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Frontiers in Genetics|October 17, 2022
Gene-specific machine learning model to predict the pathogenicity of BRCA2 variantsMohannad N Khandakji, Borbala MifsudFrontiers in Genetics|October 17, 2022
Identification of N6-methylandenosine related lncRNA signatures for predicting the prognosis and therapy response in colorectal cancer patientsZhiyong Li, Yang Liu, Huijie Yi, et al.Frontiers in Genetics|October 17, 2022
Critical role of guanylate binding protein 5 in tumor immune microenvironment and predictive value of immunotherapy responseXiang Li, Dan Song, Song Su, et al.Frontiers in Genetics|October 17, 2022
HRD-MILN: Accurately estimate tumor homologous recombination deficiency status from targeted panel sequencing dataXuwen Wang, Ying Xu, Yinbin Zhang, et al.Frontiers in Genetics|October 17, 2022
Drug repositioning for esophageal squamous cell carcinomaAdam N Bennett, Rui Xuan Huang, Qian He, et al.Frontiers in Genetics|October 17, 2022
Two subtypes of cutaneous melanoma with distinct mutational signatures and clinico-genomic characteristicsYoon-Seob Kim, Minho Lee, Yeun-Jun ChungFrontiers in Genetics|October 17, 2022
Development of a clinically validated in vitro functional assay to assess pathogenicity of novel GAA variants in patients with Pompe disease identified via newborn screeningShelly Goomber, Erin Huggins, Catherine W Rehder, et al.Frontiers in Genetics|October 17, 2022
Genome-wide identification and expression analysis of glutathione S-transferase gene family to reveal their role in cold stress response in cucumberXiaoyu Duan, Xuejing Yu, Yidan Wang, et al.Frontiers in Genetics|October 17, 2022
DETexT: An SNV detection enhancement for low read depth by integrating mutational signatures into TextCNNTian ZhengFrontiers in Genetics|October 17, 2022
Computational approaches for predicting variant impact: An overview from resources, principles to applicationsYe Liu, William S B Yeung, Philip C N Chiu, et al.Pageof 1,604