genomic DNA drug

Aliases

DNA

External links

DrugBank · PubChem

Related entities (10)

Mentioned in (77)

Papers in which this entity is mentioned.

• Enhancer activation from transposable elements in extrachromosomal DNA. (2025)
• Rapid brain tumor classification from sparse epigenomic data. (2025)
• MYC ecDNA promotes intratumour heterogeneity and plasticity in PDAC. (2025)
• Benchmarking short and long read polishing tools for nanopore assemblies: achieving near-perfect genomes for outbreak isolates. (2024)
• GCparagon: evaluating and correcting GC biases in cell-free DNA at the fragment level. (2023)
• At the dawn: cell-free DNA fragmentomics and gene regulation. (2022)
• Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smoking. (2022)
• Single-cell genomic variation induced by mutational processes in cancer. (2022)
• Inferring gene expression from cell-free DNA fragmentation profiles. (2022)
• Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
• A Comprehensive Circulating Tumor DNA Assay for Detection of Translocation and Copy-Number Changes in Pediatric Sarcomas. (2021)
• Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
• Immuno-genomic landscape of osteosarcoma. (2020)
• Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring. (2020)
• Neonatal Alcohol Exposure in Mice Induces Select Differentiation- and Apoptosis-Related Chromatin Changes Both Independent of and Dependent on Sex. (2020)
• Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors. (2020)
• Genome-wide DNA methylation comparison between live human brain and peripheral tissues within individuals. (2019)
• Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish. (2019)
• Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells. (2018)
• Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing. (2018)
• Positively selected enhancer elements endow osteosarcoma cells with metastatic competence. (2018)
• Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
• Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
• Nanopore Sequencing Reveals High-Resolution Structural Variation in the Cancer Genome (2017)
• A pooled mutational analysis identifies ionizing radiation-associated mutational signatures conserved between mouse and human malignancies. (2017)
• Orthotopic patient-derived xenografts of paediatric solid tumours. (2017)
• Mapping and phasing of structural variation in patient genomes using nanopore sequencing. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• DNA Methylation Analysis: Choosing the Right Method. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• Alteration of Gene Expression, DNA Methylation, and Histone Methylation in Free Radical Scavenging Networks in Adult Mouse Hippocampus following Fetal Alcohol Exposure. (2016)
• Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer. (2016)
• Development and clinical application of an integrative genomic approach to personalized cancer therapy. (2016)
• Dose-dependent alcohol-induced alterations in chromatin structure persist beyond the window of exposure and correlate with fetal alcohol syndrome birth defects. (2015)
• A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis. (2015)
• Clinical exome performance for reporting secondary genetic findings. (2015)
• CONSERTING: integrating copy-number analysis with structural-variation detection. (2015)
• Comprehensive genomic profiles of small cell lung cancer. (2015)
• Condensins are Required for Maintenance of Nuclear Architecture. (2014)
• Detecting ultralow-frequency mutations by Duplex Sequencing. (2014)
• Gene expression signatures affected by alcohol-induced DNA methylomic deregulation in human embryonic stem cells. (2014)
• DNA methylation signatures link prenatal famine exposure to growth and metabolism. (2014)
• Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. (2014)
• An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. (2014)
• Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways. (2014)
• ACMG clinical laboratory standards for next-generation sequencing. (2013)
• Charting a dynamic DNA methylation landscape of the human genome. (2013)
• Characterizing and measuring bias in sequence data. (2013)
• Delta and kappa opioid receptor polymorphisms influence the effects of naltrexone on subjective responses to alcohol. (2012)
• Population-specificity of human DNA methylation. (2012)
• Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
• High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
• In vivo genome editing using a high-efficiency TALEN system. (2012)
• Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylation. (2012)
• Choline supplementation and DNA methylation in the hippocampus and prefrontal cortex of rats exposed to alcohol during development. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• A promoter polymorphism in the Per3 gene is associated with alcohol and stress response. (2012)
• HLA typing from RNA-Seq sequence reads. (2012)
• High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
• Alcohol alters DNA methylation patterns and inhibits neural stem cell differentiation. (2011)
• Extensive epigenetic reprogramming in human somatic tissues between fetus and adult. (2011)
• Postmortem interval effect on RNA and gene expression in human brain tissue. (2011)
• Effects of ethanol and NAP on cerebellar expression of the neural cell adhesion molecule L1. (2011)
• The serotonin transporter gene and startle response during nicotine deprivation. (2011)
• Temporally- and spatially-regulated transcriptional activity of the nicotinic acetylcholine receptor beta4 subunit gene promoter. (2010)
• DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
• Association study of 182 candidate genes in anorexia nervosa. (2010)
• Fine mapping of calcineurin (PPP3CA) gene reveals novel alternative splicing patterns, association of 5'UTR trinucleotide repeat with addiction vulnerability, and differential isoform expression in Alzheimer's disease. (2010)
• Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition. (2010)
• MIQE précis: Practical implementation of minimum standard guidelines for fluorescence-based quantitative real-time PCR experiments. (2010)
• Variants in nicotinic acetylcholine receptors alpha5 and alpha3 increase risks to nicotine dependence. (2009)
• A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
• High-resolution mapping of copy-number alterations with massively parallel sequencing. (2009)
• Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample. (2009)
• Effects of ethanol and ipsapirone on the expression of genes encoding anti-apoptotic proteins and an antioxidant enzyme in ethanol-treated neurons. (2009)
• Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
• Rapid SNP discovery and genetic mapping using sequenced RAD markers. (2008)

Merged raw entities (1)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.