Detection of Pathogenic Microbe Composition Using Next-Generation Sequencing Data

por Zhao, Haiyong, Wang, Shuang, Yuan, Xiguo
Publicado 2020

A Density Peak-Based Method to Detect Copy Number Variations From Next-Generation Sequencing Data

por Xie, Kun, Tian, Ye, Yuan, Xiguo
Publicado 2021

HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data

por Guo, Yang, Wang, Shuzhen, Yuan, Xiguo
Publicado 2021

A shortest path-based approach for copy number variation detection from next-generation sequencing data

por Liu, Guojun, Yang, Hongzhi, Yuan, Xiguo
Publicado 2023

DINTD: Detection and Inference of Tandem Duplications From Short Sequencing Reads

por Dong, Jinxin, Qi, Minyong, Wang, Shaoqiang, Yuan, Xiguo
Publicado 2020

RKDOSCNV: A Local Kernel Density-Based Approach to the Detection of Copy Number Variations by Using Next-Generation Sequencing Data

por Liu, Guojun, Zhang, Junying, Yuan, Xiguo, Wei, Chao
Publicado 2020

Integrating Somatic Mutations for Breast Cancer Survival Prediction Using Machine Learning Methods

por He, Zongzhen, Zhang, Junying, Yuan, Xiguo, Zhang, Yuanyuan
Publicado 2021

Comparative Analysis of Methods for Identifying Recurrent Copy Number Alterations in Cancer

por Yuan, Xiguo, Zhang, Junying, Zhang, Shengli, Yu, Guoqiang, Wang, Yue
Publicado 2012

FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm

por Tuo, Shouheng, Zhang, Junying, Yuan, Xiguo, Zhang, Yuanyuan, Liu, Zhaowen
Publicado 2016

Random Subspace Aggregation for Cancer Prediction with Gene Expression Profiles

por Yang, Liying, Liu, Zhimin, Yuan, Xiguo, Wei, Jianhua, Zhang, Junying
Publicado 2016

Analysis of breast cancer subtypes by AP-ISA biclustering

por Yang, Liying, Shen, Yunyan, Yuan, Xiguo, Zhang, Junying, Wei, Jianhua
Publicado 2017

Comparative study of whole exome sequencing-based copy number variation detection tools

por Zhao, Lanling, Liu, Han, Yuan, Xiguo, Gao, Kun, Duan, Junbo
Publicado 2020

Accurate Inference of Tumor Purity and Absolute Copy Numbers From High-Throughput Sequencing Data

por Yuan, Xiguo, Li, Zhe, Zhao, Haiyong, Bai, Jun, Zhang, Junying
Publicado 2020

MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data

por Zhao, Haiyong, Huang, Tihao, Li, Junqing, Liu, Guojun, Yuan, Xiguo
Publicado 2020

Niche harmony search algorithm for detecting complex disease associated high-order SNP combinations

por Tuo, Shouheng, Zhang, Junying, Yuan, Xiguo, He, Zongzhen, Liu, Yajun, Liu, Zhaowen
Publicado 2017

Author Correction: Niche harmony search algorithm for detecting complex disease associated high-order SNP combinations

por Tuo, Shouheng, Zhang, Junying, Yuan, Xiguo, He, Zongzhen, Liu, Yajun, Liu, Zhaowen
Publicado 2018

Stratification of Breast Cancer by Integrating Gene Expression Data and Clinical Variables

por He, Zongzhen, Zhang, Junying, Yuan, Xiguo, Xi, Jianing, Liu, Zhaowen, Zhang, Yuanyuan
Publicado 2019

Detection of False-Positive Deletions from the Database of Genomic Variants

por Duan, Junbo, Liu, Han, Zhao, Lanling, Yuan, Xiguo, Wang, Yu-Ping, Wan, Mingxi
Publicado 2019

TAGCNA: A Method to Identify Significant Consensus Events of Copy Number Alterations in Cancer

por Yuan, Xiguo, Zhang, Junying, Yang, Liying, Zhang, Shengli, Chen, Baodi, Geng, Yaojun, Wang, Yue
Publicado 2012

Network based stratification of major cancers by integrating somatic mutation and gene expression data

por He, Zongzhen, Zhang, Junying, Yuan, Xiguo, Liu, Zhaowen, Liu, Baobao, Tuo, Shouheng, Liu, Yajun
Publicado 2017