Index of genetics articles
Genetics (from Ancient Greek γενετικός genetikos, “genite” and that from γένεσις genesis, “origin”[1][2][3]), a discipline of biology, is the science of heredity and variation in living organisms.[4]
Articles (arranged alphabetically) related to genetics include:
A
    
- Acentric chromosome
 - Achondroplasia
 - Active site
 - Adam's Curse
 - Adaptation
 - Adenine
 - Adenosine
 - Adenovirus
 - Adenosine diphosphate (ADP)
 - Ala
 - Alagille syndrome
 - Albino
 - Alcoholism
 - Alkylating agent
 - Allele
 - Allele frequency
 - Alleles
 - Allopolyploid
 - Allosteric protein
 - Allozyme
 - Alternative splicing
 - Altruism
 - Alu family
 - Alzheimer's disease
 - Amber codon
 - Ames test
 - Amino acid
 - Amino acid sequence
 - Amino acids
 - Amniocentesis
 - Amorph
 - AMP
 - Amphidiploid
 - Amplification
 - Anagenesis
 - Anaphase
 - Aneuploid
 - Aneuploid cell
 - Aneuploidy
 - Angelman syndrome
 - Angiosperm
 - Animal model
 - Annealing
 - Annotation
 - Antibody
 - Anticipation
 - Anticoding strand
 - Anticodon
 - Antigen
 - Antimorph
 - Antiparallel
 - Antisense
 - Antisense RNA
 - Antisense strand
 - Antisense therapy
 - AP endonuclease
 - AP site
 - Apert syndrome
 - Apoptosis
 - Applied genetics
 - Arg
 - Arrayed library
 - Ascospore
 - Ascus
 - Asexual spore
 - Asn
 - Asp
 - Assembly
 - Assortative mating
 - Atavism
 - ATP
 - Attenuator
 - Autogamy
 - Autopolyploid
 - Autoradiograph
 - Autoradiography
 - Autosomal dominant
 - Autosome
 - Autotroph
 - Auxotroph
 - Auxotrophic mutant
 - Axoneme
 
B
    
- B form DNA
 - Bacillus
 - Back mutation
 - Backcross
 - Bacteria
 - Bacterial conjugation
 - Bacterial lawn
 - Bacteriophage
 - Balbiani ring
 - Barr body
 - Basal body
 - Base
 - Base analogue
 - Base pair
 - Base pairs
 - Base sequence
 - Batesian mimicry
 - Bayesian analysis
 - Bead theory
 - Behavioral genetics
 - Behavioural genetics
 - Beta-galactosidase
 - Bimodal distribution
 - Binary fission
 - Binomial expansion
 - Binomial theorem
 - Biochemical genetics
 - Bioinformatics
 - Biolistic
 - Bioremediation
 - Biotechnology
 - Biparental zygote
 - Birth defect
 - Bivalent (genetics)
 - BLAST
 - Blastoderm
 - Blastomere
 - Blastopore
 - Blastula
 - Blending inheritance
 - Blunt-end ligation
 - Bookmarking
 - Brachydactyly
 - Branch migration
 - BRCA1
 - BRCA2
 - Breakage and reunion
 - Bridging cross
 - Bud
 - Buoyant density
 - Burkitt lymphoma
 
