Synthesis of ultra-wideband (UWB) linear frequency modulation radar signals is a very important technology for microwave imaging, target identification and detection of low radar-cross-section (RCS) targets. A new...Synthesis of ultra-wideband (UWB) linear frequency modulation radar signals is a very important technology for microwave imaging, target identification and detection of low radar-cross-section (RCS) targets. A new method of UWB radar signals generation with two-channel signal generator is presented. The realization structure is given; the principle and errors of signal synthesis are analyzed. At the same time, an automatic .adjustment measure of signal phase is proposed because of phase discontinuity of waveform in this method. The simulation experiment and analysis results indicate that radar signals with large instantaneous bandwidth can be generated by means of this method on the condition that the high-speed digital devices are limited.展开更多
文摘Synthesis of ultra-wideband (UWB) linear frequency modulation radar signals is a very important technology for microwave imaging, target identification and detection of low radar-cross-section (RCS) targets. A new method of UWB radar signals generation with two-channel signal generator is presented. The realization structure is given; the principle and errors of signal synthesis are analyzed. At the same time, an automatic .adjustment measure of signal phase is proposed because of phase discontinuity of waveform in this method. The simulation experiment and analysis results indicate that radar signals with large instantaneous bandwidth can be generated by means of this method on the condition that the high-speed digital devices are limited.
文摘为了丰富紫花苜蓿转录组数据信息,找出不同品种紫花苜蓿的差异基因及代谢通路。通过Illumina HiSeq 4000平台对准格尔和WL319HQ的苜蓿叶片的RNA文库进行de novo组装。得到了约39G总的核苷酸,2亿多个reads,组装得到66734个Unigenes,平均长度为869 bp。将所得到的Unigenes与NCBI nonredundant protein(Nr),A manually annotated and reviewed protein sequence database(Swissprot),Clusters of eukaryotic orthologous groups(KOG)和Kyoto encyclopedia of genes and genomes(KEGG)数据库比对,分别获得44888(67.26%),29190(43.74%),24844(37.23%)和15647(23.45%)条序列的注释信息。在2个紫花苜蓿叶片中找到1098个差异表达基因(DEGs),其中有706个上调,392个下调(准格尔-vs-WL319HQ)。对其差异基因做了Gene ontology(GO)功能分析和KEGG途径分析,初步分析了2个品种营养品质差异的内在原因。极大地丰富了紫花苜蓿转录组数据信息,为今后紫花苜蓿的转录组测序提供理论依据,同时为紫花苜蓿生产实践提供参考。