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.
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Subcategories
This category has the following 20 subcategories, out of 48 total.
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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 163 pages are in this category, out of approximately 341 total. This list may not reflect recent changes.
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- Macrosatellite
- Magnetogenetics
- MAP3K15
- 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
N
- Nagoya Protocol
- Necrofauna
- Neofunctionalization
- Neurocriminology
- Neurogenetics
- Neurogenomics
- Neuronal lineage marker
- Neutral network (evolution)
- Nic site
- Nik operon
- NIPAL4
- NlaIII
- Non-allelic homologous recombination
- Nondisjunction
- Noninvasive genotyping
- Normalized chromosome value
- Nuclear sexing
- Nuclease protection assay
- Nucleomodulin
P
- Parasitic chromosome
- Partial dominance hypothesis
- Pathogenicity island
- Patome
- Penetrance
- Peptidoglycan recognition protein 3
- Peptidoglycan recognition protein 4
- Phene
- Phenocopy
- Phenotype modification
- Phenotypic integration
- Phenotypic plasticity
- Phylostratum
- PLAC1
- Plant genetic resources
- Plant–fungus horizontal gene transfer
- Polar overdominance
- Polydactyly-myopia syndrome
- Polygenic adaptation
- Polymerase stuttering
- Polyphenism
- Polyploid complex
- Position-effect variegation
- Positional sequencing
- Primosome
- Prion
- Pronucleus
- Proofreading (biology)
- Prophase
- Proton coupled amino acid transporter
- Pseudoalleles
- Pseudolinkage
- PURA syndrome
R
- Radiation reduced hybrid
- Ras-interacting protein 1
- RCCX
- Reading frame
- Reassortment
- RecF pathway
- Reciprocal silencing
- RecLOH
- Recognition sequence
- Red-suffusion rosy-faced lovebird mutation
- Replication protein A
- Reproductive isolation
- Restriction map
- Reverse transcriptase
- Revive & Restore
- Ribosomal frameshift
- Right To Know
- Robustness (evolution)
- Rule of six (viruses)
S
- S4 protein domain
- SBK3
- Scleraxis
- SCRN3
- Sequence space (evolution)
- Sex linkage
- Sex-chromosome dosage compensation
- Sex-linked barring
- Shadow effect
- Signature-tagged mutagenesis
- Ahna Skop
- SMIM15
- Snagger (software)
- Snijders Blok–Campeau syndrome
- Snpstr
- Somatic mutation
- SOS chromotest
- SoxC group
- Staggered extension process
- State switching
- Sterility (physiology)
- Strawberry roan
- Subclade
- SUI1
- SWAP protein domain
- Synaptic tagging
- Syntelic
- Syntelog
- Synthesis-dependent strand annealing
- Synthetic genetic array
- Synthetic lethality
- Synthetic rescue
- Systems Biology Ontology
T
- Tafazzin
- Tandem repeat locus
- Three-point cross
- Transcription bubble
- Transcriptional amplification
- Transcriptome-wide association study
- Transfer DNA binary system
- Transformation efficiency
- Transgressive segregation
- Transmission disequilibrium test
- Tre recombinase
- Triangle of U
- Trinucleotide repeat expansion
- Tumor mutational burden