A new class of functions is defined by expressing analytic characterizations of starlike function involving logarithm. To make this study more versatile, we redefine and study the class involving an operator associated with -hypergeometric function. Estimates of the initial coefficients and Fekete-Szegő inequality of the functions, which belong to the defined function class, are our main results.
While academic literature offers various models of tourism competitiveness, their specific application to sports tourism in the unique contexts of developing nations remains fragmented and under-theorized, with no prior systematic mapping of evidence from these settings. This scoping review protocol outlines a systematic methodology to comprehensively map and synthesize the existing literature on the competitiveness of sports tourism destinations, with a specific focus on evidence from developing countries. The primary research question is: What are the key determinants and conceptualizations of competitiveness for sports tourism destinations in developing countries? Guided by the Joanna Briggs Institute (JBI) Scoping Review Framework and reported per PRISMA-ScR guidelines, the review will employ inclusive eligibility criteria (Population: sports tourism destinations; Concept: competitiveness factors; Context: developing countries), search academic and grey literature sources, extract data on definitions, determinants, models, challenges, strategies, and evidence, and conduct inductive thematic analysis to identify patterns and gaps. The findings aim to consolidate existing knowledge, identify key determinants and gaps, and establish a foundational understanding to guide future research, policy formulation, and industry practices in the sports tourism domain, particularly for resource-constrained settings.
Optical Genome Mapping (OGM) is an emerging technology in clinical laboratories for identifying copy number and structural variations in the DNA of patients with haematological malignancies. A critical initial step is the isolation of ultra-high molecular weight genomic DNA (UHMW gDNA), which typically requires 1.5 million white blood cells. However, this cell number is not always achievable in clinical practice due to various limitations. For instance, diagnostic analysis of multiple myeloma (MM) is should be performed on CD138-positive cells derived from bone marrow aspirates (BMA), where both the sample volume and the number of CD138-positive cells This method describes a customized protocol which enables isolation of UHMW gDNA starting from as few as 500 000 cells, while still resulting in DNA of sufficient quality and quantity to perform OGM and collect at least 1500 Gbp of data.

