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BMC Medical Genomics|July 5, 2022
Construction and validation of a prognostic risk model for breast cancer based on protein expressionBo Huang, Xujun Zhang, Qingyi Cao, et al.
BMC Medical Genomics|July 6, 2022
Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networksMinsu Kim, Jennifer E Huffman, Amy Justice, et al.
BMC Medical Genomics|December 9, 2022
Altered DNA methylation of CYP2E1 gene in schizophrenia patients with tardive dyskinesiaPing Zhang, Yanli Li, Kesheng Wang, et al.
BMC Medical Genomics|October 16, 2020
Accuracy and reproducibility of somatic point mutation calling in clinical-type targeted sequencing dataAli Karimnezhad, Gareth A Palidwor, Kednapa Thavorn, et al.
BMC Medical Genomics|October 7, 2020
A novel phenotype of 13q12.3 microdeletion characterized by epilepsy in an Asian child: a case reportMina Wang, Bin Li, Zehuan Liao, et al.
BMC Medical Genomics|October 22, 2020
Pan-cancer analysis of differential DNA methylation patternsMai Shi, Stephen Kwok-Wing Tsui, Hao Wu, et al.
BMC Medical Genomics|October 22, 2020
Improving lung cancer risk stratification leveraging whole transcriptome RNA sequencing and machine learning across multiple cohortsYoonha Choi, Jianghan Qu, Shuyang Wu, et al.
BMC Medical Genomics|February 1, 2020
Blood signatures for second stage human African trypanosomiasis: a transcriptomic approachJulius Mulindwa, Enock Matovu, John Enyaru, et al.
BMC Medical Genomics|March 5, 2020
4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case reportMaolan Wu, Xiangrong Zheng, Xia Wang, et al.
BMC Medical Genomics|August 29, 2020
A machine learning framework for genotyping the structural variations with copy number variantTian Zheng, Xiaoyan Zhu, Xuanping Zhang, et al.
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