Aiming at solving the blind estimation problem of dispreading spectrum sequence under low SNR, a spread-spectrum estimation algorithm based subspace tracking is studied in this paper. This method avoids the direct eig...Aiming at solving the blind estimation problem of dispreading spectrum sequence under low SNR, a spread-spectrum estimation algorithm based subspace tracking is studied in this paper. This method avoids the direct eigen decomposition, using the sliding window technique to obtain the code synchronization, then use segmentation subspace tracking method estimate spreading sequence and splice in a certain order to achieve pseudo-code blind estimation. The results show that the algorithm can complete the accurate estimation of PN code sequence in low SNR conditions, reduce the amount of data storage and be easy hardware implementation展开更多
Long PN-code acquisition is a difficult and time-consuming task due to long code period.To accelerate acquisition,folding methods like XFAST are widely used.In highdynamic environment however,the application of those ...Long PN-code acquisition is a difficult and time-consuming task due to long code period.To accelerate acquisition,folding methods like XFAST are widely used.In highdynamic environment however,the application of those methods are largely restricted due to nonnegligible residual frequency.This paper proposes a new dual-channel method for fast acquisition of long PN-code.In the proposed method,both non-overlapping local PNcode blocks are employed to correlate with input sample block;the detection process is eased through finding the maximum value among correlation results and verification is made with all the full and partial peaks taken into account.False alarm probabilities from analysis of the verification process are derived.Both theoretical and Monte Carlo simulations reveal that,with respect to acquisition probability and mean acquisition time under the same false alarm rate,dual-channel method has advantage over zero-padding and XFAST based folding methods under certain false alarm probabilities.展开更多
In the article“Silencing of the long non-coding RNA LINC00265 triggers autophagy and apoptosis in lung cancer by reducing protein stability of SIN3A oncogene”(Oncology Research.2024,Vol.32,No.7,pp.1185–1195.doi:10....In the article“Silencing of the long non-coding RNA LINC00265 triggers autophagy and apoptosis in lung cancer by reducing protein stability of SIN3A oncogene”(Oncology Research.2024,Vol.32,No.7,pp.1185–1195.doi:10.32604/or.2023.030771,https://www.techscience.com/or/v32n7/57163),an inadvertent error occurred during the compilation of Fig.3H.This needed corrections to ensure the accuracy and integrity of the data presented.展开更多
Long non-coding RNAs(lncRNAs)are members of the non-protein coding RNA family longer than 200 nucleotides.They participate in the regulation of gene and protein expression influencing apoptosis,cell proliferation and ...Long non-coding RNAs(lncRNAs)are members of the non-protein coding RNA family longer than 200 nucleotides.They participate in the regulation of gene and protein expression influencing apoptosis,cell proliferation and immune responses,thereby playing a critical role in the development and progression of various cancers,including colorectal cancer(CRC).As CRC is one of the most frequently diagnosed malignancies worldwide with high mortality,its screening and early detection are crucial,so the identification of disease-specific biomarkers is necessary.LncRNAs are promising candidates as they are involved in carcinogenesis,and certain lncRNAs(e.g.,CCAT1,CRNDE,CRCAL1-4)show altered expression in adenomas,making them potential early diagnostic markers.In addition to being useful as tissue-specific markers,analysis of circulating lncRNAs(e.g.,CCAT1,CCAT2,BLACAT1,CRNDE,NEAT1,UCA1)in peripheral blood offers the possibility to establish minimally invasive,liquid biopsy-based diagnostic tests.This review article aims to describe the origin,structure,and functions of lncRNAs and to discuss their contribution to CRC development.Moreover,our purpose is to summarise lncRNAs showing altered expression levels during tumor formation in both colon tissue and plasma/serum samples and to demonstrate their clinical implications as diagnostic or prognostic biomarkers for CRC.展开更多
