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Frontiers in Genetics|October 26, 2020
PacBio Long Reads Improve Metagenomic Assemblies, Gene Catalogs, and Genome BinningHaiying Xie, Caiyun Yang, Yamin Sun, et al.
Frontiers in Genetics|October 26, 2020
Identification of a Twelve-Gene Signature and Establishment of a Prognostic Nomogram Predicting Overall Survival for MedulloblastomaSihan Zhu, Fuhua Lin, Zhenghe Chen, et al.
Frontiers in Genetics|October 26, 2020
Genome- and Transcriptome-Wide Identification of C3Hs in Common Bean (Phaseolus vulgaris L.) and Structural and Expression-Based Analyses of Their Functions During the Sprout Stage Under Salt-Stress ConditionsQi Zhang, Wen-Jing Zhang, Zhen-Gong Yin, et al.
Frontiers in Genetics|October 26, 2020
Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in IndiaAnshika Srivastava, Audditiya Bandopadhyay, Debashurti Das, et al.
Frontiers in Genetics|October 26, 2020
Characteristics of Organellar Genomes and Nuclear Internal Transcribed Spacers in the Tertiary Relict Genus Dipelta and Their Phylogenomic ImplicationsFangfang Peng, Zhe Zhao, Bei Xu, et al.
Frontiers in Genetics|April 2, 2020
Linkage Disequilibrium, Effective Population Size and Genomic Inbreeding Rates in American Mink Using Genotyping-by-Sequencing DataKarim Karimi, A Hossain Farid, Mehdi Sargolzaei, et al.
Frontiers in Genetics|March 21, 2020
Quantification of the Underlying Mechanisms and Relationships Among Cancer, Metastasis, and Differentiation and DevelopmentChong Yu, Qiong Liu, Cong Chen, et al.
Frontiers in Genetics|March 21, 2020
Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing EducationBelinda J McClaren, Emily A King, Erin Crellin, et al.
Frontiers in Genetics|March 21, 2020
Reconstruction and Validation of a Genome-Scale Metabolic Model of Streptococcus oralis (iCJ415), a Human Commensal and Opportunistic PathogenChristian S Jensen, Charles J Norsigian, Xin Fang, et al.
Frontiers in Genetics|March 21, 2020
Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric PatientsWei-Xing Feng, Xin-Ying Yang, Jiu-Wei Li, et al.
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