C
    
- Cancer
 - Candidate gene
 - Capillary array
 - Carcinogen
 - Carcinoma
 - Carrier
 - Carrier testing
 - Cat coat genetics
 - cDNA
 - cDNA library
 - Cell
 - Centimorgan
 - Central dogma of molecular biology
 - Centromere
 - Chemical base
 - Chimeraplasty
 - Chromomere
 - Chromosomal crossover
 - Chromosomal deletion
 - Chromosome
 - Chromosome aglet
 - Chromosome banding
 - Chromosome painting
 - Chromosome region p
 - Chromosome region q
 - Classical genetics
 - Cleft lip
 - Cleft palate
 - Clinical geneticist
 - Clone (genetics)
 - Clone bank
 - Cloned DNA
 - Cloning
 - Cloning vector
 - Coccus
 - Code
 - Code dictionary
 - Coding strand
 - Codominance
 - Codon
 - Codon usage bias aka Codon preference
 - Cohesive end
 - Cointegrate
 - Col plasmid
 - Colicinogenic factor
 - Colonoscopy
 - Colony
 - Common ancestry
 - Comparative genomics
 - Compartment
 - Competence factor
 - Competent
 - Complementarity genes
 - Complementary DNA
 - Complementation
 - Complementation test
 - Complete linkage
 - Complex trait
 - Component of fitness
 - Composite transposon
 - Concordance
 - Conditional mutation
 - Confidence limits
 - Confidentiality
 - Congenital
 - Conjugation tube
 - Consanguineous
 - Consanguinity
 - Consensus sequence
 - Conservative change
 - Conserved sequence
 - Constant region
 - Constitutive gene
 - Contig
 - Contig map
 - Contig maps
 - Contiguous genes
 - Continuous variation
 - Controlling element
 - Copper fist
 - Copy-choice model
 - Corepressor
 - Cosegregation
 - Cosmid
 - Cosmids
 - Cot value
 - Cotransduction
 - Cotransformation
 - Coupling
 - Covariance
 - cpDNA
 - CpG island
 - Craniosynostosis
 - Cri du chat
 - cRNA
 - Cross
 - Cross-fertilization
 - Crossbreed
 - Crossover
 - Crossover suppressor
 - Crossovers
 - Cryptic coloration
 - Culture
 - Cyclic AMP
 - Cys
 - Cystic fibrosis
 - Cytidine
 - Cytochrome
 - Cytogenetic map
 - Cytogenetics
 - Cytohet
 - Cytokinesis
 - Cytological band
 - Cytological map
 - Cytoplasm
 - Cytoplasmic trait
 - Cytosine
 - Cytosol
 
D
    
- D-loop
 - Darwinian fitness
 - Data warehouse
 - Dauermodification
 - Deficiency
 - Degenerate code
 - Degenerate codon
 - Degrees of freedom (physics and chemistry)
 - Deletion
 - Deletion chromosome
 - Deletion map
 - Deletion mapping
 - Deme (biology)
 - Dementia
 - Denaturation
 - Denaturation map
 - Denominator element
 - Deoxyribonuclease
 - Deoxyribonucleotide
 - Deoxyribose
 - Depauperate fauna
 - Derepressed
 - Determinant
 - Determination
 - Deterministic
 - Developmental biology
 - Diabetes mellitus
 - Diakinesis
 - Dicentric bridge
 - Dicentric chromosome
 - Dictyotene
 - Dideoxy method
 - Differentiation
 - Dihybrid
 - Dihybrid cross
 - Dimerization
 - Dimorphism
 - Dioecious plant
 - Diploid
 - Directed evolution
 - Directed mutagenesis
 - Directed sequencing
 - Directionality (molecular biology)
 - Discrete generations
 - Disease
 - Disruptive selection
 - Distribution
 - DMD
 - DNA
 - DNA bank
 - DNA clone
 - DNA cloning
 - DNA fingerprint
 - DNA glycosylase
 - DNA gyrase
 - DNA hybridization
 - DNA ligase
 - DNA marker
 - DNA polymerase
 - DNA probe
 - DNA repair genes
 - DNA replication
 - DNA sequence
 - DNA sequencing
 - Docking protein
 - Domain
 - Dominance variance
 - Dominant
 - Dominant allele
 - Dominant phenotype
 - Dosage compensation
 - Dose
 - Dot blotting
 - Double crossover (Bad Link)
 - Double digest
 - Double helix
 - Double infection
 - Double reduction
 - Doublesex
 - Down syndrome
 - Downstream
 - Draft sequence
 - Duplicate gene
 - Dwarfism
 - Dyad
 - Dyad symmetry
 - Dystonia
 