Gastric cancer(GC) is the fourth most common cancer and the third leading cause of cancer mortality worldwide. Micro RNAs(mi RNAs) and long non-coding RNAs(lnc RNAs) are the most popular non-coding RNAs in cancer rese...Gastric cancer(GC) is the fourth most common cancer and the third leading cause of cancer mortality worldwide. Micro RNAs(mi RNAs) and long non-coding RNAs(lnc RNAs) are the most popular non-coding RNAs in cancer research. To date,the roles of mi RNAs and lnc RNAs have been extensively studied in GC,suggesting that mi RNAs and lnc RNAs represent a vital component of tumor biology. Furthermore,circulating mi RNAs and lnc RNAs are found to be dysregulated in patients with GC compared with healthy individuals. Circulating mi RNAs and lnc RNAs may function as promising biomarkers to improve the early detection of GC. Multiple possibilities for mi RNA secretion have been elucidated,including active secretion by microvesicles,exosomes,apoptotic bodies,highdensity lipoproteins and protein complexes as well as passive leakage from cells. However,the mechanism underlying lnc RNA secretion and the functions of circulating mi RNAs and lnc RNAs have not been fully illuminated. Concurrently,to standardize results of global investigations of circulating mi RNAs and lnc RNAs biomarker studies,several recommendations for preanalytic considerations are put forward. In this review,we summarize the known circulating mi RNAs and lnc RNAs for GC diagnosis. The possible mechanism of mi RNA and lnc RNA secretion as well as methodologies for identification of circulating mi RNAs and lnc RNAs are also discussed. The topics covered here highlight new insights into GC diagnosis and screening.展开更多
In the seismic safety evaluation (SSE) for key projects, the probability-consistent spectrum (PCS), usually obtained from probabilistic seismic hazard analysis (PSHA), is not consistent with the design response spectr...In the seismic safety evaluation (SSE) for key projects, the probability-consistent spectrum (PCS), usually obtained from probabilistic seismic hazard analysis (PSHA), is not consistent with the design response spectrum given by Code for Seismic Design of Buildings (GB50011-2001). Sometimes, there may be a remarkable difference be-tween them. If the PCS is lower than the corresponding code design response spectrum (CDS), the seismic fortifi-cation criterion for the key projects would be lower than that for the general industry and civil buildings. In the paper, the relation between PCS and CDS is discussed by using the ideal simple potential seismic source. The re-sults show that in the most areas influenced mainly by the potential sources of the epicentral earthquakes and the regional earthquakes, PCS is generally lower than CDS in the long periods. We point out that the long-period re-sponse spectra of the code should be further studied and combined with the probability method of seismic zoning as much as possible. Because of the uncertainties in SSE, it should be prudent to use the long-period response spectra given by SSE for key projects when they are lower than CDS.展开更多
文摘Aiming at solving the blind estimation problem of dispreading spectrum sequence under low SNR, a spread-spectrum estimation algorithm based subspace tracking is studied in this paper. This method avoids the direct eigen decomposition, using the sliding window technique to obtain the code synchronization, then use segmentation subspace tracking method estimate spreading sequence and splice in a certain order to achieve pseudo-code blind estimation. The results show that the algorithm can complete the accurate estimation of PN code sequence in low SNR conditions, reduce the amount of data storage and be easy hardware implementation
文摘Long PN-code acquisition is a difficult and time-consuming task due to long code period.To accelerate acquisition,folding methods like XFAST are widely used.In highdynamic environment however,the application of those methods are largely restricted due to nonnegligible residual frequency.This paper proposes a new dual-channel method for fast acquisition of long PN-code.In the proposed method,both non-overlapping local PNcode blocks are employed to correlate with input sample block;the detection process is eased through finding the maximum value among correlation results and verification is made with all the full and partial peaks taken into account.False alarm probabilities from analysis of the verification process are derived.Both theoretical and Monte Carlo simulations reveal that,with respect to acquisition probability and mean acquisition time under the same false alarm rate,dual-channel method has advantage over zero-padding and XFAST based folding methods under certain false alarm probabilities.
文摘In the article“Silencing of the long non-coding RNA LINC00265 triggers autophagy and apoptosis in lung cancer by reducing protein stability of SIN3A oncogene”(Oncology Research.2024,Vol.32,No.7,pp.1185–1195.doi:10.32604/or.2023.030771,https://www.techscience.com/or/v32n7/57163),an inadvertent error occurred during the compilation of Fig.3H.This needed corrections to ensure the accuracy and integrity of the data presented.
