated with increased risk of developing bladder. However we have found no association between rs2228001, rs13181 and rs17655 polymorphisms and tumors stage and grade.</p