blood drug

Aliases

blood sample, blood tissue

External links

DrugBank · PubChem

Related entities (2)

Mentioned in (43)

Papers in which this entity is mentioned.

• Whole genome sequencing approach to assess homologous recombination deficiency in a pan-cancer cohort. (2026)
• Nanopore-based cell-free DNA fragmentation and methylation profiles from the cerebral spinal fluid of patients with lung cancer brain metastases. (2025)
• Stratified Medicine Pediatrics: Cell-Free DNA and Serial Tumor Sequencing Identifies Subtype-Specific Cancer Evolution and Epigenetic States. (2025)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
• Machine learning approaches to the identification of children affected by prenatal alcohol exposure: A narrative review. (2024)
• A DNA methylation atlas of normal human cell types. (2023)
• Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. (2023)
• Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
• mutations, genetic mosaicism and human disease. (2022)
• At the dawn: cell-free DNA fragmentomics and gene regulation. (2022)
• Circulating Tumor DNA as a Biomarker in Patients With Stage III and IV Wilms Tumor: Analysis From a Children's Oncology Group Trial, AREN0533. (2022)
• Application of third-generation sequencing in cancer research. (2021)
• Best practices for variant calling in clinical sequencing. (2020)
• Immune network dysregulation associated with child neurodevelopmental delay: modulatory role of prenatal alcohol exposure. (2020)
• Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring. (2020)
• Pan-cancer analysis of whole genomes. (2020)
• Serial liquid biopsies for detection of treatment failure and profiling of resistance mechanisms in -rearranged lung cancer. (2019)
• Genome-wide cell-free DNA fragmentation in patients with cancer. (2019)
• RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
• Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• Circular DNA elements of chromosomal origin are common in healthy human somatic tissue. (2018)
• The Immune Landscape of Cancer. (2018)
• Detection of circulating tumour DNA is associated with inferior outcomes in Ewing sarcoma and osteosarcoma: a report from the Children's Oncology Group. (2018)
• Tumor fraction in cell-free DNA as a biomarker in prostate cancer. (2018)
• Annotation-free quantification of RNA splicing using LeafCutter. (2018)
• Copy number signatures and mutational processes in ovarian carcinoma. (2018)
• Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
• Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors. (2017)
• Puberty and structural brain development in humans. (2017)
• An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
• Maternal choline supplementation in a sheep model of first trimester binge alcohol fails to protect against brain volume reductions in peripubertal lambs. (2016)
• Integrated digital error suppression for improved detection of circulating tumor DNA. (2016)
• The Ontology for Biomedical Investigations. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets. (2015)
• ACMG clinical laboratory standards for next-generation sequencing. (2013)
• Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
• Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
• Diffusion tensor imaging of the cerebellum and eyeblink conditioning in fetal alcohol spectrum disorder. (2011)
• TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays. (2010)
• Chronic binge ethanol-mediated acidemia reduces availability of glutamine and related amino acids in maternal plasma of pregnant sheep. (2008)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)

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