E
    
- E (exit site)
 - Ecdysone
 - Ecological genetics
 - Ectopic expression
 - Ectopic integration
 - Electrophoresis
 - Electroporation
 - ELSI
 - Endogenote
 - Endomitosis
 - Endonuclease
 - Endopolyploidy
 - Endosperm
 - Enforced outbreeding
 - Enhancer
 - Enhancer trap
 - Enriched medium
 - Enucleate cell
 - Enzyme
 - Epigenetics
 - Episome
 - Epistasis
 - Equational division
 - Equivalence group
 - Erythrocytes
 - Escherichia coli
 - Ethics
 - Ethidium
 - Euchromatin
 - Eugenics
 - Eukaryote
 - Eukaryotic cell
 - Euploid
 - Euploidy
 - European Journal of Human Genetics
 - Evolution
 - Evolutionary rate
 - Excision repair
 - Exconjugant
 - Exogenote
 - Exogenous DNA
 - Exon
 - Exon shuffling
 - Exonuclease
 - Expected progeny difference
 - Experimental design
 - Expressed gene
 - Expression vector
 - Expressivity (genetics)
 
F
    
- F factor
 - F plus cell
 - F- cell
 - F-duction
 - F-pili
 - F1 generation
 - F2 generation
 - Factorial
 - Familial cancer
 - Familial trait
 - Family selection
 - Fanconi anemia
 - Fate map
 - Fecundity selection
 - Feedback inhibition
 - Fibroblasts
 - Filial generation
 - Filter enrichment
 - Fingerprint
 - Fingerprinting
 - FISH (Fluorescent in situ hybridization)
 - Fitness (W)
 - Fixed allele
 - Fixed breakage point
 - Flow cytometry
 - Flow karyotyping
 - Fluctuation test
 - Fluorescent in situ hybridization
 - FMET
 - Focus map
 - Footprinting
 - Forensics
 - Forward mutation
 - Founder effect
 - Fragile site
 - Fragile X syndrome
 - Frameshift
 - Frameshift mutation
 - Fraternal twin
 - Frequency histogram
 - Fruiting body
 - Full gene sequence
 - Functional allele
 - Functional genomics
 - Fundamental number
 
G
    
- G-banding
 - Galton Laboratory
 - Gamete
 - Gametophyte
 - Gastrulation
 - GC-rich area
 - Gel electrophoresis
 - Gene
 - Gene chip technology
 - Gene cloning
 - Gene complex
 - Gene conversion
 - Gene dose
 - Gene duplication
 - Gene expression
 - Gene family
 - Gene flow
 - Gene frequency
 - Gene fusion
 - Gene interaction
 - Gene library
 - Gene locus
 - Gene map
 - Gene mapping
 - Gene markers
 - Gene mutation
 - Gene orders
 - Gene pair
 - Gene pool
 - Gene prediction
 - Gene product
 - Gene regulatory network
 - Gene testing
 - Gene theft
 - Gene therapy
 - Gene transfer
 - Genetic algorithm
 - Genetic architecture
 - Genetic carrier
 - Genetic code
 - Genetic counseling
 - Genetic deletion
 - Genetic determinism
 - Genetic disorder
 - Genetic dissection
 - Genetic diversity
 - Genetic drift
 - Genetic engineering
 - Genetic genealogy
 - Genetic history of Europe
 - Genetic illness
 - Genetic informatics
 - Genetic linkage map
 - Genetic load
 - Genetic map
 - Genetic marker
 - Genetic material
 - Genetic mosaic
 - Genetic polymorphism
 - Genetic screen
 - Genetic screening
 - Genetic testing
 - Genetic variance
 - Genetic variation
 - Geneticist
 - Genetics
 - Genetics and archaeogenetics of South Asia
 - Genetics experiments
 - Genic balance theory
 - Genome
 - Genome map
 - Genome project
 - Genome screen
 - Genomic library
 - Genomic sequence
 - Genomics
 - Genophore
 - Genotype
 - Germ cell
 - Germ line
 - Germ-line theory
 - Germinal mutation
 - Germline mutation
 - Giemsa stain
 - Gln
 - Glutamic acid
 - Gly
 - God gene
 - Gradient
 - Gray crescent
 - gRNA
 - Ground state
 - Group 1 intron
 - Group II intron
 - Group selection
 - Guanine
 - Guanosine
 - Guide RNA
 - Gynandromorph
 
