Background: Large-sequencing cancer genome projects have shown that tumors have thousands of molecular alterations and their frequency is highly heterogeneous. In such scenarios, physicians and oncologists routinely face lists of cancer genomic alterations where only a minority of them are relevant biomarkers to drive clinical decision-making. For this reason, the medical community agrees on the urgent need of methodologies to establish the relevance of tumor alterations, assisting in genomic profile interpretation, and, more importantly, to prioritize those that could be clinically actionable for cancer therapy.Results: We present PanDrugs, a new computational methodology to guide the selection of personalized treatments in cancer patients...
Background: Human genome sequencing has enabled the association of phenotypes with genetic loci, but...
Over time, much has been done in attempt to understand the various causes and complex molecular mech...
Abstract Background Although large-scale, next-generation sequencing (NGS) studies of cancers hold p...
Abstract Background Large-sequencing cancer genome projects have shown that tumors have thousands of...
Genomics studies routinely confront researchers with long lists of tumor alterations detected in pat...
SummaryLarge efforts dedicated to detect somatic alterations across tumor genomes/exomes are expecte...
The complexity of human cancer underlies its devastating clinical consequences. Drugs designed to ta...
International audienceTargeted therapies have revolutionized the treatment of many cancers. Widely d...
Tesis doctoral inédita leída en la Universidad Autónoma de Madrid, Facultad de Medicina, Departament...
Large efforts dedicated to detect somatic alterations across tumor genomes/exomes are expected to pr...
INTRODUCTION: The focus of this study is the testing of biomarker-driven analytical methods to ident...
Background: Genomic alterations affecting drug target proteins occur in several tumor types and are ...
In silico drug prescription tools for precision cancer medicine can match molecular alterations with...
Cancer is a heterogeneous disease characterized by unregulated cell growth and promoted by mutations...
Identification of actionable genomic vulnerabilities is key to precision oncology. Utilizing a large...
Background: Human genome sequencing has enabled the association of phenotypes with genetic loci, but...
Over time, much has been done in attempt to understand the various causes and complex molecular mech...
Abstract Background Although large-scale, next-generation sequencing (NGS) studies of cancers hold p...
Abstract Background Large-sequencing cancer genome projects have shown that tumors have thousands of...
Genomics studies routinely confront researchers with long lists of tumor alterations detected in pat...
SummaryLarge efforts dedicated to detect somatic alterations across tumor genomes/exomes are expecte...
The complexity of human cancer underlies its devastating clinical consequences. Drugs designed to ta...
International audienceTargeted therapies have revolutionized the treatment of many cancers. Widely d...
Tesis doctoral inédita leída en la Universidad Autónoma de Madrid, Facultad de Medicina, Departament...
Large efforts dedicated to detect somatic alterations across tumor genomes/exomes are expected to pr...
INTRODUCTION: The focus of this study is the testing of biomarker-driven analytical methods to ident...
Background: Genomic alterations affecting drug target proteins occur in several tumor types and are ...
In silico drug prescription tools for precision cancer medicine can match molecular alterations with...
Cancer is a heterogeneous disease characterized by unregulated cell growth and promoted by mutations...
Identification of actionable genomic vulnerabilities is key to precision oncology. Utilizing a large...
Background: Human genome sequencing has enabled the association of phenotypes with genetic loci, but...
Over time, much has been done in attempt to understand the various causes and complex molecular mech...
Abstract Background Although large-scale, next-generation sequencing (NGS) studies of cancers hold p...