9 research outputs found

    Free Vibrations of Multilayered Orthotropic Ribbed Cylindrical Shells With Attached Solid Bodies

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    Kairov, A. S. Free Vibrations of Multilayered Orthotropic Ribbed Cylindrical Shells With Attached Solid Bodies / A. S. Kairov, O. I. Vlasov // Intern. Journ. of mechanical engineering and information technology. – 2018. – Vol. 06, iss. 03. – P. 1772–1777.It is considered the problem of investigation of free vibrations of elastic multilayer orthotropic cylindrical shells made of a composite material with reinforcing ribs and attached solid bodies. A more precise mathematical model of vibrations is developed in the linear equation, which takes into consideration the structural heterogeneity of the shell system. The solution is obtained by the Ritz variational method. The results of a numerical investigation of natural frequencies and free vibration forms of supported cylindrical shells are presented

    Calculation of characteristics of hydrodynamical bearing with defined profile of sleeves based on Mathcad

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    Стаття присвячена проблемам моделювання роботи гідродинамічних опор ковзання в умовах рідинного тертя. Метою роботи є створення автоматизованої системи розрахунку характеристик опор ковзання з втулками довільного (гладкого) профілю. З цією метою розроблені методика і алгоритм вирішення задачі визначення несучої здатності опори ковзання з заданим профілем втулки, а також розроблені рекомендації з отримання раціональних профілів втулок підшипників ковзання. На базі даної методики розроблено систему розрахунку характеристик підшипника ковзання з застосуванням пакета комп'ютерної алгебри Mathcad. Розроблена розрахункова система була використана для пошуку варіантів раціонального профілювання втулки опори ковзання. Були знайдені варіанти профілю втулок опор ковзання, що забезпечують збільшення несучої здатності в порівнянні з опорами, в яких застосовується традиційний (круглий) профіль втулки. Також розроблена система дозволяє проводити експрес-порівняння характеристик опор ковзання з різними профілями втулки.The article is devoted to problems of hydrodynamic simulations of sliding friction in the liquid. The aim is to create an automated system for calculating the characteristics of sliding sleeves with arbitrary (smooth) profile. For this purpose developed a technique and algorithm for determining the carrying capacity of the bearing with arbitrary profile of the sliding sleeve, and developed recommendations for obtaining rational profiles of sleeve of bearing. On the basis of this methodology developed a system for calculating the characteristics of sliding bearing with the use of package of computer algebra Mathcad. Developed calculation system was used to search for variants of rational profiling of sleeve of sliding bearings. Were found variants of profile of sliding sleeves that provide an increase in carrying capacity compared with the supports that use traditional (round) profile of the sleeve. Designed system also allows quick comparison of the characteristics of sliding sleeves with different profiles.Статья посвящена проблемам моделирования работы гидродинамических опор скольжения в условиях жидкостного трения. Целью работы является создание автоматизированной системы расчета характеристик опор скольжения с втулками произвольного (гладкого) профиля. С этой целью разработаны методика и алгоритм решения задачи определения несущей способности опоры скольжения с задаваемым профилем втулки, а также разработаны рекомендации по получению рациональных профилей втулок подшипников скольжения. На базе данной методики разработана система расчета характеристик подшипника скольжения с применением пакета компьютерной алгебры Mathcad. Разработанная расчетная система была использована для поиска вариантов рационального профилирования втулки опоры скольжения. Были найдены варианты профиля втулок опор скольжения, обеспечивающие увеличение несущей способности по сравнению с опорами, в которых применяется традиционный (круглый) профиль втулки. Также разработанная система позволяет проводить экспресс-сравнение характеристик опор скольжения с различными профилями втулки

    Собственные колебания конструктивно неоднородных многослойных ортотропных цилиндрических оболочек из композиционных материалов