H
    
- H-Y antigen
 - Haemoglobin (hb)
 - Haemophilia
 - Haplodiploidy
 - Haploid
 - Haploidization
 - Haploinsufficiency
 - Haplotype
 - Hardy–Weinberg law
 - Harlequin chromosome
 - HAT medium
 - Hayflick limit
 - Heat-shock protein
 - Helicase
 - Hemizygous
 - Hemizygous gene
 - Hemophilia
 - Hereditary cancer
 - Hereditary mutation
 - Heredity
 - Heritability
 - Hermaphrodite
 - Heterochromatin
 - Heteroduplex
 - Heteroduplex DNA
 - Heteroduplex mapping
 - Heterogametic sex
 - Heterogamy
 - Genetic heterogeneity
 - Heterokaryon
 - Heterokaryon test
 - Heteroplasmon
 - Heteroplasmy
 - Heterothallic
 - Heterothallic fungus
 - Heterotroph
 - Heterozygosity
 - Heterozygote
 - Heterozygous
 - Heterozygous DNA
 - Hexaploid
 - Hfr cell
 - Human Genome Project
 - HHMI
 - His
 - Histone
 - HnRNA
 - Hogness box
 - Holandric trait
 - Holoenzyme
 - Holoprosencephaly
 - Homeo-box
 - Homeo-domain
 - Homeobox
 - Homeosis
 - Homogametic sex
 - Homolog
 - Homologue
 - Homology
 - Homoplasmy
 - Homothallic
 - Homothallic fungus
 - Homozygote
 - Homozygous
 - Homozygous gene pair
 - Hormone
 - Host range
 - Hot spot
 - Housekeeping genes
 - HUGO
 - Human gene therapy
 - Human genetics
 - Human genome
 - Human Genome Project
 - Huntington's disease
 - Hybrid (biology)
 - Hybrid DNA
 - Hybrid dysgenesis
 - Hybrid plasmid
 - Hybrid zone
 - Hybridoma
 - Hydrogen bond
 - Hydroxyapatite
 - Hypermorph
 - Hyperploid
 - Hypervariable locus
 - Hypervariable region
 - Hypomorph
 - Hypoploid
 - Hypostatic gene
 
I
    
- Ichthyosis
 - Identical twin
 - Identity by descent
 - Identity by type
 - Idiogram
 - Idiotypic variation
 - Idling reaction
 - Ile
 - Imago
 - Immune system
 - immunity
 - Immunoglobulin (Ig)
 - Immunoglobulin gene
 - Immunohistochemistry
 - Immunotherapy
 - Imprinting
 - Indigenous Amerindian genetics
 - In situ
 - Introduction to genetics
 - In vitro
 - In vitro mutagenesis
 - In vivo
 - Inbreeding
 - Incestuous
 - Inclusive fitness
 - Incomplete dominance
 - Inducer
 - Inducible operon
 - Induction
 - Industrial melanism
 - Infectious transfer
 - Informed consent
 - Inherit
 - Inherited
 - Initiation codon
 - Initiation
 - Initiation
 - Initiator protein
 - Inosine
 - Insertion
 - Insertional mutation
 - Inside marker
 - Intercalating agent
 - Interference
 - Interkinesis
 - Interphase
 - Interrupted mating
 - Intersex
 - Interstitial region
 - Intron
 - Introns
 - Inversion
 - Iojap
 - Ionizing radiation
 - IR
 - IS
 - IS element
 - Isoaccepting tRNA
 - Isochromosome
 - Isoenzyme
 - Isoschizomer
 - Isotope
 - Isozyme
 
