HumCFS

Manually curated database of human chromosomal fragile sites. HumCFS provides useful information on fragile sites such as coordinates on the chromosome, cytoband, their chemical inducers and frequency of fragile site (rare or common), genes and miRNAs lying in fragile sites.

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HumCFS: a database of fragile sites in human chromosomes
PMID: 30999860

metasource: bio.tools
version: extracted_at: 2022-11-04T11:23:28.913830

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• HumCFS: a database of fragile sites in human chromosomes PubMed citations: 23.

  23 articles citing: HumCFS: a database of fragile sites in human chromosomes

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  Clustering and graph mining techniques for classification of complex structural variations in cancer genomes. PMID:35228601

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  The insertion and dysregulation of transposable elements in osteosarcoma and their association with patient event-free survival. PMID:35013466

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  AU-Rich Element RNA Binding Proteins: At the Crossroads of Post-Transcriptional Regulation and Genome Integrity. PMID:35008519

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  The epigenetic regulator LSH maintains fork protection and genomic stability via MacroH2A deposition and RAD51 filament formation. PMID:34112784

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  Confined placental mosaicism involving multiple de novo copy number variants associated with fetal growth restriction: A case report. PMID:33750025

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  An extended APOBEC3A mutation signature in cancer. PMID:33707442

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  Genomic Adaption and Mutational Patterns in a HaCaT Subline Resistant to Alkylating Agents and Ionizing Radiation. PMID:33498964

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  Tracking telomere fusions through crisis reveals conflict between DNA transcription and the DNA damage response. PMID:33447828

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  UV-exposure, endogenous DNA damage, and DNA replication errors shape the spectra of genome changes in human skin. PMID:33444353

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  RTEL1 Regulates G4/R-Loops to Avert Replication-Transcription Collisions. PMID:33357438

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  Genome-wide mutational signatures revealed distinct developmental paths for human B cell lymphomas. PMID:33136155

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  Systematic investigation of promoter substitutions resulting from somatic intrachromosomal structural alterations in diverse human cancers. PMID:33097743

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  Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs. PMID:33007263

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  Merkel Cell Polyomavirus in Merkel Cell Carcinoma: Integration Sites and Involvement of the KMT2D Tumor Suppressor Gene. PMID:32878339

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  Breast and prostate cancers harbor common somatic copy number alterations that consistently differ by race and are associated with survival. PMID:32819446

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  Small RNAs, Big Diseases. PMID:32784829

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  DNA Hypermethylation and Unstable Repeat Diseases: A Paradigm of Transcriptional Silencing to Decipher the Basis of Pathogenic Mechanisms. PMID:32580525

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  Genome-wide high-resolution mapping of mitotic DNA synthesis sites and common fragile sites by direct sequencing. PMID:32561861

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  RBMX is required for activation of ATR on repetitive DNAs to maintain genome stability. PMID:32494026

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  RTEL1 suppresses G-quadruplex-associated R-loops at difficult-to-replicate loci in the human genome. PMID:32398827

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  Comprehensive Molecular Characterization Identifies Distinct Genomic and Immune Hallmarks of Renal Medullary Carcinoma. PMID:32359397

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  VISDB: a manually curated database of viral integration sites in the human genome. PMID:31598702

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  APBioNet's annual International Conference on Bioinformatics (InCoB) returns to India in 2018. PMID:30999857

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functional, regulatory and non-coding rna

metasource: bio.tools
version: extracted_at: 2022-11-04T11:23:28.913830

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dna

metasource: bio.tools
version: extracted_at: 2022-11-04T11:23:28.913830

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pathology

metasource: bio.tools
version: extracted_at: 2022-11-04T11:23:28.913830

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functional, regulatory and non-coding rna dna pathology