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Cancer
Pages starting with "Cancer"
Cancer stem cell
The cancer genome
Cancer-specific defects in DNA repair pathways as targets for personalized therapeutic approaches
Cancer panel
Cancer genomics
Cancer immunotherapy
The Cancer Genome Atlas
Cancer genomics: from discovery science to personalized medicine
Cancer genome data analysis and knowledgebase
Cancer epigenetics
Cancer Genomics Hub
Cancer Target Gene Screening: a web application for breast cancer target gene screening using multi-omics data analysis
Pages ending with "Cancer"
Lung cancer
Hepatic cancer
Colon cancer
JARID1B is a luminal lineage-driving oncogene in breast cancer
CDK12 Inhibition Reverses De Novo and Acquired PARP Inhibitor Resistance in BRCA Wild-Type and Mutated Models of Triple-Negative Breast Cancer
Meta-analysis of the global gene expression profile of triple-negative breast cancer identifies genes for the prognostication and treatment of aggressive breast cancer
Prognostic value of PDL1 expression in pancreatic cancer
An integrative approach to reveal driver gene fusions from paired-end sequencing data in cancer
Pancreatic cancer
Prostate cancer
Colorectal cancer
Genetic alterations of histone lysine methyltransferases and their significance in breast cancer
Ovarian cancer
Triple-negative breast cancer
Stomach cancer
Liver cancer
Genomics of Drug Sensitivity in Cancer
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer
Brain cancer
Microsatellite instability in colorectal cancer
Hereditary nonpolyposis colorectal cancer
Role of RBP2-Induced ER and IGF1R-ErbB Signaling in Tamoxifen Resistance in Breast Cancer
Thyroid cancer
Breast cancer
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Somatic evolution in cancer
Pages containing "Cancer"
Genetic alterations of triple negative breast cancer by targeted next-generation sequencing and correlation with tumor morphology
Sequence analysis of mutations and translocations across breast cancer subtypes
Identification of Biomarkers for Breast Cancer Using Databases
Identification of druggable cancer driver genes amplified across TCGA datasets
Triple-negative breast cancer: an unmet medical need
The life history of 21 breast cancers
MEDICI: Mining Essentiality Data to Identify Critical Interactions for Cancer Drug Target Discovery and Development
Biomarkers in triple negative breast cancer: A review
A mutational signature in gastric cancer suggests therapeutic strategies
Landscape of somatic mutations in 560 breast cancer whole-genome sequences
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine
The landscape of somatic copy-number alteration across human cancers
Breast cancer epigenetics: from DNA methylation to microRNAs
Complex landscapes of somatic rearrangement in human breast cancer genomes
Smyd3 Is a Transcriptional Potentiator of Multiple Cancer-Promoting Genes and Required for Liver and Colon Cancer Development
Predicting cancer-specific vulnerability via data-driven detection of synthetic lethality
Oncotator: cancer variant annotation tool
Mutational processes molding the genomes of 21 breast cancers
An integrative somatic mutation analysis to identify pathways linked with survival outcomes across 19 cancer types
International Cancer Genome Consortium
Pathway and network analysis of cancer genomes
Drug Discovery in Cancer Epigenetics
Patterns of somatic mutation in human cancer genomes
Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data
DOT1L cooperates with the c-Myc-p300 complex to epigenetically derepress CDH1 transcription factors in breast cancer progression
My Cancer Genome
Characterizing genomic alterations in cancer by complementary functional associations
BCL11A is a triple-negative breast cancer gene with critical functions in stem and progenitor cells
Comprehensive functional analysis of the tousled-like kinase 2 frequently amplified in aggressive luminal breast cancers
Next-Generation Sequencing of Circulating Tumor DNA for Early Cancer Detection
Global transcription network incorporating distal regulator binding reveals selective cooperation of cancer drivers and risk genes
Is the future of personalized therapy in triple-negative breast cancer based on molecular subtype
Tumor suppressor SET9 guides the epigenetic plasticity of breast cancer cells and serves as an early-stage biomarker for predicting metastasis
The topography of mutational processes in breast cancer genomes
Next generation sequencing of triple negative breast cancer to find predictors for chemotherapy response
Mechanisms underlying mutational signatures in human cancers
A framework for organizing cancer-related variations from existing databases, publications and NGS data using a High-performance Integrated Virtual Environment (HIVE)
Computational methods for detecting copy number variations in cancer genome using next generation sequencing
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