J
    
    
K
    
    
L
    
- Lac operon
 - Lagging strand
 - Lambda dgal
 - Lambda phage
 - Lateral inhibition
 - Lawn
 - Leader peptide gene
 - Leader sequence (mRNA)
 - Leader transcript
 - Leading strand
 - Leaky mutant
 - Lesion
 - Lethal gene
 - Leu
 - Leucine zipper
 - Leukemia
 - Li-Fraumeni syndrome
 - Library (genetics)
 - Ligase
 - Line
 - Linear tetrad
 - Linkage
 - Linkage analysis
 - Linkage equilibrium
 - Linkage group
 - Linkage map
 - Linking number
 - Locus
 - Lod score
 - Lod score method
 - Lymphocyte
 - Lymphoma
 - Lyon hypothesis
 - Lys
 - Lysate
 - Lysis
 - Lysogen
 - Lysogenic
 - Lysogenic bacterium
 
M
    
- Macromolecule
 - Macrorestriction map
 - Malformation
 - Manx
 - Mapping
 - Mapping function
 - Mapping population
 - Marfan syndrome
 - Marker
 - Marker retention
 - Mass spectrometry
 - Mate-killer
 - Maternal effect
 - Maternal inheritance
 - Mating type
 - Mean
 - Medium
 - Megabase
 - Meiocyte
 - Meiosis
 - Meiospore
 - Melanoma
 - Melting of DNA
 - Mendel's first law
 - Mendel's second law
 - Mendelian ratio
 - Merozygote
 - Messenger RNA
 - Met
 - Metabolism
 - Metafemale
 - Metagon
 - Metamale
 - Metamere
 - Metaphase
 - Metaphase plate
 - Metastasis
 - Methylation
 - Metrical variation
 - Microarray
 - Microbial genetics
 - Microinjection
 - Micronuclei
 - Microsatellite
 - Microtubules
 - Midparent value
 - Migration
 - Mimicry
 - Minimal medium
 - Mismatch repair
 - Missense mutation
 - Mitochondrial DNA
 - Mitochondrial Eve
 - Human mitochondrial genetics
 - Mitochondrion
 - Mitosis
 - Mitotic apparatus
 - Mitotic crossover
 - Mixed codon family
 - Mode
 - Model organisms
 - Modeling
 - Modifier gene
 - Molecular biology
 - Molecular chaperone
 - Molecular farming
 - Molecular genetics
 - Molecular imprinting
 - Molecular medicine
 - Molecule
 - Monocistronic mRNA
 - Monoclonal antibody
 - Monoecious plant
 - Monogenic disorder
 - Monohybrid
 - Monohybrid cross
 - Monoploid
 - Monosomic
 - Monosomy
 - Morbid map
 - Morphogenesis
 - Mosaic (genetics)
 - Mosaicism
 - Mouse model
 - mRNA
 - mtDNA
 - Mu particle
 - Mu phage
 - Mullerian mimicry
 - Multifactorial
 - Multihybrid
 - Multimeric structure
 - Multiple allelism
 - Multiplexing
 - Murine
 - Mutability
 - Mutagen
 - Mutagenicity
 - Mutant
 - Mutant allele
 - Mutant screening
 - Mutant site
 - Mutation
 - Mutation breeding
 - Mutation event
 - Mutation frequency
 - Mutation rate
 - Mutational load
 - Mutator mutation
 - Muton
 - Myeloma
 - Myotonic dystrophy
 
N
    
- N segment
 - N-end rule
 - Narrow heritability
 - Natural selection
 - Negative control
 - Neo-Darwinism
 - Neomorph
 - Neoplasm
 - Neurofibromatosis
 - Neurospora
 - Neutral mutation
 - Neutral petite
 - Newborn screening
 - NF
 - Nickase
 - Nicking
 - NIH
 - Nitrogen base
 - Nitrogenous base
 - Non-coding DNA
 - Non-coding strand
 - Non-directiveness
 - Non-disjunction
 - Non-histone protein
 - Non-linear tetrad
 - Non-Mendelian ratio
 - Non-parental
 - Non-recombinant
 - Nonsense codon
 - Nonsense mutation
 - Nonsense suppressor
 - Noonan syndrome
 - Norm of reaction
 - Normal distribution
 - Northern analysis
 - Northern blot
 - NPD
 - Nu body
 - Nuclear transfer
 - Nuclease
 - Nucleic acid
 - Nucleoid
 - Nucleolar organizer
 - Nucleolus
 - Nucleoprotein
 - Nucleoside
 - Nucleosome
 - Nucleotide
 - Nucleotide pair
 - Nucleotides
 - Nucleus
 - Null allele
 - Null hypothesis
 - Nullisomic
 - Numerator element
 - Nurse cell
 
