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BMC Medical Genomics|June 26, 2023
Intronic position +9 and -9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing dataLi Zhang, Minna Shen, Xianhong Shu, et al.
BMC Medical Genomics|November 6, 2019
Correction to: Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traitsBenjamin S Glicksberg, Letizia Amadori, Nicholas K Akers, et al.
BMC Medical Genomics|January 30, 2019
Identification of sequence variants associated with severe microtia-astresia by targeted sequencingPu Wang, Yibei Wang, Xinmiao Fan, et al.
BMC Medical Genomics|February 2, 2019
Integration of genomic copy number variations and chemotherapy-response biomarkers in pediatric sarcomaLijun Cheng, Pankita H Pandya, Enze Liu, et al.
BMC Medical Genomics|February 2, 2019
Detecting virus integration sites based on multiple related sequencing data by VirTectYuchao Xia, Yun Liu, Minghua Deng, et al.
BMC Medical Genomics|November 10, 2019
A functional polymorphism in the promoter of miR-17-92 cluster is associated with decreased risk of ischemic strokeHuatuo Huang, Guijiang Wei, Chunfang Wang, et al.
BMC Medical Genomics|November 10, 2019
Significant random signatures reveals new biomarker for breast cancerElnaz Saberi Ansar, Changiz Eslahchii, Mahsa Rahimi, et al.
BMC Medical Genomics|February 10, 2019
Transcriptomic and ChIP-sequence interrogation of EGFR signaling in HER2+ breast cancer cells reveals a dynamic chromatin landscape and S100 genes as targetsMiguel Nava, Pranabananda Dutta, Nathan R Zemke, et al.
BMC Medical Genomics|December 21, 2019
Finding prognostic gene pairs for cancer from patient-specific gene networksByungkyu Park, Wook Lee, Inhee Park, et al.
BMC Medical Genomics|December 21, 2019
Identification of lung cancer gene markers through kernel maximum mean discrepancy and information entropyZhixun Zhao, Hui Peng, Xiaocai Zhang, et al.
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