文摘目的计算并预测13 562个GENCODE项目首期鉴定的人类长链非编码RNA在16个哺乳动物的直系同源基因,并建立数据库Long Man,为长链非编码RNA研究提供重要数据。方法使用RNAfold预测13 562个人类长链非编码RNA每个外显子的结构;使用Infernal对每个外显子进行基因组搜索,分析其在16个哺乳动物可能的同源外显子;分析每个人类长链非编码RNA是否有同源基因;分析同源长链非编码RNA中的转座子和剪切信号;构造数据库的搜索引擎和输出界面;实现数据库维护更新机制。结果 Long Man目前收录133 646个直系同源长链非编码RNA;提供序列、比对、转座子和种系特异性插缺(indel)等信息;提供多条件组合查询;提供显示与下载功能。结论 Long Man是首个大规模多种系同源长链非编码RNA数据库,对长链非编码RNA比较与功能研究具有重要价值。
基金Supported by the National Research,Development and Innovation Office,No.NVKP_16-1-2016-0004
文摘Long non-coding RNAs(lncRNAs)are members of the non-protein coding RNA family longer than 200 nucleotides.They participate in the regulation of gene and protein expression influencing apoptosis,cell proliferation and immune responses,thereby playing a critical role in the development and progression of various cancers,including colorectal cancer(CRC).As CRC is one of the most frequently diagnosed malignancies worldwide with high mortality,its screening and early detection are crucial,so the identification of disease-specific biomarkers is necessary.LncRNAs are promising candidates as they are involved in carcinogenesis,and certain lncRNAs(e.g.,CCAT1,CRNDE,CRCAL1-4)show altered expression in adenomas,making them potential early diagnostic markers.In addition to being useful as tissue-specific markers,analysis of circulating lncRNAs(e.g.,CCAT1,CCAT2,BLACAT1,CRNDE,NEAT1,UCA1)in peripheral blood offers the possibility to establish minimally invasive,liquid biopsy-based diagnostic tests.This review article aims to describe the origin,structure,and functions of lncRNAs and to discuss their contribution to CRC development.Moreover,our purpose is to summarise lncRNAs showing altered expression levels during tumor formation in both colon tissue and plasma/serum samples and to demonstrate their clinical implications as diagnostic or prognostic biomarkers for CRC.
文摘Gastric cancer(GC) is the fourth most common cancer and the third leading cause of cancer mortality worldwide. Micro RNAs(mi RNAs) and long non-coding RNAs(lnc RNAs) are the most popular non-coding RNAs in cancer research. To date,the roles of mi RNAs and lnc RNAs have been extensively studied in GC,suggesting that mi RNAs and lnc RNAs represent a vital component of tumor biology. Furthermore,circulating mi RNAs and lnc RNAs are found to be dysregulated in patients with GC compared with healthy individuals. Circulating mi RNAs and lnc RNAs may function as promising biomarkers to improve the early detection of GC. Multiple possibilities for mi RNA secretion have been elucidated,including active secretion by microvesicles,exosomes,apoptotic bodies,highdensity lipoproteins and protein complexes as well as passive leakage from cells. However,the mechanism underlying lnc RNA secretion and the functions of circulating mi RNAs and lnc RNAs have not been fully illuminated. Concurrently,to standardize results of global investigations of circulating mi RNAs and lnc RNAs biomarker studies,several recommendations for preanalytic considerations are put forward. In this review,we summarize the known circulating mi RNAs and lnc RNAs for GC diagnosis. The possible mechanism of mi RNA and lnc RNA secretion as well as methodologies for identification of circulating mi RNAs and lnc RNAs are also discussed. The topics covered here highlight new insights into GC diagnosis and screening.
基金Shanghai Science & Technology Development Foundation (022512065) and Shanghai Construction Technology Development Foundation (A0206101).
文摘In the seismic safety evaluation (SSE) for key projects, the probability-consistent spectrum (PCS), usually obtained from probabilistic seismic hazard analysis (PSHA), is not consistent with the design response spectrum given by Code for Seismic Design of Buildings (GB50011-2001). Sometimes, there may be a remarkable difference be-tween them. If the PCS is lower than the corresponding code design response spectrum (CDS), the seismic fortifi-cation criterion for the key projects would be lower than that for the general industry and civil buildings. In the paper, the relation between PCS and CDS is discussed by using the ideal simple potential seismic source. The re-sults show that in the most areas influenced mainly by the potential sources of the epicentral earthquakes and the regional earthquakes, PCS is generally lower than CDS in the long periods. We point out that the long-period re-sponse spectra of the code should be further studied and combined with the probability method of seismic zoning as much as possible. Because of the uncertainties in SSE, it should be prudent to use the long-period response spectra given by SSE for key projects when they are lower than CDS.