O
    
- Ochre codon
 - Okazaki fragment
 - Oligo
 - Oligogenic
 - Oligonucleotide
 - Oncogene
 - Oncogenes
 - Oncovirus
 - Oocyte
 - Oogenesis
 - Oogonia
 - Opal codon
 - Open reading frame
 - Operator (biology)
 - Operon
 - Organelle
 - Organogenesis
 - Outbreeding
 - Outside markers
 - Overdominance
 - Overlapping clones
 - Ovum
 
P
    
- P (peptidyl) site
 - P element
 - P1
 - P53
 - Palindrome
 - Panmictic
 - Paralogous genes
 - Paramecin
 - Parameters
 - Parental
 - Parental ditype
 - Parental imprinting
 - Parkinson's disease
 - Parthenogenesis
 - Partial digest
 - Partial diploid
 - Partial dominance
 - Pascal's triangle
 - Patent
 - Path diagram
 - Pathogen
 - Pattern formation
 - PCR
 - PD
 - Pedigree
 - Penetrance
 - Peptide
 - Peptide bond
 - Peptidyl transferase
 - Permissive condition
 - PEST hypothesis
 - Petite mutation
 - Phage
 - Pharmacogenomics
 - Pharming (genetics)
 - Phe
 - Phenocopy
 - Phenotype
 - Phenotypic variance
 - Phenylketonuria
 - Pheromone
 - Phosphodiester bond
 - Photoreactivation
 - Phyletic evolution
 - Phyletic gradualism
 - Phylogenetic tree
 - Phylogenetics
 - Physical map
 - Piebald
 - Pilus
 - PKU
 - Plant breeding
 - Plasmid
 - Plastid
 - Pleiotropic mutation
 - Pleiotropy
 - Pluripotency
 - Point mutation
 - Poisson distribution
 - Poky mutation
 - Polar body
 - Polar granules
 - Polar mutation
 - Polar overdominance
 - Polarity
 - Polarity gene
 - Pollen grain
 - Poly(A) tail
 - Polyacrylamide
 - Polycistronic
 - Polycistronic mRNA
 - Polydactyly
 - Polygene
 - Polygenic disorder
 - Polymerase
 - Polymerize
 - Polymorphism
 - Polypeptide
 - Polyploid
 - Polyribosome
 - Polysaccharide
 - Polysome
 - Polytene chromosome
 - Population
 - Population bottleneck
 - Population genetics
 - Position effect
 - Positional cloning
 - Positive control
 - Pre-mRNA
 - Precancerous polyp
 - Predisposition
 - Preemptor stem
 - Prenatal diagnosis
 - Pribnow box
 - Primary oocyte
 - Primary spermatocyte
 - Primary structure
 - Primary transcript
 - Primase
 - Primer
 - Primosome
 - Prion
 - Privacy
 - Pro
 - Probability
 - Probability theory
 - Proband
 - Probe
 - Processivity
 - Product of meiosis
 - Product rule
 - Proflavin
 - Progeny testing
 - Prognosis
 - Prokaryote
 - Prokaryotic cell
 - Promoter
 - Pronucleus
 - Proofread
 - Proofreader genes
 - Prophage
 - Prophase
 - Prophylactic surgery
 - Proplastid
 - Propositus
 - Prostate cancer
 - Protease
 - Protein
 - Protein product
 - Protein splicing
 - Proteome
 - Proteomics
 - Proteus syndrome
 - Proto-oncogene
 - Protoplast
 - Prototroph
 - Provirus
 - Pseudoallele
 - Pseudoautosomal region
 - Pseudodominance
 - Pseudogene
 - Public policy
 - Punnett square
 - Purine
 - Purines
 - Pyrimidine
 
