culinary 发表于 2025-3-21 18:17:27
书目名称Non-coding RNAs in Complex Diseases影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0667076<br><br> <br><br>书目名称Non-coding RNAs in Complex Diseases读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0667076<br><br> <br><br>NOVA 发表于 2025-3-21 20:26:39
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Book 2018. It conveys state-of-the-art bioinformatics tools and methods for ncRNAs from computational detection, functional prediction, to their roles in diseases. Computational methods used to investigate uncharacterised ncRNAs in diseases are mainly summarized in seven aspects: DNA variation of ncRNAs in dAccomplish 发表于 2025-3-22 15:49:59
Systematic Identification of Non-coding RNAs, to re-annotate lncRNAs from microarray data. We summarized multiple resources and databases for lncRNA annotation and compared their annotation processes and specific parameters. Finally, we utilized RNA-seq and miRNA-seq data to construct a comprehensive transcriptome containing miRNAs, lncRNAs and protein-coding genes in heart failure.万花筒 发表于 2025-3-22 21:04:30
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Aberrant Epigenetic Modifications of Non-coding RNAs in Human Disease,for PRC2-binding genes. At last, we inferred some lncRNAs with aberrant epigenetic modifications in glioblastoma and Alzheimer’s disease, and proved that theses lncRNAs may contribute to the initiation of human diseases.Catheter 发表于 2025-3-23 01:51:18
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Computational Inferring of Risk Subpathways Mediated by Dysfunctional Non-coding RNAs,nd pathway topologies. By applying methods to several disease datasets, we confirmed that our methods is effective in identifying risk subpathways and also can help uncover key non-coding RNAs in diseases. Additionally, reproducibility and robustness analysis demonstrated our methods are reliable.