Category:Genetics
Wikimedia Commons has media related to Genetics.
 | This category is overpopulated. It is suggested that the contents of the category be subcategorized. |
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.
| To display all subcategories click on the "►": |
|---|
Subcategories
This category has the following 49 subcategories, out of 49 total.
*
+
A
- Algae biomass producers (9 P)
- Genetics awards (20 P)
B
C
- Genetics concepts (24 P)
D
E
- Genetics experiments (21 P)
G
- Genetic fallacies (24 P)
H
J
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 (8 P)
Μ
- Genetics images (2 F)
Σ
Pages in category "Genetics"
The following 200 pages are in this category, out of approximately 307 total. This list may not reflect recent changes.
(previous page) (next page)*
A
- Absconditabacterales genetic code
- Ac/Ds transposable controlling elements
- Accessory gene regulator
- Active chromatin sequence
- Additive genetic effects
- Agouti coloration genetics
- Agricultural weed syndrome
- Allelic exclusion
- Allotype (immunology)
- Ambidirectional dominance
- Amelogenin
- Anaerococcus and Onthovivens genetic code
- Genetic analysis
- Antagonistic pleiotropy hypothesis
- Atavism
- Autogamy depression
B
C
- CaSNP
- Cell–cell fusogens
- Centimorgan
- Chaperone code
- Chemical genetics
- Chemogenetics
- Chi site
- Chiasma (genetics)
- Chimera (molecular biology)
- Codon reassignment
- Coefficient of coincidence
- Common misunderstandings of genetics
- Compound heterozygosity
- Congenic
- Constitutive ablation
- Copy number analysis
- Cotransformation
- Countergradient variation
- CRT (genetics)
- Cultural hitchhiking
- Cytodeme
- Cytotaxonomy
D
- De novo domestication
- Deme (biology)
- Dermatoglyphics
- Developmental homeostasis
- Diallel cross
- Direct repeat
- 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
- Enterosoma genetic code
- EPR1
- Evo-devo gene toolkit
- Exome
- Exon skipping
- Exonic splicing enhancer
- Exonic splicing silencer
- Extrachromosomal array
- Extranuclear inheritance
G
- GAL4/UAS system
- Gametic phase
- Gene cassette
- Gene mapping
- Gene orders
- Gene regulatory circuit
- Gene signature
- Gene theft
- Gene transfer agent
- Gene trapping
- Generation of Animals
- Genetic architecture
- Genetic code
- Genetic demixing
- Genetic ecology
- Genetic exceptionalism
- Genetic imbalance
- Genetic interaction network
- Genetic map function
- Genetic matchmaking
- Genetic predisposition
- 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
- Genetics of synesthesia
- Genevestigator
- 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
I
M
- Macrosatellite
- Magnetogenetics
- Marker-assisted selection
- MASS syndrome
- Maternal effect
- Meiotic drive
- Memetics
- Mendelian error
- Microsatellite
- Midparent
- Minichromosome
- Mirror tree
- Mobilome
- Modifications (genetics)
- Molecular cytogenetics
- Morbid map
- Mosaic (genetics)
- Haplogroup Z
- Multifactorial disease
- Museomics
- Mutation accumulation theory