Variation interpretation predictors: principles, types, performance, and choice
Next‐generation sequencing methods have revolutionized the speed of generating variation
information. Sequence data have a plethora of applications and will increasingly be used for …
information. Sequence data have a plethora of applications and will increasingly be used for …
Prioritizing cancer genes based on an improved random walk method
Identifying driver genes that contribute to cancer progression from numerous passenger
genes, although a central goal, is a major challenge. The protein–protein interaction network …
genes, although a central goal, is a major challenge. The protein–protein interaction network …
MEXCOwalk: mutual exclusion and coverage based random walk to identify cancer modules
Motivation Genomic analyses from large cancer cohorts have revealed the mutational
heterogeneity problem which hinders the identification of driver genes based only on …
heterogeneity problem which hinders the identification of driver genes based only on …
Identification of gene expression pattern related to breast cancer survival using integrated TCGA datasets and genomic tools
Z Huang, H Duan, H Li - BioMed research international, 2015 - Wiley Online Library
Several large‐scale human cancer genomics projects such as TCGA offered huge genomic
and clinical data for researchers to obtain meaningful genomics alterations which intervene …
and clinical data for researchers to obtain meaningful genomics alterations which intervene …
Personalized cancer therapy prioritization based on driver alteration co-occurrence patterns
L Mateo, M Duran-Frigola, A Gris-Oliver, M Palafox… - Genome Medicine, 2020 - Springer
Identification of actionable genomic vulnerabilities is key to precision oncology. Utilizing a
large-scale drug screening in patient-derived xenografts, we uncover driver gene alteration …
large-scale drug screening in patient-derived xenografts, we uncover driver gene alteration …
Identifying modules of cooperating cancer drivers
MI Klein, VL Cannataro, JP Townsend… - Molecular systems …, 2021 - embopress.org
Identifying cooperating modules of driver alterations can provide insights into cancer
etiology and advance the development of effective personalized treatments. We present …
etiology and advance the development of effective personalized treatments. We present …
Integrating protein–protein interaction networks and somatic mutation data to detect driver modules in pan-cancer
H Wu, Z Chen, Y Wu, H Zhang, Q Liu - … Sciences: Computational Life …, 2021 - Springer
With the constant update of large-scale sequencing data and the continuous improvement of
cancer genomics data, such as International Cancer Genome Consortium (ICGC) and The …
cancer genomics data, such as International Cancer Genome Consortium (ICGC) and The …
Integrating gene mutation spectra from tumors and the general population with gene expression topological networks to identify novel cancer driver genes
D He, L Li, Z Lu, S Li, T Lan, F Liu, H Zhang, B Lei… - BioRxiv, 2023 - biorxiv.org
Background Understanding the genetics underlying cancer development and progression is
the most important goal of biomedical research to improve patient survival rates. Recently …
the most important goal of biomedical research to improve patient survival rates. Recently …
An integrated framework for identifying mutated driver pathway and cancer progression
W Zhang, SL Wang - IEEE/ACM transactions on computational …, 2017 - ieeexplore.ieee.org
Next-generation sequencing (NGS) technologies provide amount of somatic mutation data
in a large number of patients. The identification of mutated driver pathway and cancer …
in a large number of patients. The identification of mutated driver pathway and cancer …
Personalized prediction of genes with tumor-causing somatic mutations based on multi-modal deep Boltzmann machine
When diagnosed at an advanced stage, most cancer patients suffer from treatment failure,
recurrences and low survival. Taking advantage of high-throughput sequencing and deep …
recurrences and low survival. Taking advantage of high-throughput sequencing and deep …