336 research outputs found

    Photosynthetic Pigments Content of Trapa Natans Specie in Skadar Lake

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    Skadar lake is the largest lake in th Balkan Peninsula. The total area is 5500 m². Terretorialy the lake belong to Montenegro and to Albania. Both the sides of lake is a big development of acquatic vegetation, including a large variety of habitats and biological communities. The most important associations are Potameto-Najadetum, Trapetum natantis, Myriophyllo-Nupharetum, Nymphoideum peltata. These associations include lake shore macrophytes Najas, Vallisneria, Potamogeton, floating macrophytes Nuphar luteum, Trapa natans, Numphaea alba. Emersed water macrophytes are developed on both sides of lake predominantly in the eastern part of lake (Kamice Shegan) which go as far as 3 meter deep such Ceratophyllum, Najas marina, Najas minor, Vallisneria.Trapeum natantisi is largely widespread community in the Skadar lake. Waternuts develops wide population and communities in the inner and deeper part of the floating macrophyta zones. Plant samples were collected on the both sides of the lake. For Trapa natans specie is determined the content of photosynthetic pigments, chlorophyll a, chlorophyll b and carotenoids. Photosynthetic pigments were extracted with 80% acetone and their concentrations are expressed in mg/g dry absolutely leaf .Their measurement is made in the bands f 663, 645.470, of spectriphotometer. Trapa natans was found in the eastern shore and in western shore of Skadar lake. The highest values of chlorophyll a an b in the species Trapa natans was found in September 2014

    Opportunistic zoster non HIV-related

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    Microsatellite linkage analysis, single-nucleotide polymorphisms, and haplotype associations with ECB21 in the COGA data

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    This study, part of the Genetic Analysis Workshop 14 (GAW14), explored real Collaborative Study on the Genetics of Alcoholism data for linkage and association mapping between genetic polymorphisms (microsatellite and single-nucleotide polymorphisms (SNPs)) and beta (16.5–20 Hz) oscillations of the brain rhythms (ecb21). The ecb21 phenotype underwent the statistical adjustments for the age of participants, and for attaining a normal distribution. A total of 1,000 subjects' available phenotypes were included in linkage analysis with microsatellite markers. Linkage analysis was performed only for chromosome 4 where a quantitative trait locus with 5.01 LOD score had been previously reported. Previous findings related this location with the γ-aminobutyric acid type A (GABA(A)) receptor. At the same location, our analysis showed a LOD score of 2.2. This decrease in the LOD score is the result of a drastic reduction (one-third) of the available GAW14 phenotypic data. We performed SNP and haplotype association analyses with the same phenotypic data under the linkage peak region on chromosome 4. Seven Affymetrix and two Illumina SNPs showed significant associations with ecb21 phenotype. A haplotype, a combination of SNPs TSC0044171 and TSC0551006 (the latter almost under the region of GABA(A )genes), showed a significant association with ecb21 (p = 0.015) and a relatively high frequency in the sample studied. Our results affirmed that the GABA region has potential of harboring genes that contribute quantitatively to the beta oscillation of the brain rhythms. The inclusion of the remaining 614 subjects, which in the GAW14 had missing data for the ecb21, can improve the strength of the associations as they have already shown that they contribute quite important information in the linkage analysis

    Use of a random coefficient regression (RCR) model to estimate growth parameters

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    We used a random coefficient regression (RCR) model to estimate growth parameters for the time series of observed serum glucose levels in the Replicate 1 of the Genetic Analysis Workshop 13 simulated data. For comparison, a two time-point interval was also selected and the slope between these two observations was calculated. This process yielded four phenotypes: the RCR growth phenotype, a two time-point slope phenotype, and Time 1 and Time 2 serum glucose level phenotypes. These four phenotypes were used for linkage analyses on simulated chromosomes 5, 7, 9, and 21, those chromosomes that contained loci affecting the growth course for serum glucose levels. The linkage analysis of the RCR-derived phenotype showed overwhelming evidence for linkage at one locus (LOD 65.78 on chromosome 5), while showing elevated but nonsignificant LOD scores for two other loci (LOD 1.25 on chromosome 7, LOD 1.10 on chromosome 9), and no evidence of linkage for the final locus. The two time-point slope phenotype showed evidence for linkage at one locus (LOD 4.16 on chromosome 5) but no evidence for linkage at any of the other loci. A parallel cross-sectional approach, using as input phenotypes the endpoints of the two-point slope phenotype, gave strong linkage results for the major locus on chromosome 5 (maximal LOD scores of 17.90 and 27.24 for Time 1 and Time 2, respectively) while showing elevated but nonsignificant linkage results on chromosome 7 (maximal LOD scores of 1.71 and 1.48) and no evidence for linkage at the two remaining loci. The RCR growth parameter showed more power to detect linkage to the major locus than either the cross-sectional or two-point slope approach, but the cross-sectional approach gave a higher maximal LOD score for one of the minor loci

    Distance-based phenotypic association analysis of DNA sequence data

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    As the cost of sequencing decreases, the demand for association tests that use exhaustive DNA sequence information increases. One such association test is multivariate distance matrix regression (MDMR). We explore some of the features of MDMR using Genetic Analysis Workshop 17 simulated data in search of potential improvements in distance measures. We used genotype data from 697 unrelated individuals, in 200 replications, to test the power of MDMR to detect 13 trait Q2 causative genes based on the Euclidean distance metric. We also estimated the false-positive rate of MDMR using 508 control genes. In addition, we compared MDMR with Mantel’s test and collapsing analysis for rare variants. MDMR performed comparably well even with the Euclidean distance measure
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