R
    
- R factor
 - R plasmid
 - Radiation hybrid
 - RAM mutation
 - Random genetic drift
 - Random mating
 - Rare-cutter enzyme
 - Reading frame
 - Readthrough
 - Reannealing
 - Rec system
 - Receptor element
 - Recessive allele
 - Recessive gene
 - Recessive phenotype
 - Reciprocal altruism
 - Reciprocal cross
 - Recombinant
 - Recombinant clone
 - Recombinant DNA
 - Recon
 - Reduction division
 - Redundant DNA
 - Regression
 - Regulator element
 - Regulator gene
 - Relaxed mutant
 - Renal cell cancer
 - Renal cell carcinoma
 - Renner complex
 - Repeat sequences
 - Repetitive DNA
 - Replica plating
 - Replication fork
 - Replicon
 - Replisome
 - Reporter gene
 - Repressible operon
 - Repression
 - Repressor
 - Reproductive cells
 - Reproductive success
 - Repulsion (genetics)
 - Restriction digest
 - Restriction enzyme
 - Restriction enzymes
 - Restriction map
 - Retinitis pigmentosa
 - Retinoblastoma
 - Retroviral infection
 - Retrovirus
 - Reverse genetics
 - Reversion
 - RF
 - RFLP
 - RFLP mapping
 - Rho
 - Ribonucleic acid
 - Ribonucleotide
 - Ribose
 - Ribosomal protein
 - Ribosomal RNA
 - Ribosome
 - Ribosomes
 - Ribozyme
 - Risk communication
 - RNA
 - RNA editing
 - RNA phage
 - RNA polymerase
 - RNA replicase
 - RNA splicing
 - Robertsonian fusion
 - rRNA
 - Rule of segregation
 
S
    
- S (Svedberg unit)
 - S-9 mix
 - Sanger sequence
 - Sanger sequencing
 - Sarcoma
 - Satellite
 - Satellite chromosome
 - Satellite DNA
 - Scaffold
 - Scanning hypothesis
 - Scientific method
 - Screening
 - Screening technique
 - Second-site mutation
 - Secondary oocyte
 - Secondary structure
 - Sedimentation
 - Segmentation (biology)
 - Segregation
 - Segregational load
 - Segregational petite
 - Selection
 - Selection progress
 - Selective medium
 - Selective neutrality
 - Selective system
 - Self
 - Self-assembly
 - Self-fertilization
 - Selfed
 - Selfish DNA
 - Sense strand
 - Sequence
 - Sequence assembly
 - Sequence tagged site
 - Sequencing
 - Sex chromosome
 - Sex chromosomes
 - Sex determination
 - Sex linkage
 - Sex linked
 - Sex reversal
 - Sex switch
 - Sex-controlled trait
 - Sex-influenced trait
 - Sex-lethal
 - Sex-limited trait
 - Sex-linked
 - Sex-ratio phenotype
 - Sexduction
 - Sexual selection
 - Sexual spore
 - Shotgun method
 - Shotgun sequencing
 - Shotgun technique
 - Shuttle vector
 - Siblings(sibs)
 - Sickle-cell disease (Sickle cell anemia)
 - Sigma factor
 - Signal hypothesis
 - Signal peptide
 - Signal peptide
 - Silent gene
 - Silent mutation
 - SINE
 - Single-gene disorder
 - Sister chromatids
 - Skew
 - Smooth endoplasmic reticulum
 - SNP
 - SnRNP
 - Sociobiology
 - Solenoid structure
 - Somatic cell
 - Somatic cell hybrid
 - Somatic cells
 - Somatic doubling
 - Somatic mutation
 - Somatic mutations
 - Somatostatin
 - SOS box
 - SOS repair
 - SOS response
 - Southern blot
 - Southern blotting
 - Spacer DNA
 - Speciation
 - Speciation (genetic algorithm)
 - Species
 - Specific-locus test
 - Spectral karyotype
 - Sperm
 - Spermatid
 - Spermatocyte
 - Spermatogenesis
 - Spermatogonium
 - Spermatozoon
 - Spermiogenesis
 - Spina bifida
 - Spindle
 - Spiral cleavage
 - Spirillum
 - Splice site
 - Spliceosome
 - Spontaneous mutation
 - Sporadic cancer
 - Spore
 - Sporophyte
 - Staggered cuts
 - Standard deviation
 - Statistic
 - Statistics
 - Stem cell
 - Stem-loop structure
 - Steroid receptor
 - Stochastic
 - Strain
 - Stringent factor
 - Stringent response
 - Structural gene
 - Structural genomics
 - Substantial equivalence
 - Substitution
 - Subvital gene
 - Suicide gene
 - Supercoil
 - Supercoiling
 - Supergene
 - Superinfection
 - Supersuppressor
 - Suppressive petite
 - Suppressor gene
 - Suppressor mutation
 - Svedberg unit
 - Swivelase
 - Sympatric speciation
 - Synapsis
 - Synaptonemal complex
 - Syncytial blastoderm
 - Syncytium
 - Syndrome
 - Synexpression
 - Syngeneic
 - Synteny
 - Synteny test
 - Synthetic medium
 