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    Каиров, А. С. Собственные колебания конструктивно неоднородных многослойных ортотропных цилиндрических оболочек из композиционных материалов = Free vibrations of constructional non-homogeneous multilayer orthotropic composite cylindrical shells / А. С. Каиров, О. И. Власов, Л. А. Латанская // Фізико-матератичні науки : вісн. ЗНУ. – Запоріжжя : ЗНУ, 2017. – № 2. – С. 57–65.Досліджено вільні коливання пружних багатошарових ортотропних циліндричних оболонок обертання з приєднаними твердими тілами. Розроблена уточнена математична модель коливань, що враховує структурну неоднорідність оболонки. Задача розв’язується в лінійній постановці методом Рітца. Наведено результати розрахунку власних частот і форм вільних коливань оболонкової системи. Виконано порівняння отриманих даних з чисельними результатами для аналогічних задач.Multilayer composite shells constructions are widespread in modern technic. That is why the problems which deal with the constructional non-homogeneous shells oscillation is rather actual. The presence of attached solid bodies, constructional features and composite orthotropic material creates a local inertial inhomogeneity and essential influence on the shells dynamic characteristics. The main aim of this work is to investigate the composite orthotropic material, the direction of reinforcing fibers layers and the attached solid bodies influence on the thin rotation shells oscillation forms and frequencies. The influence of reinforcing fibers orientation on the shells oscillations amplitudes and frequencies has been investigated by means of the new developed calculation method. The solution of this problem has been based on the Ritz method and developed mathematical model usage. The shells stress-strained state has been considered on the base Kirghof-Lyav’s linear hypothesis. According to the OstrogradskyHamiltons principle the problems solution is reduced to the variational equality. In this equality the Lagrange’s functional for the non-homogeneuos shells system consists of the sum of the shell functional and attached solid bodies functions addition. The main problem of the research is simplified by the Kholetsky matrix method usage. Thus the shells system oscillation natural frequencies and forms are calculated by the combination of Kholetsky and Hausholder’s matrix method usage for QR reverse iterations. The obtained frequencies have also been compared with the results of calculation, based on ANSYS program and show good convergence. The numerical results achieved on the base of the developed mathematical model show that the location of orthotropic layers and attached solid bodies sharply influence the thin shells oscillation forms and frequencies. The new dependences and mechanical effects, caused by the shells constructional nonhomogeneity are rather important and should be used in practice.Исследованы свободные колебания упругих многослойных ортотропных цилиндрических оболочек вращения с присоединенными твердыми телами. Разработана уточненная математическая модель колебаний, учитывающая конструктивную неоднородность оболочки. Задача решается в линейной постановке методом Ритца. Приведены результаты расчета собственных частот и форм свободных колебаний оболочечной системы. Выполнено сопоставление полученных данных с численными результатами для аналогичных задач

    Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016

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    : O1 The metabolomics approach to autism: identification of biomarkers for early detection of autism spectrum disorder A. K. Srivastava, Y. Wang, R. Huang, C. Skinner, T. Thompson, L. Pollard, T. Wood, F. Luo, R. Stevenson O2 Phenome-wide association study for smoking- and drinking-associated genes in 26,394 American women with African, Asian, European, and Hispanic descents R. Polimanti, J. Gelernter O3 Effects of prenatal environment, genotype and DNA methylation on birth weight and subsequent postnatal outcomes: findings from GUSTO, an Asian birth cohort X. Lin, I. Y. Lim, Y. Wu, A. L. Teh, L. Chen, I. M. Aris, S. E. Soh, M. T. Tint, J. L. MacIsaac, F. Yap, K. Kwek, S. M. Saw, M. S. Kobor, M. J. Meaney, K. M. Godfrey, Y. S. Chong, J. D. Holbrook, Y. S. Lee, P. D. Gluckman, N. Karnani, GUSTO study group O4 High-throughput identification of specific qt interval modulating enhancers at the SCN5A locus A. Kapoor, D. Lee, A. 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Fogelman O19 DDIT4 gene expression as a prognostic marker in several malignant tumors L. Bravo, W. Fajardo, H. Gomez, C. Castaneda, C. Rolfo, J. A. Pinto O20 Spatial organization of the genome and genomic alterations in human cancers K. C. Akdemir, L. Chin, A. Futreal, ICGC PCAWG Structural Alterations Group O21 Landscape of targeted therapies in solid tumors S. Patterson, C. Statz, S. Mockus O22 Genomic analysis reveals novel drivers and progression pathways in skin basal cell carcinoma S. N. Nikolaev, X. I. Bonilla, L. Parmentier, B. King, F. Bezrukov, G. Kaya, V. Zoete, V. Seplyarskiy, H. Sharpe, T. McKee, A. Letourneau, P. Ribaux, K. Popadin, N. Basset-Seguin, R. Ben Chaabene, F. Santoni, M. Andrianova, M. Guipponi, M. Garieri, C. Verdan, K. Grosdemange, O. Sumara, M. Eilers, I. Aifantis, O. Michielin, F. de Sauvage, S. Antonarakis O23 Identification of differential biomarkers of hepatocellular carcinoma and cholangiocarcinoma via transcriptome microarray meta-analysis S. Likhitrattanapisal O24 Clinical validity and actionability of multigene tests for hereditary cancers in a large multi-center study S. Lincoln, A. Kurian, A. Desmond, S. Yang, Y. Kobayashi, J. Ford, L. Ellisen O25 Correlation with tumor ploidy status is essential for correct determination of genome-wide copy number changes by SNP array T. L. Peters, K. R. Alvarez, E. F. Hollingsworth, D. H. Lopez-Terrada O26 Nanochannel based next-generation mapping for interrogation of clinically relevant structural variation A. Hastie, Z. Dzakula, A. W. Pang, E. T. Lam, T. Anantharaman, M. Saghbini, H. Cao, BioNano Genomics O27 Mutation spectrum in a pulmonary arterial hypertension (PAH) cohort and identification of associated truncating mutations in TBX4 C. Gonzaga-Jauregui, L. Ma, A. King, E. Berman Rosenzweig, U. Krishnan, J. G. Reid, J. D. Overton, F. Dewey, W. K. Chung O28 NORTH CAROLINA macular dystrophy (MCDR1): mutations found affecting PRDM13 K. Small, A. DeLuca, F. Cremers, R. A. Lewis, V. 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Knoppers, Global Alliance for Genomics and Health - Regulatory and Ethics Working Group O33 High throughput screening platform of competent sineups: that can enhance translation activities of therapeutic target H. Takahashi, K. R. Nitta, A. Kozhuharova, A. M. Suzuki, H. Sharma, D. Cotella, C. Santoro, S. Zucchelli, S. Gustincich, P. Carninci O34 The undiagnosed diseases network international (UDNI): clinical and laboratory research to meet patient needs J. J. Mulvihill, G. Baynam, W. Gahl, S. C. Groft, K. Kosaki, P. Lasko, B. Melegh, D. Taruscio O36 Performance of computational algorithms in pathogenicity predictions for activating variants in oncogenes versus loss of function mutations in tumor suppressor genes R. Ghosh, S. Plon O37 Identification and electronic health record incorporation of clinically actionable pharmacogenomic variants using prospective targeted sequencing S. Scherer, X. Qin, R. Sanghvi, K. Walker, T. Chiang, D. Muzny, L. Wang, J. Black, E. Boerwinkle, R. Weinshilboum, R. Gibbs O38 Melanoma reprogramming state correlates with response to CTLA-4 blockade in metastatic melanoma T. Karpinets, T. Calderone, K. Wani, X. Yu, C. Creasy, C. Haymaker, M. Forget, V. Nanda, J. Roszik, J. Wargo, L. Haydu, X. Song, A. Lazar, J. Gershenwald, M. Davies, C. Bernatchez, J. Zhang, A. Futreal, S. Woodman O39 Data-driven refinement of complex disease classification from integration of heterogeneous functional genomics data in GeneWeaver E. J. Chesler, T. Reynolds, J. A. Bubier, C. Phillips, M. A. Langston, E. J. Baker O40 A general statistic framework for genome-based disease risk prediction M. Xiong, L. Ma, N. Lin, C. Amos O41 Integrative large-scale causal network analysis of imaging and genomic data and its application in schizophrenia studies N. Lin, P. Wang, Y. Zhu, J. Zhao, V. Calhoun, M. Xiong O42 Big data and NGS data analysis: the cloud to the rescue O. Dobretsberger, M. Egger, F. Leimgruber O43 Cpipe: a convergent clinical exome pipeline specialised for targeted sequencing S. Sadedin, A. Oshlack, Melbourne Genomics Health Alliance O44 A Bayesian classification of biomedical images using feature extraction from deep neural networks implemented on lung cancer data V. A. A. Antonio, N. Ono, Clark Kendrick C. Go O45 MAV-SEQ: an interactive platform for the Management, Analysis, and Visualization of sequence data Z. Ahmed, M. Bolisetty, S. Zeeshan, E. Anguiano, D. Ucar O47 Allele specific enhancer in EPAS1 intronic regions may contribute to high altitude adaptation of Tibetans C. Zeng, J. Shao O48 Nanochannel based next-generation mapping for structural variation detection and comparison in trios and populations H. Cao, A. Hastie, A. W. Pang, E. T. Lam, T. Liang, K. Pham, M. Saghbini, Z. Dzakula O49 Archaic introgression in indigenous populations of Malaysia revealed by whole genome sequencing Y. Chee-Wei, L. Dongsheng, W. Lai-Ping, D. Lian, R. O. Twee Hee, Y. Yunus, F. Aghakhanian, S. S. Mokhtar, C. V. Lok-Yung, J. Bhak, M. Phipps, X. Shuhua, T. Yik-Ying, V. Kumar, H. Boon-Peng O50 Breast and ovarian cancer prevention: is it time for population-based mutation screening of high risk genes? I. Campbell, M.