Category: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.
 |
Wikimedia Commons has media related to Genetics. |
| To display all subcategories click on the "►": |
|---|
Subcategories
This category has the following 51 subcategories, out of 51 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 304 total. This list may not reflect recent changes (learn more).
(previous page) (next page)A
- AB(O)H antigens secretion
- Ac/Ds transposable controlling elements
- Active chromatin sequence
- Additive genetic effects
- 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
B
C
- Candidate gene
- CaSNP
- Cell–cell fusogens
- Chaperone code
- Chemical genetics
- Chi site
- Chiasma (genetics)
- Chimera (EST)
- Chromosome 2q deletion
- Coefficient of coincidence
- Common misunderstandings of genetics
- Complex traits
- Compound heterozygosity
- Congenic
- Constitutive ablation
- Copy number analysis
- Cotransformation
- Countergradient variation
- Cre recombinase
- 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
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 ecology
- Genetic exceptionalism
- Genetic imbalance
- Genetic marker
- Genetic matchmaking
- Genetic memory (biology)
- Genetic predisposition
- Genetic program
- Genetic structure
- Genetic variance
- Genetic viability
- Genetics in fiction
- Genetics nursing
- Genetics of infertility
- Genetics of posttraumatic stress disorder
- Genevestigator
- 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
- Homologous recombination
- Horizontal gene transfer
- Horizontal gene transfer in evolution
- Human Genome Project
- Human germline engineering
- HUMARA assay
- Hybrid speciation
- Hybrizyme
- Hypersensitive site
- Hypervariable
L
M
- Magnetogenetics
- Marker-assisted selection
- MASS syndrome
- Maternal effect
- 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
- Multiple cloning site
N
- Nagoya Protocol
- Necrofauna
- Neofunctionalization
- Neurocriminology
- Neurogenetics
- Neurogenomics
- Neuronal lineage marker
- Neutral network (evolution)
- Nic site
- Nick translation
- Nik operon
- NlaIII
- Non-allelic homologous recombination
- Nondisjunction
- Noninvasive genotyping
- Normalized chromosome value
- Nuclear sexing
- Nuclease protection assay
