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Showing 1 - 20 results of 193 for search '(( significant sequencing based ) OR ( significant ((old decrease) OR (mean decrease)) ))', query time: 0.11s Refine Results
  1. 1

    VEGAWES: variational segmentation on whole exome sequencing for copy number detection by Samreen Anjum (19651882)

    Published 2015
    “…<p dir="ltr">Copy number variations are important in the detection and progression of significant tumors and diseases. Recently, Whole Exome Sequencing is gaining popularity with copy number variations detection due to low cost and better efficiency. …”
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    Novel algorithms for accurate DNA base-calling by Mohammed, Omniyah Gul

    Published 2013
    “…The importance of DNA sequencing necessitated a need for efficient automation of identification of base sequences from traces generated by existing sequencing machines, a process referred to as DNA base-calling. …”
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    The Prevalence and Genetic Spectrum of Familial Hypercholesterolemia in Qatar Based on Whole Genome Sequencing of 14,000 Subjects by Ilhame Diboun (3522413)

    Published 2022
    “…This pioneering study provides a reliable estimate of FH prevalence in Qatar based on a significantly large population-based cohort, whilst uncovering the spectrum of genetic variants associated with FH.…”
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    Whole-genome Sequences of Multidrug-Resistant Escherichia coli by Khodor, Ragheed R.

    Published 2023
    “…In this study, we performed a whole-genome sequence-based analysis to understand the molecular epidemiology of multidrug-resistant E. coli clinical isolates. …”
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    masterThesis
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    Whole-genome sequencing based molecular characterization of multi-drug resistant isolates of Enterobacter spp. and Klebsiella aerogenes in Lebanon. (c2019) by Merhi, Georgi S.

    Published 2019
    “…Results were further confirmed through complimentary PCR assays and plasmid-based replicon typing (PBRT). Phylogenetic relatedness was assessed through whole-genome average nucleotide identity (wgANI) and core-genome single nucleotide polymorphism (cgSNP) based phylogenetic analysis. …”
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    masterThesis
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    Notch Signaling Inhibition by LY411575 Attenuates Osteoblast Differentiation and Decreased Ectopic Bone Formation Capacity of Human Skeletal (Mesenchymal) Stem Cells by Nihal AlMuraikhi (6002234)

    Published 2019
    “…Among the tested molecules, LY411575, a potent γ-secretase and Notch signaling inhibitor, exhibited significant inhibitory effects on osteoblastic differentiation of hBMSCs manifested by reduced ALP activity, mineralized matrix formation, and decreased osteoblast-specific gene expression as well as in vivo ectopic bone formation. …”
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    Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability by Farah R. Zahir (18892108)

    Published 2017
    “…The <i>de novo</i> assembly resulted in unmasking hidden genome instability that was missed by standard re-alignment based algorithms. We also interrogated regulatory sequence variation for known and hypothesized ID genes and present useful strategies for WGS data analyses for non-coding variation.…”
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    Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene by Zalloua, Pierre

    Published 2004
    “…The GG genotype was also significantly higher among patients (12.6%) than in controls (4.2%). χ2 analysis and family-based association studies were performed and suggested the association of CTLA4 exon 1 G polymorphism with T1D (p = 0.0229). …”
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    Morphological changes in amblyopic eyes in choriocapillaris and Sattler’s layer in comparison to healthy eyes, and in retinal nerve fiber layer in comparison to fellow eyes through... by Masri, Oussama Samer

    Published 2021
    “…Results The method of measuring reflectivity is good to excellent reliability for all regions of interest except the fourth. The mean reflectivity of the choriocapillaris and Sattler’s layer in amblyopic eyes were significantly lower than in healthy eyes (p = 0.003 and p = 0.008 respectively). …”
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    Novel metal–organic framework biosensing platform for detection of COVID-19 RNA by Elgazar, Aya

    Published 2024
    “…This research aims to develop a Zeolitic Imidazolate Framework-8 (ZIF-8) based fluorescent biosensor for facile and rapid COVID-19 RNA sequence detection. …”
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    Temporal fusion transformer-based prediction in aquaponics by Ahmet Metin (12832543)

    Published 2023
    “…Experimental results demonstrate significant improvements of the proposed model over baseline models in terms of MAE, MSE, and Explained Variance metrics considering one-hour sequences. …”
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    Metaheuristic Algorithm for State-Based Software Testing by Haraty, Ramzi A.

    Published 2018
    “…SA evolves a solution by minimizing an energy function that is based on testing objectives such as coverage, diversity, and continuity of events. …”
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    A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family by Safeer Ahmad (9079257)

    Published 2023
    “…</i></p><h3>Methods</h3><p dir="ltr">Clinical and radiological studies were performed to determine the phenotypic spectrum and hormonal profile of the disease, while whole-exome sequencing (WES) and Sanger sequencing were performed to identify the disease-causing mutation. …”