whole blood anatomy

Aliases

blood

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Mentioned in (21)

Papers in which this entity is mentioned.

• Integrative epigenetics and transcriptomics identify aging genes in human blood. (2026)
• Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
• Detection and characterization of lung cancer using cell-free DNA fragmentomes. (2021)
• Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
• Liquid versus tissue biopsy for detecting acquired resistance and tumor heterogeneity in gastrointestinal cancers. (2019)
• Hypermethylation of Proopiomelanocortin and Period 2 Genes in Blood Are Associated with Greater Subjective and Behavioral Motivation for Alcohol in Humans. (2019)
• RNA-Seq Signatures Normalized by mRNA Abundance Allow Absolute Deconvolution of Human Immune Cell Types. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• The impact of structural variation on human gene expression. (2017)
• 2D Representation of Transcriptomes by t-SNE Exposes Relatedness between Human Tissues. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• Systematic pan-cancer analysis of tumour purity. (2015)
• Robust enumeration of cell subsets from tissue expression profiles. (2015)
• Reconstructing A/B compartments as revealed by Hi-C using long-range correlations in epigenetic data. (2015)
• Maternal and neonatal plasma microRNA biomarkers for fetal alcohol exposure in an ovine model. (2014)
• Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
• Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)

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