Variation interpretation predictors: principles, types, performance, and choice

A Niroula, M Vihinen - Human mutation, 2016 - Wiley Online Library
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 …

Prioritizing cancer genes based on an improved random walk method

PJ Wei, FX Wu, J Xia, Y Su, J Wang, CH Zheng - Frontiers in genetics, 2020 - frontiersin.org
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 …

MEXCOwalk: mutual exclusion and coverage based random walk to identify cancer modules

R Ahmed, I Baali, C Erten, E Hoxha, H Kazan - Bioinformatics, 2020 - academic.oup.com
Motivation Genomic analyses from large cancer cohorts have revealed the mutational
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 …

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 …

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 …

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 …

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 …

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 …

Personalized prediction of genes with tumor-causing somatic mutations based on multi-modal deep Boltzmann machine

Y Li, F Fauteux, J Zou, A Nantel, Y Pan - Neurocomputing, 2019 - Elsevier
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 …