Titlebook: Bioinformatics Research and Applications; 16th International S Zhipeng Cai,Ion Mandoiu,Xuan Guo Conference proceedings 2020 Springer Nature

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书目名称Bioinformatics Research and Applications影响因子(影响力)




书目名称Bioinformatics Research and Applications影响因子(影响力)学科排名




书目名称Bioinformatics Research and Applications网络公开度




书目名称Bioinformatics Research and Applications网络公开度学科排名




书目名称Bioinformatics Research and Applications被引频次




书目名称Bioinformatics Research and Applications被引频次学科排名




书目名称Bioinformatics Research and Applications年度引用




书目名称Bioinformatics Research and Applications年度引用学科排名




书目名称Bioinformatics Research and Applications读者反馈




书目名称Bioinformatics Research and Applications读者反馈学科排名

Derogate

https://doi.org/10.1007/978-3-322-93111-5ion term to dispatch gene-disease associations to individual isoforms, and reversely aggregate these dispatched associations to affiliated genes. Next, it fuses different genomics and transcriptomics data to replenish gene-disease associations and to induce a linear classifier for predicting isoform

concert

Funktionen und ihre Ableitungen,a and reduce the chance of filtering out potential candidates overlooked by a single clustering. In the search stage, EpIntMC applies Entropy score to screen SNPs in each cluster, and uses Jaccard similarity to merge the most similar clusters into candidate sets. After that, EpIntMC uses exhaustive

surrogate

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连系

Konventionen und Begriffe zu diesem Buch,oth naturally occurring human variants and somatic mutations in cancer. In the context of cancer, ~3 M somatic mutations were extracted from over 10,000 cancerous human samples. Of the entire human proteome, 593 protein-coding genes show statistically significant bias towards harmful mutations. Thes

Emg827

Konventionen und Begriffe zu diesem Buch,e classic structural variants that can be detected by state-of-the-art methods (e.g., SVIM and Sniffles), our experiments demonstrate recall improvements of up-to . without harming the precisions (i.e., above .). We also point out three directions to further improve structural variant detection in t

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