Genomic hallmarks and therapeutic targets of ribosome biogenesis in cancer.
Briefings Bioinform., January, 2024
KRAS status predicted by pretreatment MRI radiomics was associated with lung metastasis in locally advanced rectal cancer patients.
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BMC Medical Imaging, December, 2023
An updated overview of experimental and computational approaches to identify non-canonical DNA/RNA structures with emphasis on G-quadruplexes and R-loops.
Briefings Bioinform., November, 2022
Comprehensive evaluation of computational methods for predicting cancer driver genes.
Briefings Bioinform., 2022
OncoVar: an integrated database and analysis platform for oncogenic driver variants in cancers.
Nucleic Acids Res., 2021
A new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing.
Briefings Bioinform., 2021
OncoBase: a platform for decoding regulatory somatic mutations in human cancers.
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Nucleic Acids Res., 2019
EpiDenovo: a platform for linking regulatory de novo mutations to developmental epigenetics and diseases.
Nucleic Acids Res., 2018
VarCards: an integrated genetic and clinical database for coding variants in the human genome.
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Nucleic Acids Res., 2018
CirGRDB: a database for the genome-wide deciphering circadian genes and regulators.
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Nucleic Acids Res., 2018
RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins.
Nucleic Acids Res., 2016
MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation.
Nucleic Acids Res., 2010