Author of the publication

An updated overview of experimental and computational approaches to identify non-canonical DNA/RNA structures with emphasis on G-quadruplexes and R-loops.

, , and . Briefings Bioinform., (November 2022)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

 

Other publications of authors with the same name

MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation., , , , , , , , and . Nucleic Acids Res., 38 (Web-Server-Issue): 732-736 (2010)OncoVar: an integrated database and analysis platform for oncogenic driver variants in cancers., , , , , , , , , and . Nucleic Acids Res., 49 (Database-Issue): D1289-D1301 (2021)An updated overview of experimental and computational approaches to identify non-canonical DNA/RNA structures with emphasis on G-quadruplexes and R-loops., , and . Briefings Bioinform., (November 2022)KRAS status predicted by pretreatment MRI radiomics was associated with lung metastasis in locally advanced rectal cancer patients., , , , , , , , , and 6 other author(s). BMC Medical Imaging, 23 (1): 210 (December 2023)Comprehensive evaluation of computational methods for predicting cancer driver genes., , , , , , and . Briefings Bioinform., (2022)Genomic hallmarks and therapeutic targets of ribosome biogenesis in cancer., , , , , , , and . Briefings Bioinform., (January 2024)OncoBase: a platform for decoding regulatory somatic mutations in human cancers., , , , , , , , , and 3 other author(s). Nucleic Acids Res., 47 (Database-Issue): D1044-D1055 (2019)RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins., , , , , , and . Nucleic Acids Res., 44 (Database-Issue): 154-163 (2016)VarCards: an integrated genetic and clinical database for coding variants in the human genome., , , , , , , , , and 1 other author(s). Nucleic Acids Res., 46 (Database-Issue): D1039-D1048 (2018)A new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing., , , , , , , , and . Briefings Bioinform., (2021)