82 research outputs found

    Optimal Resource Deployment in an Infostation-Based Network

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    This paper considers the problem of finding an optimal deployment of information resources on an InfoStation network in order to minimize the overhead and reduce the time needed to satisfy user requests for resources. The RG-Optimization problem and an approach for its solving are presented as well

    Power-line Interference Removal from ECG in Case of Power-line Frequency Variations

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    The original version of the most successful approach for power-line (PL) interference removal from ECG, called subtraction procedure, is based on linear segment detection in the signal and hardware synchronised analogue-to-digital conversion to cope with the PL frequency variations. However, this is not feasible for battery supplied devices and some computer-aided ECG systems. Recent improvements of the procedure apply software measurement of the frequency variations that allow a re-sampling of the contaminated signal with the rated PL frequency followed by interference removal and back re-sampling for restoration of the original time intervals. This study deals with a more accurate software frequency measurement and introduces a notch filtration as alternative to the procedure when no linear segments are encountered for long time, e.g. in cases of ventricular fibrillation or tachycardia. The result obtained with large PL frequency variations demonstrate very small errors, usually in the range of Β± 20 ΞΌV for the subtraction procedure and Β± 60 ΞΌV for the notch filtration, the last values strongly depending on the frequency contents of the QRS complexes

    Development of molecular microfluidic devices for bio-analytical sensors

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    Continuously Tested and Used QRS Detection Algorithm: Free Access to the MATLAB Code

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    Each ECG analysis begins with the detection of the QRS complex, which is the most distinguishable wave for initial investigation. Long ago we published an algorithm for ventricular beats (VB) detection in single ECG lead. The classification of normal QRS complexes is based on the slope, the amplitude and the width of the ECG waves. Other criteria recognize ventricular ectopic beats (EB) by presence of biphasic beats and separate premature EB from the already detected QRS complexes. The aim of this paper is to place the MATLAB program of our algorithm at disposal to the readers (http://www.biomed.bas.bg/bioautomation/2019/vol_23.1/files/23.1_06.zip) looking forward to more successful ECG investigations

    SMILE Maker:a web-based tool for problem solving

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    This paper focuses on the purposes, theoretical model, and functionality of the SMILE (Solution Mapping Intelligent Learning Environment) Maker--a World Wide Web-based problem-solving tool. From an instructional design point of view, an attempt to establish a balance between constructivism/instructivism, content-treatment interaction/aptitude-treatment interaction, and user locus of control/system locus of control is made. The model behind the SMILE Maker consists of four sub-models (user, content, instructional events, and facilitator), each built from four components. A new concept mapping method that has been developed and experimentally validated is described. Four instructional scenarios--ready-made, tailor-made, self-made, and atelier--are discussed

    Aloenzimna genetichna harakteristika na pchelni semeystva Apis mellifera (Hymenoptera: Apidae) ot Bulgaria s razlichno higienno povedenie

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    The genetic variability in 25 honey bee colonies from different regions of Bulgaria with different hygienic behaviour (highly hygienic, hygienic and non-hygienic) has been studied. Alloenzyme analysis of two systems (MDH-1 and Est-3) corresponding to 2 loci was used in order to characterize the colony polymorphism. Totally 1,150 worker bees were included in this investigation. MDH-1 locus was found to be polymorphic in all of the studied colonies, having two alleles – MDH-165 and MDH-1100. The Est-3 locus was fixed in ten of the investigated colonies. Polymorphism with total presence of four alleles of this locus (Est-380, Est-388, Est-3100 and Est-3118) was found in the other studied colonies. The calculated polymorphism was 50% in the non-hygienic and 100% in the highly hygienic and hygienic colonies. The observed and expected heterozygosities (Ho and He) ranged from 0.296 to 0.354 and from 0.28 to 0.332 in non-hygienic and highly hygienic groups, respectively. The calculated mean observed and expected heterozygosities were 0.32 and 0.307, respectively. The calculated Fst and Nm levels demonstrated lower differentiation between highly hygienic and hygienic colonies and higher differentiation between highly hygienic and non-hygienic colonies. Dissimilarities between levels of polymorphism, heterozygosity, Fst, Nm and allele frequencies in the studied groups of colonies with different hygienic behaviour were found and discussed. The results of the present study provide new information concerning relations between hygienic behaviour and alloenzyme characteristics which could be used for future selection with honey bees in Bulgaria.Obekt na nastoyashtoto izsledvane e genetichnata izmenchivost, ustanovena pri rabota s 25 pchelni semeystva ot razlichni rayoni na Bulgaria s razlichno higienno povedenie (Visoko higienichni, higienichni i ne-higiennichni). Izyaveniyat polimorfizam e harakteriziran na bazata na aloenzimen analiz po dve sistemi (MDH-1 i Est-3), saotvetstvashti na dva polimorfni lokusa. Obshto 1150 pcheli rabotnichki sa vklyucheni v izsledvaneto. Ustanoveno e, che MDH-1 lokusat e polimorfen vav vsichki izsledvani pchelni semeystva i e predstaven ot dva alela - MDH-165 i MDH-1100. Est-3 lokusat e fiksiran v deset ot izsledvanite kolonii. Po tozi lokus e konstatiran polimorfizam s prisastvie obshto na chetiri alelni varianti (Est-380, Est-388, Est-3100 i Est-3118) za genofonda na ostanalite pchelni semeystva. Izchisleniyat polimorfizam e mezhdu 50% i 100%. Ustanovenata i ochakvanata heterozigotnost (Ho i He) varira saotvetno ot 0.296 do 0.354 i 0.28 ot 0.332 pri ne-higienichnite i visoko higienichnite grupi. Izchislenite sredna nablyudavana i ochakvana heterozigotnosti sa saotvetno 0.32 i 0.307. Izchislenite niva na Fst i Nm pokazvat po-niska diferentsiatsia mezhdu visoko higienichnite i higienichnite semeystva i visoka diferentsiatsia mezhdu visoko higienichnite i ne-higienichnite semeystva. Konstatirani i obsadeni sa razlichia mezhdu nivata na polimorfizam, heterozigotnost, Fst, Nm i alelnite chestoti v izsledvanite grupi pchelni semeystva s razlichno higienno povedenie. Rezultatite ot nastoyashtoto prouchvane davat nova informatsia otnosno zavisimostta mezhdu nivata na higienno povedenie i aloenzimnite harakteristiki, koito biha mogli da se izpolzvat v badeshti deynosti po selektsia na medonosnite pcheli v Bulgaria

