Metaheuristics Techniques for Cluster Head Selection in WSN: A Survey

In recent years, Wireless sensor communication is growing expeditiously on the capability to gather information, communicate and transmit data effectively. Clustering is the main objective of improving the network lifespan in Wireless sensor network. It includes selecting the cluster head for each cluster in addition to grouping the nodes into clusters. The cluster head gathers data from the normal nodes in the cluster, and the gathered information is then transmitted to the base station. However, there are many reasons in effect opposing unsteady cluster head selection and dead nodes. The technique for selecting a cluster head takes into factors to consider including residual energy, neighbors’ nodes, and the distance between the base station to the regular nodes. In this study, we thoroughly investigated by number of methods of selecting a cluster head and constructing a cluster. Additionally, a quick performance assessment of the techniques' performance is given together with the methods' criteria, advantages, and future directions

Genetic diversity fuels gene discovery for tobacco and alcohol use.

Tobacco and alcohol use are heritable behaviours associated with 15% and 5.3% of worldwide deaths, respectively, due largely to broad increased risk for disease and injury. These substances are used across the globe, yet genome-wide association studies have focused largely on individuals of European ancestries. Here we leveraged global genetic diversity across 3.4 million individuals from four major clines of global ancestry (approximately 21% non-European) to power the discovery and fine-mapping of genomic loci associated with tobacco and alcohol use, to inform function of these loci via ancestry-aware transcriptome-wide association studies, and to evaluate the genetic architecture and predictive power of polygenic risk within and across populations. We found that increases in sample size and genetic diversity improved locus identification and fine-mapping resolution, and that a large majority of the 3,823 associated variants (from 2,143 loci) showed consistent effect sizes across ancestry dimensions. However, polygenic risk scores developed in one ancestry performed poorly in others, highlighting the continued need to increase sample sizes of diverse ancestries to realize any potential benefit of polygenic prediction