33 research outputs found

    GOEMAI/ANKWEI RELIGIOSITY: UNDERSTANDING INDIGENOUS DIVINITY IN RELATION TO CHRISTIANITY

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    Postcolonial/decolonial thinking developed in response to modernity’s colonial logic that glorified and universalized the Western locus of enunciation, subjectivity, and history. The prioritization of Western epistemology, hierarchization of being based on race, gender, and religion, and the universalization of Western Christian religion relegated all other modes of being, knowing, and accessing the Divine to the periphery. For a long time, indigenous people have accepted the Western linear worldview that makes them the exemplars of the whites (Euro-Americans) in their primordial state of Western history and development. The goal of the Western colonial matrix of power is the subsumption of indigenous cosmology into its universalized cosmogony, aligning every reality into a single mode of understanding and interpretation. It is that “point zero,” viz., the particular perspective that refuses to acknowledge that fact but assumes the “god’s-eye view” concerning everything. The desire for self-apprehension, retrieval, relinking, and reconnection to the indigenous worldview necessitated the rejection of Western temporality for indigenous spatiality. Spatiality prioritizes experience and context over the progressive idea of time in history. While rationality defines the Western universe, relationality characterizes the indigenous world. This work takes for its context the Goemai space and experience to argue for a deconstruction of Western epistemology, mode of being, and Christianity. It posits that the search for a genuine Goemai Christianity that is fully Catholic is at the base of retrieving ancestral wisdom and experience to construct a future from the present by looking backward

    Identification of Selected Kinetoplastids 18S rRNA Residues required for Efficient Recruitment of Initiator tRNA Met and AUG Selection in silico

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    High Resolution 18S rRNA structures of kinetoplastids ribosomes from theoretical methods have provided atomic level details about the process of translation. This process entails detailed information on the mRNA and tRNA binding and decoding centers within the 18S rRNA that was previously not very well understood. We identified residues in selected kinetoplastids 18S rRNA critical in recruiting the first methionyl tRNA to the small ribosome subunit during initiation and comparing them to see the differences. The Kozak sequence presence on eukaryotic mRNAs tethers it to the AUG start codon. Kinetoplastids are a closely related group, and the three chosen exhibited differences in the A-site in terms of position and nucleotides found there. Interactions are found at the A-site (543-UUU-546 for T. cruzi, 560-CCUA-563 for T. brucei, and 540-UUUG-543 for Leishmania major), where the different mRNA get complementary sequences at the 16th helix. The current findings show that each messenger RNA has a sequence that is complementary to the appropriate 18S rRNA sequence, tethering the mRNA to the small ribosomal subunit, which then recruits the bigger subunit. When compared to the Kozak region that flanks the AUG start codon, this method effectively promotes start codon placement

    Comprehensive transcriptome of the maize stalk borer, Busseola fusca, from multiple tissue types, developmental stages, and parasitoid wasp exposures

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    Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

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    Despite rapid technical progress and demonstrable effectiveness for some types of diagnosis and therapy, much remains to be learned about clinical genome and exome sequencing (CGES) and its role within the practice of medicine. The Clinical Sequencing Exploratory Research (CSER) consortium includes 18 extramural research projects, one National Human Genome Research Institute (NHGRI) intramural project, and a coordinating center funded by the NHGRI and National Cancer Institute. The consortium is exploring analytic and clinical validity and utility, as well as the ethical, legal, and social implications of sequencing via multidisciplinary approaches; it has thus far recruited 5,577 participants across a spectrum of symptomatic and healthy children and adults by utilizing both germline and cancer sequencing. The CSER consortium is analyzing data and creating publically available procedures and tools related to participant preferences and consent, variant classification, disclosure and management of primary and secondary findings, health outcomes, and integration with electronic health records. Future research directions will refine measures of clinical utility of CGES in both germline and somatic testing, evaluate the use of CGES for screening in healthy individuals, explore the penetrance of pathogenic variants through extensive phenotyping, reduce discordances in public databases of genes and variants, examine social and ethnic disparities in the provision of genomics services, explore regulatory issues, and estimate the value and downstream costs of sequencing. The CSER consortium has established a shared community of research sites by using diverse approaches to pursue the evidence-based development of best practices in genomic medicine

    Realization of a Joint MIMO Radar and Communication System using a PSK-LFM Waveform

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    In this paper, a new technique which enables communication data to be embedded into MIMO radar waveform is presented. A linear frequency modulated (LFM) signal is used for radar sensing, and multiple phase shift keying (PSK) symbols, for communications, are embedded into the LFM signal. In this way, multiple communication symbols per radar pulse are generated. Such waveforms are subsequently combined within a multiple-input multiple-output (MIMO) configuration. Orthogonality between transmitters is ensured using time-division multiplexing (TDM). The performance of this novel PSK-LFM technique is demonstrated through both simulation and experimentation.</p

    Development and Sensory Evaluation of Omega-3-Rich Nile Perch Fish Oil-Fortified Yogurt

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    Nile perch (Lates niloticus) is a major fish species in East Africa and its processing produces sufficient amounts of by-products containing significant amounts of long-chain polyunsaturated fatty acids (PUFAs). Due to the health benefits associated with PUFAs, they can be incorporated into commonly consumed foods such as yoghurt. This study is aimed at developing an omega-3-rich functional yoghurt and evaluating its quality and acceptability. Omega-3-rich fish oils were obtained from Nile perch fat pads in the presence and absence of a commercial food grade enzyme Alcalase. Recovery of omega-3-rich fish oil was done by centrifugation at 1000×g at room temperature. The peroxide value (PV), anisidine value (AV), total oxidation (TOTOX), and free fatty acids (FFA) were some of the quality parameters investigated. Natural yoghurt (150 ml) was prepared and spiked with 3.5 g of omega-3-rich Nile perch oil. To mask the fishy flavor and taste, four different flavors were used and sensory evaluation of the yoghurt samples was performed. The liberation of Nile perch fish oil in the absence of Alcalase gave better yield (60.7% wet weight), while the use of Alcalase gave lower yields (48.3% wet weight). Assessment of the quality of the extracted fish oils showed that all parameters were within the required limits. Sensory characterization by a panel of students showed that passion and strawberry flavors were the most liked with mean values of 4.65 and 4.625, respectively. This study revealed that substantial amounts of omega-3-rich fish oil can be extracted from Nile perch fish pads in the absence of exogenous enzymes. Fortification of yoghurt with omega-3-rich Nile perch fish oils is an approach towards increasing omega-3 intake within the Kenyan population and globally
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