文献标题 | 分类 | 期刊 | IF |
Xenbase: deep integration of GEO & SRA RNA-seq and ChIP-seq data in a model organism database. | 数据库 | Nucleic Acids Res | 11.50 |
LncTarD: a manually-curated database of experimentally-supported functional lncRNA-target regulations in human diseases. | 数据库 | Nucleic Acids Res | 11.50 |
ChimerDB 4.0: an updated and expanded database of fusion genes. | 数据库 | Nucleic Acids Res | 11.50 |
LnCeVar: a comprehensive database of genomic variations that disturb ceRNA network regulation. | 数据库 | Nucleic Acids Res | 11.50 |
DNMIVD: DNA methylation interactive visualization database. | 数据库 | Nucleic Acids Res | 11.50 |
SNP2APA: a database for evaluating effects of genetic variants on alternative polyadenylation in human cancers. | 数据库 | Nucleic Acids Res | 11.50 |
ncRNA-eQTL: a database to systematically evaluate the effects of SNPs on non-coding RNA expression across cancer types. | 数据库 | Nucleic Acids Res | 11.50 |
TIMER2.0 for analysis of tumor-infiltrating immune cells. | 数据库 | Nucleic Acids Res | 11.50 |
CVCDAP: an integrated platform for molecular and clinical analysis of cancer virtual cohorts. | 数据库 | Nucleic Acids Res | 11.50 |
miRactDB characterizes miRNA-gene relation switch between normal and cancer tissues across pan-cancer. | 数据库 | Brief Bioinform | 8.99 |
Network control principles for identifying personalized driver genes in cancer. | 生信 方法 | Brief Bioinform | 8.99 |
TOD-CUP: a gene expression rank-based majority vote algorithm for tissue origin diagnosis of cancers of unknown primary. | 生信 方法 | Brief Bioinform
| 8.99 |
DiSNEP: a Disease-Specific gene Network Enhancement to improve Prioritizing candidate disease genes. | 生信 方法 | Brief Bioinform | 8.99 |
DeepHPV: a deep learning model to predict human papillomavirus integration sites. | 生信 方法 | Brief Bioinform | 8.99 |
Extended application of genomic selection to screen multiomics data for prognostic signatures of prostate cancer. | 生信 方法 | Brief Bioinform | 8.99 |
Highly accurate diagnosis of papillary thyroid carcinomas based on personalized pathways coupled with machine learning. | 生信 方法 | Brief Bioinform | 8.99 |
CNApp, a tool for the quantification of copy number alterations and integrative analysis revealing clinical implications. | 生信 方法 | Elife | 7.08 |
sTAM: An Online Tool for the Discovery of miRNA-Set Level Disease Biomarkers. | 生信 方法 | Mol Ther Nucleic Acids | 7.03 |
Reference-free deconvolution, visualization and interpretation of complex DNA methylation data using DecompPipeline, MeDeCom and FactorViz. | 生信 方法 | Nat Protoc | 10.41 |
A reference profile-free deconvolution method to infer cancer cell-intrinsic subtypes and tumor-type-specific stromal profiles. | 生信 方法 | Genome Med | 10.67 |
Characterization of the dual functional effects of heat shock proteins (HSPs) in cancer hallmarks to aid development of HSP inhibitors. | 生信 方法 | Genome Med | 10.67 |
CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data. | 生信 方法 | Genome Biol | 10.80 |
Weakly Supervised Deep Learning for Whole Slide Lung Cancer Image Analysis. | 生信 方法 | IEEE Trans Cybern | 11.07 |
Image-based consensus molecular subtype (imCMS) classification of colorectal cancer using deep learning. | 生信 方法 | Gut | 19.81 |