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Search 3,717 documents across 34 fields — every claim tier-rated by evidence
90 results for "genomic imprinting" — page 1 of 5
L_3_16 — Genomic Imprinting & Evolutionary Conflict
Genomic imprinting — the epigenetic phenomenon in which a subset of genes (~100–200 in mammals) are expressed from only one parental allele, with the other allele silenced by DNA methylation and histone modification esta
Z_1_05 — Genomic Imprinting and Parent-of-Origin Effects
Genomic imprinting is an epigenetic phenomenon in which a gene's expression depends on whether it was inherited from the mother or the father — violating the standard Mendelian assumption that both parental copies functi
Z_3_16 — Genomic Conflict and Selfish Genetic Elements
Selfish genetic elements (SGEs) — sequences of DNA that promote their own transmission at the expense of the host organism or other genes in the genome — reveal that the genome is not a cooperating community of genes but
X_4_01 — Personalized and Genomic Medicine
Personalized medicine (also called precision medicine) represents the shift from one-size-fits-all treatment to therapies tailored to an individual's genetic profile, biomarkers, and molecular disease characteristics. Th
Z_5_02 — Metagenomics and Environmental DNA
Metagenomics — the sequencing and analysis of genetic material recovered directly from environmental samples without culturing organisms — has revealed that the vast majority of Earth's microbial diversity was invisible
Z_5_09 — Single-Cell Genomics: Profiling Biology One Cell at a Time
Single-cell genomics — the set of technologies that enable the measurement of DNA sequences, RNA expression, protein levels, or epigenetic states in individual cells rather than bulk populations — has revolutionized biol
Z_2_18 — Pharmacogenomics and Precision Medicine
Pharmacogenomics — the study of how genetic variation affects individual responses to drugs — aims to replace the "one-size-fits-all" prescribing model with genotype-guided therapy, selecting the right drug at the right
Z_2_16 — Cancer Genomics & Precision Oncology
Cancer genomics — the comprehensive analysis of the genetic alterations that drive cancer initiation, progression, and resistance to therapy — has transformed oncology from a tissue-of-origin classification system into a
ZB_4_15 — Urban Wildlife Genomics: Rapid Evolution in the Anthropocene City
Cities — covering only ~3% of Earth's land surface but housing >55% of humanity — are emerging as powerful natural laboratories for studying rapid evolution in real time. Urban wildlife genomics investigates how the extr
G_4_21 — Archaeogenomics: Ancient DNA and the Reconstruction of Human History
Archaeogenomics — the extraction, sequencing, and analysis of DNA from ancient biological remains — has revolutionized understanding of human migration, admixture, and population history since Svante Pääbo's pioneering w
L_4_16 — Ancient Pathogen Genomics: Disease DNA from the Archaeological Record
Ancient pathogen genomics — the recovery and analysis of microbial DNA from archaeological remains — has revolutionized understanding of historical pandemics and pathogen evolution. The field was transformed when Johanne
L_4_14 — Ancient Pathogen Genomics
Ancient pathogen genomics — the recovery, sequencing, and analysis of pathogen DNA from archaeological remains — has revolutionized our understanding of past pandemics, pathogen evolution, and human-disease coevolution.
L_2_17 — Pacific Islander Genetics: Austronesian Ancestry, Denisovan Introgression, and Oceanian Genomics
Pacific Islander populations — spanning Melanesia, Micronesia, and Polynesia — harbor some of the most genetically complex and scientifically informative genomes in human biology. Their genetic history records multiple d
L_2_12 — Paleogenomics of Africa: The Cradle Revisited
Africa is the cradle of human evolution — the continent where Homo sapiens originated, where the deepest branches of the human family tree diverge, and where the greatest genetic diversity in our species is found. Yet pa
S_2_12 — Personalized Medicine: Pharmacogenomics and Precision Health
Personalized medicine (also called precision medicine) tailors medical treatment to the individual characteristics of each patient — particularly their genetic makeup, but also incorporating biomarkers, environmental fac
S_2_11 — Bioinformatics: Computational Genomics and Drug Discovery
Bioinformatics — the application of computational methods to biological data — has become indispensable to modern biology and medicine, driven by the exponential growth of genomic, transcriptomic, proteomic, and metabolo
Z_3_04 — Comparative Genomics and Cross-Species Analysis
Comparative genomics — the systematic comparison of genome sequences across species — has become the primary tool for understanding genome evolution, identifying functionally important sequences, and reconstructing the T
Z_2_15 — Future of Genomics and Personalized Medicine
Genomics is undergoing a transition from research tool to clinical infrastructure. The cost of whole-genome sequencing (WGS) has plummeted from $2.7 billion (Human Genome Project, 1990–2003) to ~$200 per genome (Illumina
Z_2_13 — Pharmacogenomics and Personalized Medicine
Pharmacogenomics — the study of how genetic variation influences drug response — is among the most clinically actionable applications of human genetics. Adverse drug reactions (ADRs) are the 4th–6th leading cause of deat
Z_2_03 — Pharmacogenomics & Ethnobotanical Genetics
Pharmacogenomics — the study of how genetic variation affects drug response — has revealed that enzymes governing drug metabolism, particularly the cytochrome P450 (CYP) superfamily, show extraordinary population-specifi
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