-A. Young, P. James, Lifepool O53 Comprehensive coverage from low DNA input using novel NGS library preparation methods for WGS and WGBS C. Schumacher, S. Sandhu, T. Harkins, V. Makarov O54 Methods for large scale construction of robust PCR-free libraries for sequencing on Illumina HiSeqX platform H. DoddapaneniR. Glenn, Z. Momin, B. Dilrukshi, H. Chao, Q. Meng, B. Gudenkauf, R. Kshitij, J. Jayaseelan, C. Nessner, S. Lee, K. Blankenberg, L. Lewis, J. Hu, Y. Han, H. Dinh, S. Jireh, K. Walker, E. Boerwinkle, D. Muzny, R. Gibbs O55 Rapid capture methods for clinical sequencing J. Hu, K. Walker, C. Buhay, X. Liu, Q. Wang, R. Sanghvi, H. Doddapaneni, Y. Ding, N. Veeraraghavan, Y. Yang, E. Boerwinkle, A. L. Beaudet, C. M. Eng, D. M. Muzny, R. A. Gibbs O56 A diploid personal human genome model for better genomes from diverse sequence data K. C. C. Worley, Y. Liu, D. S. T. Hughes, S. C. Murali, R. A. Harris, A. C. English, X. Qin, O. A. Hampton, P. Larsen, C. Beck, Y. Han, M. Wang, H. Doddapaneni, C. L. Kovar, W. J. Salerno, A. Yoder, S. Richards, J. Rogers, J. R. Lupski, D. M. Muzny, R. A. Gibbs O57 Development of PacBio long range capture for detection of pathogenic structural variants Q. Meng, M. Bainbridge, M. Wang, H. Doddapaneni, Y. Han, D. Muzny, R. Gibbs O58 Rhesus macaques exhibit more non-synonymous variation but greater impact of purifying selection than humans R. A. Harris, M. Raveenedran, C. Xue, M. Dahdouli, L. Cox, G. Fan, B. Ferguson, J. Hovarth, Z. Johnson, S. Kanthaswamy, M. Kubisch, M. Platt, D. Smith, E. Vallender, R. Wiseman, X. Liu, J. Below, D. Muzny, R. Gibbs, F. Yu, J. Rogers O59 Assessing RNA structure disruption induced by single-nucleotide variation J. Lin, Y. Zhang, Z. Ouyang P1 A meta-analysis of genome-wide association studies of mitochondrial dna copy number A. Moore, Z. Wang, J. Hofmann, M. Purdue, R. Stolzenberg-Solomon, S. Weinstein, D. Albanes, C.-S. Liu, W.-L. Cheng, T.-T. Lin, Q. Lan, N. Rothman, S. Berndt P2 Missense polymorphic genetic combinations underlying down syndrome susceptibility E. S. Chen P4 The evaluation of alteration of ELAM-1 expression in the endometriosis patients H. Bahrami, A. Khoshzaban, S. Heidari Keshal P5 Obesity and the incidence of apolipoprotein E polymorphisms in an assorted population from Saudi Arabia population K. K. R. Alharbi P6 Genome-associated personalized antithrombotical therapy for patients with high risk of thrombosis and bleeding M. Zhalbinova, A. Akilzhanova, S. Rakhimova, M. Bekbosynova, S. Myrzakhmetova P7 Frequency of Xmn1 polymorphism among sickle cell carrier cases in UAE population M. 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Abduljaleel P13 Digital expression profiling of Purkinje neurons and dendrites in different subcellular compartments A. Kratz, P. Beguin, S. Poulain, M. Kaneko, C. Takahiko, A. Matsunaga, S. Kato, A. M. Suzuki, N. Bertin, T. Lassmann, R. Vigot, P. Carninci, C. Plessy, T. Launey P14 The evolution of imperfection and imperfection of evolution: the functional and functionless fractions of the human genome D. Graur P16 Species-independent identification of known and novel recurrent genomic entities in multiple cancer patients J. Friis-Nielsen, J. M. Izarzugaza, S. Brunak P18 Discovery of active gene modules which are densely conserved across multiple cancer types reveal their prognostic power and mutually exclusive mutation patterns B. S. Soibam P19 Whole exome sequencing of dysplastic leukoplakia tissue indicates sequential accumulation of somatic mutations from oral precancer to cancer D. Das, N. Biswas, S. Das, S. Sarkar, A. Maitra, C. Panda, P. Majumder P21 Epigenetic mechanisms of carcinogensis by hereditary breast cancer genes J. J. Gruber, N. Jaeger, M. Snyder P22 RNA direct: a novel RNA enrichment strategy applied to transcripts associated with solid tumors K. Patel, S. Bowman, T. Davis, D. Kraushaar, A. Emerman, S. Russello, N. Henig, C. Hendrickson P23 RNA sequencing identifies gene mutations for neuroblastoma K. Zhang P24 Participation of SFRP1 in the modulation of TMPRSS2-ERG fusion gene in prostate cancer cell lines M. Rodriguez-Dorantes, C. D. Cruz-Hernandez, C. D. P. Garcia-Tobilla, S. Solorzano-Rosales P25 Targeted Methylation Sequencing of Prostate Cancer N. Jäger, J. Chen, R. Haile, M. Hitchins, J. D. Brooks, M. Snyder P26 Mutant TPMT alleles in children with acute lymphoblastic leukemia from México City and Yucatán, Mexico S. Jiménez-Morales, M. Ramírez, J. Nuñez, V. Bekker, Y. Leal, E. Jiménez, A. Medina, A. Hidalgo, J. Mejía P28 Genetic modifiers of Alström syndrome J. Naggert, G. B. Collin, K. DeMauro, R. Hanusek, P. M. Nishina P31 Association of genomic variants with the occurrence of angiotensin-converting-enzyme inhibitor (ACEI)-induced coughing among Filipinos E. M. Cutiongco De La Paz, R. Sy, J. Nevado, P. Reganit, L. Santos, J. D. Magno, F. E. Punzalan , D. Ona , E. Llanes, R. L. Santos-Cortes , R. Tiongco, J. Aherrera, L. Abrahan, P. Pagauitan-Alan; Philippine Cardiogenomics Study Group P32 The use of “humanized” mouse models to validate disease association of a de novo GARS variant and to test a novel gene therapy strategy for Charcot-Marie-Tooth disease type 2D K. H. Morelli, J. S. Domire, N. Pyne, S. Harper, R. Burgess P34 Molecular regulation of chondrogenic human induced pluripotent stem cells M. A. Gari, A. Dallol, H. Alsehli, A. Gari, M. Gari, A. Abuzenadah P35 Molecular profiling of hematologic malignancies: implementation of a variant assessment algorithm for next generation sequencing data analysis and clinical reporting M. Thomas, M. Sukhai, S. Garg, M. Misyura, T. 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    The Improved Method and Device for Nucleic Acid Isolation Using a High-Salt Gel Electroelution Trap

