相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies
Yi Han et al.
NUCLEIC ACIDS RESEARCH (2019)
MEXPRESS update 2019
Alexander Koch et al.
NUCLEIC ACIDS RESEARCH (2019)
Leveraging European infrastructures to access 1 million human genomes by 2022
Gary Saunders et al.
NATURE REVIEWS GENETICS (2019)
ELMER v.2: an R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles
Tiago C. Silva et al.
BIOINFORMATICS (2019)
Co-expression of XIAP and CIAP1 Play Synergistic Effect on Patient's Prognosis in Head and Neck Cancer
Xi-Hu Yang et al.
PATHOLOGY & ONCOLOGY RESEARCH (2019)
The Network of Cancer Genes (NCG): a comprehensive catalogue of known and candidate cancer genes from cancer sequencing screens
Dimitra Repana et al.
GENOME BIOLOGY (2019)
Co-occurring genomic alterations in non-small-cell lung cancer biology and therapy
Ferdinandos Skoulidis et al.
NATURE REVIEWS CANCER (2019)
LinkedOmics: analyzing multi-omics data within and across 32 cancer types
Suhas V. Vasaikar et al.
NUCLEIC ACIDS RESEARCH (2018)
MethylMix 2.0: an R package for identifying DNA methylation genes
Pierre-Louis Cedoz et al.
BIOINFORMATICS (2018)
An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics
Jianfang Liu et al.
CELL (2018)
Oncogenic Signaling Pathways in The Cancer Genome Atlas
Francisco Sanchez-Vega et al.
CELL (2018)
The Cancer Omics Atlas: an integrative resource for cancer omics annotations
Qingrong Sun et al.
BMC MEDICAL GENOMICS (2018)
The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers
Zbyslaw Sondka et al.
NATURE REVIEWS CANCER (2018)
Development of a RNA-Seq Based Prognostic Signature in Lung Adenocarcinoma
Sudhanshu Shukla et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2017)
YM500v3: a database for small RNA sequencing in human cancer research
I-Fang Chung et al.
NUCLEIC ACIDS RESEARCH (2017)
Development of a RNA-Seq Based Prognostic Signature in Lung Adenocarcinoma
Sudhanshu Shukla et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2017)
GenomeVIP: a cloud platform for genomic variant discovery and interpretation
R. Jay Mashl et al.
GENOME RESEARCH (2017)
Integration of multiple OMIC biomarkers: A precision medicine strategy for lung cancer
Ana I. Robles et al.
LUNG CANCER (2017)
On the Interpretation of the Hazard Ratio and Communication of Survival Benefit
Andreas Sashegyi et al.
ONCOLOGIST (2017)
Conditional Selection of Genomic Alterations Dictates Cancer Evolution and Oncogenic Dependencies
Marco Mina et al.
CANCER CELL (2017)
Molecular Imaging and Precision Medicine in Lung Cancer
Katherine A. Zukotynski et al.
PET CLINICS (2017)
iGC-an integrated analysis package of gene expression and copy number alteration
Yi-Pin Lai et al.
BMC BIOINFORMATICS (2017)
TCGA2BED: extracting, extending, integrating, and querying The Cancer Genome Atlas
Fabio Cumbo et al.
BMC BIOINFORMATICS (2017)
DriverDBv2: a database for human cancer driver gene research
I-Fang Chung et al.
NUCLEIC ACIDS RESEARCH (2016)
TCGAbiolinks: an R/Bioconductor package for integrative analysis of TCGA data
Antonio Colaprico et al.
NUCLEIC ACIDS RESEARCH (2016)
SynTarget: an online tool to test the synergetic effect of genes on survival outcome in cancer
I. Amelio et al.
CELL DEATH AND DIFFERENTIATION (2016)
MethylMix: an R package for identifying DNA methylation-driven genes
Olivier Gevaert
BIOINFORMATICS (2015)
Pancancer analysis of DNA methylation-driven genes using MethylMix
Olivier Gevaert et al.
GENOME BIOLOGY (2015)
Systematic identification of cancer driving signaling pathways based on mutual exclusivity of genomic alterations
Ozgun Babur et al.
GENOME BIOLOGY (2015)
YM500v2: a small RNA sequencing (smRNA-seq) database for human cancer miRNome research
Wei-Chung Cheng et al.
NUCLEIC ACIDS RESEARCH (2015)
CoMEt: a statistical approach to identify combinations of mutually exclusive alterations in cancer
Mark D. M. Leiserson et al.
GENOME BIOLOGY (2015)
PROGgeneV2: enhancements on the existing database
Chirayu Pankaj Goswami et al.
BMC CANCER (2014)
Cross-Species Regulatory Network Analysis Identifies a Synergistic Interaction between FOXM1 and CENPF that Drives Prostate Cancer Malignancy
Alvaro Aytes et al.
CANCER CELL (2014)
DriverDB: an exome sequencing database for cancer driver gene identification
Wei-Chung Cheng et al.
NUCLEIC ACIDS RESEARCH (2014)
YM500: a small RNA sequencing (smRNA-seq) database for microRNA research
Wei-Chung Cheng et al.
NUCLEIC ACIDS RESEARCH (2013)
SurvExpress: An Online Biomarker Validation Tool and Database for Cancer Gene Expression Data Using Survival Analysis
Raul Aguirre-Gamboa et al.
PLOS ONE (2013)
Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal
Jianjiong Gao et al.
SCIENCE SIGNALING (2013)
Identification of ovarian cancer driver genes by using module network integration of multi-omics data
Olivier Gevaert et al.
INTERFACE FOCUS (2013)
The cBio Cancer Genomics Portal: An Open Platform for Exploring Multidimensional Cancer Genomics Data
Ethan Cerami et al.
CANCER DISCOVERY (2012)
PrognoScan: a new database for meta-analysis of the prognostic value of genes
Hideaki Mizuno et al.
BMC MEDICAL GENOMICS (2009)
High-level coexpression of JAG1 and NOTCH1 is observed in human breast cancer and is associated with poor overall survival
M Reedijk et al.
CANCER RESEARCH (2005)
Coexpression of the type 1 growth factor receptor family members HER-1, HER-2, and HER-3 has a synergistic negative prognostic effect on breast carcinoma survival
SM Wiseman et al.
CANCER (2005)
分享论文
