Robust Preamble-Based Timing Synchronization for OFDM Systems

This study presents a novel preamble-based timing offset estimation method for orthogonal frequency division multiplexing (OFDM) systems. The proposed method is robust, immune to the carrier frequency offset (CFO), and independent of the structure of the preamble. The performance of the new method is demonstrated in terms of mean square error (MSE) obtained by simulation in multipath fading channels. The results indicate that the new method significantly improves timing performance in comparison with existing methods

Sequencing and analysis of the complete mitochondrial genome of Mansonia uniformis (Dipera: Culicidae)

In this study, we sequenced and analyzed the complete mitochondrial genome of Mansonia uniformis, and this is the first report on the genus Mansonia. The circular mitogenome is 15,603 bp long and contains 13 protein-coding genes (PCGs), 22 tRNA genes, 2 ribosomal RNA genes, and a A + T-rich control region. Most PCGs start with ATN codons, and end with TAA, except for COX1 starting with TCG codons and COX2 ending with a single thymine stop codon. The phylogenetic tree based on the COX1 gene showed that M. uniformis formed a monophyletic clade, sister to other seven genus from the subfamily Culicinae

Robust Preamble-Based Timing Synchronization for OFDM Systems

This study presents a novel preamble-based timing offset estimation method for orthogonal frequency division multiplexing (OFDM) systems. The proposed method is robust, immune to the carrier frequency offset (CFO), and independent of the structure of the preamble. The performance of the new method is demonstrated in terms of mean square error (MSE) obtained by simulation in multipath fading channels. The results indicate that the new method significantly improves timing performance in comparison with existing methods

Near-Infrared Fluorescent Probe for Detection of Thiophenols in Water Samples and Living Cells

The development of probes for rapid, selective, and sensitive detection of the highly toxic thiophenols is of great importance in both environmental and biological science. Despite the appealing advantages of near-infrared (NIR) fluorescent detection, no NIR fluorescent probes have been reported for thiophenols to date. Using the chemical properties of thiophenols that are able to cleave sulfonamide selectively and efficiently under mild conditions, we herein report a dicyanomethylene-benzopyran (DCMB)-based NIR fluorescent probe for thiophenols. This probe features remarkable large Stokes shift and shows a rapid, highly selective, and sensitive detection process for thiophenols with significant NIR fluorescent turn-on responses. The potential applications of this new NIR fluorescent probe were demonstrated by the quantitative detection of thiophenol in real water samples and by fluorescent imaging of thiophenol in living cells

Rapid and Ratiometric Fluorescent Detection of Cysteine with High Selectivity and Sensitivity by a Simple and Readily Available Probe

We report a simple and readily available fluorescent probe for rapid, specific, and ratiometric fluorescent detection of the biologically important cysteine (Cys). This probe uses a visible-light excitable excited-state intramolecular proton transfer (ESIPT) dye (4′-dimethylamino-3-hydroxyflavone) as the fluorophore and an acrylate group as the ESIPT blocking agent as well as the recognition unit. Cleavage of the acrylate moiety can be achieved specifically and rapidly by Cys in aqueous solution under mild conditions, which leads to restore the ESIPT process and enables the probe to show a rapid, ratiometric fluorescent detection process for Cys with high selectivity over various analytes, including homocysteine (Hcy) and glutathione (GSH). The detection limit of this probe for Cys was found to be ∼0.2 μM and bioimaging of intracellular Cys by this probe was successfully applied in living cells, indicating that this probe holds great potential for biological applications