    ΠœΠΈΡ‚ΠΎΠΈΠ½Ρ…ΠΈΠ±ΠΈΡ€Π°Ρ‰ ΠΈ кластогСнСн Π΅Ρ„Π΅ΠΊΡ‚ Π½Π° Π²ΠΎΠ΄ΠΈ ΠΎΡ‚ Π°Π½Ρ‚Ρ€ΠΎΠΏΠΎΠ³Π΅Π½Π½ΠΎ повлияни Π·ΠΎΠ½ΠΈ

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    The present study aims to analyse the effect of waters, anthropogenically influenced by various pollutants, on the mitotic division and chromosomal apparatus of cells by establishing their potential mitoinhibitory and clastogenic effect. The cytotoxic and mutagenic effect of contaminated water was examined by the application of the Allium cepa test system. Mitotic depression has been established for samples with available anthropogenic contamination. Microscopic analysis showed an increased incidence of chromosomal aberrations in the test samples compared to the control, resulting from the genotoxic effect available. Chromosomal abnormalities of the type of lagging and β€˜vagrant’ chromosomes, chromosomal fragments, anaphase and telophase bridges, micronuclei, as well as deviations from normal cell division such as K-mitoses and asynchronous mitoses have been observed. The analysis of the spectrum of chromosomal aberrations shows some differences in the frequency of occurrence of the different types of disorders, which reflects the specificity of the genotoxic effect of the water samples from the surveyed areas.