Category:Genetics
Wikimedia Commons has media related to 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 46 subcategories, out of 46 total.
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A
- Algae biomass producers (9 P)
- Genetics awards (20 P)
B
C
- Chimerism (9 P)
- Genetics concepts (20 P)
D
E
- Genetics experiments (21 P)
G
H
L
- Genetic linkage analysis (3 P)
M
N
- Nucleobases (38 P)
O
P
Q
- Quantitative trait loci (3 P)
R
- Ribosomopathy (6 P)
S
T
- Genetics terms (9 P)
Μ
- Images of genetic subjects (1 F)
Σ
Pages in category "Genetics"
The following 200 pages are in this category, out of approximately 341 total. This list may not reflect recent changes.
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- Ac/Ds transposable controlling elements
- Accessory gene regulator
- Active chromatin sequence
- Additive genetic effects
- Agouti coloration genetics
- Agricultural weed syndrome
- Aicardi–Goutières syndrome
- Allelic exclusion
- Allotype (immunology)
- Ambidirectional dominance
- Amelogenin
- AMELX
- AMELY
- Aminoacylase 1 deficiency
- Aniridia
- Antagonistic pleiotropy hypothesis
- Atavism
- Autogamy depression
B
C
- C3orf56
- C14orf119
- C16orf90
- C17orf75
- CaSNP
- Cell–cell fusogens
- Centimorgan
- Chaperone code
- Chemical genetics
- Chemogenetics
- Chi site
- Chiasma (genetics)
- Chimera (molecular biology)
- Chromosome 2q deletion
- CLIP4
- Codon reassignment
- Coefficient of coincidence
- Color Genomics
- Common misunderstandings of genetics
- Compound heterozygosity
- Congenic
- Constitutive ablation
- Copy number analysis
- Cotransformation
- Countergradient variation
- CRT (genetics)
- Cultural hitchhiking
- Cytodeme
- Cytotaxonomy
D
- Deme (biology)
- Dermatoglyphics
- Developmental homeostasis
- Diallel cross
- Direct repeat
- Dishevelled binding antagonist of beta catenin 1
- Distal promoter
- Distyly
- Diversity panel
- DNase I hypersensitive site
- Domestication islands
- Domestication syndrome
- Doubled haploidy
- Downregulation and upregulation
- Drifty gene hypothesis
- Drosophila hybrid sterility
- Dynamical genetics
E
- Ectoderm specification
- Elective genetic and genomic testing
- Emergenesis
- Emopamil binding protein
- Endemixit
- 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 regulatory circuit
- Gene signature
- Gene theft
- Gene transfer agent
- Gene trapping
- Genetic analysis
- Genetic architecture
- Genetic code
- Genetic demixing
- Genetic ecology
- Genetic exceptionalism
- Genetic imbalance
- Genetic interaction network
- Genetic matchmaking
- Genetic predisposition
- Genetic program
- Genetic resources
- Genetic resources conservation and sustainable use
- Genetic structure
- Genetic viability
- Genetics
- Genetics in fiction
- Genetics nursing
- Genetics of infertility
- Genetics of post-traumatic stress disorder
- Genevestigator
- Genome India Project
- Genome-wide CRISPR-Cas9 knockout screens
- Genomic convergence
- Genopolitics
- Genosome
- Genotropism
- Genotype
- Genotype–phenotype distinction
- Genotype–phenotype map
- Genotyping by sequencing
- Germline mosaicism
- GNC hypothesis
H
- Halperin-Birk syndrome
- Haploidisation
- Haploinsufficiency
- Haploid-relative-risk
- Hayflick limit
- Heme transporter
- Hereditary carrier
- Heredity
- Heterogamy
- Hilpda
- Horizontal gene transfer in evolution
- Hovlinc
- HSPB7
- Human epigenome
- Human germline engineering
- Human somatic variation
- Hybrid speciation
- Hybrizyme
- Hypersensitive site
- Hypervariable
I
Media in category "Genetics"
This category contains only the following file.
Translocation Down syndrome.png 602 × 392; 50 KB
