Category:Genetics
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Genetics is the study of genes, heredity, and the variation of organisms, as well as the medical practice of diagnosing, treating, and counseling patients with genetic disorders. Humans began applying knowledge of genetics in prehistory with the domestication and breeding of plants and animals. In modern research, genetics provides important tools in the investigation of the function of a particular gene, e.g. analysis of genetic interactions. Within organisms, genetic information generally is carried in chromosomes, where it is represented in the chemical structure of particular DNA molecules.
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Subcategories
This category has the following 52 subcategories, out of 52 total.
A
B
C
D
E
G
H
L
M
N
O
P
Q
R
S
T
Μ
Σ
Τ
Pages in category "Genetics"
The following 200 pages are in this category, out of approximately 326 total. This list may not reflect recent changes (learn more).
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- Ac/Ds transposable controlling elements
- Active chromatin sequence
- Additive genetic effects
- Agouti coloration genetics
- Aicardi–Goutières syndrome
- Allelic exclusion
- Allotype (immunology)
- Ambidirectional dominance
- Amelogenin
- AMELX
- AMELY
- Aminoacylase 1 deficiency
- Amplified Ribosomal DNA Restriction Analysis
- Aniridia
- Antagonistic pleiotropy hypothesis
- Atavism
- Autogamy depression
B
C
- C14orf119
- C16orf90
- Candidate gene
- CaSNP
- Cell–cell fusogens
- Chaperone code
- Chemical genetics
- Chi site
- Chiasma (genetics)
- Chimera (molecular biology)
- Chromosome 2q deletion
- CLIP4
- Coefficient of coincidence
- Color Genomics
- Common misunderstandings of genetics
- Complex traits
- Compound heterozygosity
- Congenic
- Constitutive ablation
- Copy number analysis
- Cotransformation
- Countergradient variation
- Cre recombinase
- Cultural hitchhiking
- Cytodeme
- Cytotaxonomy
D
E
- Ecogenetics
- Ectoderm specification
- Elective genetic and genomic testing
- Emergenesis
- Emopamil binding protein
- Endoreduplication
- Enhanceosome
- Enhancer trap
- Eukaryotic chromosome fine structure
- Evo-devo gene toolkit
- Exome
- Exon skipping
- Exonic splicing enhancer
- Exonic splicing silencer
- Extrachromosomal array
- Extranuclear inheritance
F
G
- GAL4/UAS system
- Gametic phase
- Gene cassette
- Gene mapping
- Gene orders
- Gene signature
- Gene theft
- Gene transfer agent
- Gene trapping
- Gene–environment correlation
- Genetic analysis
- Genetic architecture
- Genetic carrier
- Genetic code
- Genetic demixing
- Genetic Discrimination Observatory
- Genetic ecology
- Genetic exceptionalism
- Genetic imbalance
- Genetic interaction network
- Genetic marker
- Genetic matchmaking
- Genetic predisposition
- Genetic program
- Genetic structure
- Genetic variance
- Genetic viability
- Genetics in fiction
- Genetics nursing
- Genetics of infertility
- Genetics of post-traumatic stress disorder
- Genevestigator
- Genome informatics
- Genome sequencing of endangered species
- Genome skimming
- Genome-wide CRISPR-Cas9 knockout screens
- Genomic convergence
- Genopolitics
- Genosome
- Genotropism
- Genotype
- Genotype–phenotype distinction
- Genotyping
- Genotyping by sequencing
- Germline mosaicism
- GNC hypothesis
H
- Haploidisation
- Haploinsufficiency
- Haplotype estimation
- Haploid-relative-risk
- Hayflick limit
- Heredity
- Heritability
- Heterogamy
- Hilpda
- Histone H2A.Z
- Horizontal gene transfer
- Horizontal gene transfer in evolution
- HSPB7
- Human epigenome
- Human Genome Project
- Human germline engineering
- Human somatic variation
- HUMARA assay
- Hybrid speciation
- Hybrizyme
- Hypersensitive site
- Hypervariable
I
L
M
- Magnetogenetics
- Marker-assisted selection
- MASS syndrome
- Maternal effect
- Maximum genetic diversity
- Meiotic drive
- Mendelian error
- Microsatellite
- Midparent
- Minichromosome
- Mobilome
- Modifications (genetics)
- Molecular cytogenetics
- Morbid map
- Mosaic (genetics)
- Haplogroup Z
- MtDNA haplogroups in populations of South Asia
- Multifactorial diseases
- Multiple cloning site
- Mutation accumulation theory