Настоящото ΠΏΡ€ΠΎΡƒΡ‡Π²Π°Π½Π΅ ΠΈΠΌΠ° Π·Π° Ρ†Π΅Π» Π΄Π° Π°Π½Π°Π»ΠΈΠ·ΠΈΡ€Π° влияниСто Π½Π° Π°Π½Ρ‚Ρ€ΠΎΠΏΠΎΠ³Π΅Π½Π½ΠΎ повлияни ΠΎΡ‚ Ρ€Π°Π·Π»ΠΈΡ‡Π½ΠΈ Π·Π°ΠΌΡŠΡ€ΡΠΈΡ‚Π΅Π»ΠΈ Π²ΠΎΠ΄ΠΈ Π²ΡŠΡ€Ρ…Ρƒ ΠΌΠΈΡ‚ΠΎΡ‚ΠΈΡ‡Π½ΠΎΡ‚ΠΎ Π΄Π΅Π»Π΅Π½Π΅ ΠΈ хромозомния Π°ΠΏΠ°Ρ€Π°Ρ‚ Π½Π° ΠΊΠ»Π΅Ρ‚ΠΊΠΈΡ‚Π΅ Ρ‡Ρ€Π΅Π· установяванС Π½Π° потСнциалния ΠΈΠΌ ΠΌΠΈΡ‚ΠΎΠΈΠ½Ρ…ΠΈΠ±ΠΈΡ€Π°Ρ‰ ΠΈ кластогСнСн Π΅Ρ„Π΅ΠΊΡ‚ Π§Ρ€Π΅Π· ΠΏΡ€ΠΈΠ»Π°Π³Π°Π½Π΅ Π½Π° Allium cepa тСст-систСмата Π΅ ΠΏΡ€ΠΎΡƒΡ‡Π΅Π½ΠΎ цитотоксичното ΠΈ ΠΌΡƒΡ‚Π°Π³Π΅Π½Π½ΠΎΡ‚ΠΎ дСйствиС Π½Π° Π·Π°ΠΌΡŠΡ€ΡΠ΅Π½ΠΈΡ‚Π΅ Π²ΠΎΠ΄ΠΈ. ΠšΠΎΠ½ΡΡ‚Π°Ρ‚ΠΈΡ€Π°Π½Π° Π΅ ΠΌΠΈΡ‚ΠΎΡ‚ΠΈΡ‡Π½Π° дСпрСсия Π·Π° ΠΏΡ€ΠΎΠ±ΠΈΡ‚Π΅ с Π½Π°Π»ΠΈΡ‡Π½ΠΎ Π°Π½Ρ‚Ρ€ΠΎΠΏΠΎΠ³Π΅Π½Π½ΠΎ Π·Π°ΠΌΡŠΡ€ΡΡΠ²Π°Π½Π΅. ΠœΠΈΠΊΡ€ΠΎΡΠΊΠΎΠΏΡΠΊΠΈΡΡ‚ Π°Π½Π°Π»ΠΈΠ· ΠΏΠΎΠΊΠ°Π·Π²Π° ΡƒΠ²Π΅Π»ΠΈΡ‡Π΅Π½Π° чСстота Π½Π° Ρ…Ρ€ΠΎΠΌΠΎΠ·ΠΎΠΌΠ½ΠΈΡ‚Π΅ Π°Π±Π΅Ρ€Π°Ρ†ΠΈΠΈ Π² ΠΎΠΏΠΈΡ‚Π½ΠΈΡ‚Π΅ ΠΏΡ€ΠΎΠ±ΠΈ Π² сравнСниС с ΠΊΠΎΠ½Ρ‚Ρ€ΠΎΠ»Π½Π°Ρ‚Π°, ΠΊΠΎΠ΅Ρ‚ΠΎ Π΅ Ρ€Π΅Π·ΡƒΠ»Ρ‚Π°Ρ‚ ΠΎΡ‚ Π½Π°Π»ΠΈΡ‡Π΅Π½ гСнотоксичСн Π΅Ρ„Π΅ΠΊΡ‚. ΠšΠΎΠ½ΡΡ‚Π°Ρ‚ΠΈΡ€Π°Π½ΠΈ са Ρ…Ρ€ΠΎΠΌΠΎΠ·ΠΎΠΌΠ½ΠΈ Π°Π½ΠΎΠΌΠ°Π»ΠΈΠΈ ΠΎΡ‚ Ρ‚ΠΈΠΏΠ° Π½Π° изоставащи ΠΈ β€žΡΠΊΠΈΡ‚Π°Ρ‰ΠΈβ€ Ρ…Ρ€ΠΎΠΌΠΎΠ·ΠΎΠΌΠΈ, Ρ…Ρ€ΠΎΠΌΠΎΠ·ΠΎΠΌΠ½ΠΈ Ρ„Ρ€Π°Π³ΠΌΠ΅Π½Ρ‚ΠΈ, Π°Π½Π°Ρ„Π°Π·Π½ΠΈ ΠΈ Ρ‚Π΅Π»ΠΎΡ„Π°Π·Π½ΠΈ мостовС, микроядра, ΠΊΠ°ΠΊΡ‚ΠΎ ΠΈ отклонСния ΠΎΡ‚ Π½ΠΎΡ€ΠΌΠ°Π»Π½ΠΎΡ‚ΠΎ ΠΊΠ»Π΅Ρ‚ΡŠΡ‡Π½ΠΎ Π΄Π΅Π»Π΅Π½Π΅ ΠΊΠ°Ρ‚ΠΎ К-ΠΌΠΈΡ‚ΠΎΠ·ΠΈ ΠΈ асинхронни ΠΌΠΈΡ‚ΠΎΠ·ΠΈ. ΠΠ½Π°Π»ΠΈΠ·ΡŠΡ‚ Π½Π° ΡΠΏΠ΅ΠΊΡ‚ΡŠΡ€Π° Π½Π° Ρ…Ρ€ΠΎΠΌΠΎΠ·ΠΎΠΌΠ½ΠΈΡ‚Π΅ Π°Π±Π΅Ρ€Π°Ρ†ΠΈΠΈ ΠΏΠΎΠΊΠ°Π·Π²Π° извСстни различия Π² чСстотата Π½Π° срСщанС Π½Π° ΠΎΡ‚Π΄Π΅Π»Π½ΠΈΡ‚Π΅ Ρ‚ΠΈΠΏΠΎΠ²Π΅ Π½Π°Ρ€ΡƒΡˆΠ΅Π½ΠΈΡ, ΠΊΠΎΠ΅Ρ‚ΠΎ отразява спСцификата Π½Π° гСнотоксичното дСйствиС Π½Π° Π²ΠΎΠ΄Π½ΠΈΡ‚Π΅ ΠΏΡ€ΠΎΠ±ΠΈ ΠΎΡ‚ ΠΏΡ€ΠΎΡƒΡ‡Π²Π°Π½ΠΈΡ‚Π΅ Π·ΠΎΠ½ΠΈ
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