T
    
- T-cell receptor
 - T-DNA
 - TACTAAC box
 - Tandem duplication
 - Target theory
 - Targeted mutagenesis
 - TATA box
 - Tautomeric shift
 - Tay–Sachs disease
 - Technology transfer
 - Telomerase
 - Telomere
 - Telophase
 - Temperate phage
 - Template strand
 - Teratogen
 - Teratogenic
 - Teratogens
 - Terminal redundancy
 - Terminator sequence
 - Tertiary structure
 - Test cross
 - Tetrad
 - Tetrad analysis
 - Tetraparental mouse
 - Tetraploid
 - Tetratype (T)
 - Theta structure
 - Thr
 - Three-point cross
 - Thymidine
 - Thymine
 - Thymine dimer
 - Ti plasmid
 - Topoisomer
 - Topoisomerase
 - Totipotency
 - Totipotent
 - Toxicogenomics
 - Trait (biological)
 - Trans
 - Trans conformation
 - Trans-acting
 - Transcription
 - Transcription factor
 - Transcriptome
 - Transducing particle
 - Transduction
 - Transfection
 - Transfer RNA
 - Transferase
 - Transform
 - Transformation
 - Transformer
 - Transgenic
 - Transgenic organism
 - Transgressive phenotype
 - Transient diploid
 - Transition
 - Transition mutation
 - Translation
 - Translocase (EF-G)
 - Translocation
 - Transposable element
 - Transposition
 - Transposon
 - Transversion
 - Trihybrid
 - Triplet
 - Triplet code
 - Triploid
 - Trisomic
 - Trisomy
 - Tritium
 - tRNA
 - Trp
 - True heritability
 - True speciation
 - Truncation selection
 - Tumour
 - Tumour virus
 - Turner syndrome
 - Twin spot
 - Twin study
 - Two-point cross
 - Type I and type II errors
 - Typological thinking
 - Tyr
 
U
    
- Uncharacterized LOC644249 gene
 - Underdominance
 - Unequal crossover
 - Uninemic chromosome
 - Uniparental disomy
 - Unique DNA
 - Unmixed codon family
 - Unstable mutation
 - Unusual bases
 - Upstream and downstream (DNA)
 - Uptake signal sequence
 - Uracil
 - Uridine
 
V
    
- V-J joining
 - Val
 - Variable region
 - Variance
 - Variate
 - Variegation
 - Vector
 - Viability
 - Virion
 - Viroid
 - Virulent phage
 - Virus
 - VNTR
 
X
    
    
Y
    
    
References
    
    
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