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    The success of DNA analytical methods, including long-read sequencing, depends on the availability of high-quality, purified DNA. Previously, we developed a method and device for isolating high-molecular-weight (HMW) DNA for long-read sequencing using a high-salt gel electroelution trap. Here, we present an improved version of this method for purifying nucleic acids with higher yield and purity from even the most difficult biological samples. The proposed method is a significant improvement over the previously published procedure, offering a simple, fast, and efficient solution for isolating not only HMW DNA but also smaller DNA and RNA molecules. The method utilizes vertical gel electrophoresis in two nested, partially overlapping electrophoretic columns. The upper, smaller-diameter column has a thin layer of agarose gel at the bottom and electrophoresis buffer on top and serves to separate nucleic acids from impurities. After the target nucleic acid has been gel-purified on the upper column, a larger-diameter column with a layer of high-salt gel overlaid with electrophoresis buffer is inserted from below. The purified nucleic acid is then electroeluted into the buffer-filled gap between the separating gel and the high-salt gel, where excess counterions from the high-salt gel slow its migration and cause it to accumulate. The proposed vertical purification system outperforms the previously described horizontal system in terms of nucleic acid yield and purity, while also being more user-friendly, scalable, and adaptable to high-throughput workflows. Furthermore, the vertical system allows for the sequential purification of multiple nucleic acid species from the same sample using interchangeable salt-gel columns.Peer reviewe
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