- List of genetic engineering topics
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3' end --5' end --A
Acentric chromosome --Achondroplasia --Active site -- "Adam's Curse " --
Adaptation --Adenine --Adenosine --Adenosine diphosphate --Adenovirus --
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 --Arginine --
Arrayed library --Ascospore --Ascus --Asexual spore --Asn --
Asp --
Assembly --Assortative mating --Asymptomatic carrier --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 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 --Biochemistry --Bioengineering --Bioinformatics --Biolistic --Biology --Bioremediation --Biotechnology --Biparental zygote --Birth defect --Bivalent (genetics) --BLAST --Blastoderm --Blastomere --Blastopore --Blastula --Blending inheritance --Blunt-end ligation --Bookmarking -- Bottleneck --Brachydactyly --Branch migration --BRCA1 --BRCA2 --Breakage and reunion --Bridging cross --Bud --Buoyant density --Burkitt lymphoma --C
Cambridge Reference Sequence --Cancer --Candidate gene --Capillary array --Carcinogen --Carcinoma --
Carrier --Carrier testing --cDNA --cDNA library --
Cell --Cell nucleus --Centimorgan --Central dogma of molecular biology --Centromere --Chemical base --Chimeraplasty --Chromomere --Chromosomal deletion --Chromosome --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 --Cohesive end --Cointegrate --Col plasmid --Colicinogenic factor --Colinearity --Colony --Common ancestry --Comparative genomics --Compartment --Competence factor --
Competent --
Complementarity --Complementary DNA --
Complementation --
Complementation test --Complete linkage --Complex trait --Component of fitness --Composite transposon --
Concordance --Conditional mutation --Confidence limits --Confidentiality --Congenital --Conjugation (genetics) --Conjugation tube --Consanguineous --Consanguinity --Consensus sequence --Conservative change --Conserved sequence --Constant region --
Constitutive --Contig --Contig map --Contig maps --Contiguous genes --Continuous variation --Controlling element --Copper fist --Copy-choice model --Corepressor --
Correction --Cosegregation --Cosmid --Cosmids --Cot value --Cotransduction --Cotransformation --
Coupling --Covariance --cpDNA --CpG island --Craniosynostosis --Cri du chat --
cRNA --Cross --Cross-fertilization --Crossbreed --Crossing over --
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 --
Development --Diabetes mellitus --Diakinesis --Dicentric chromosome --Dictyotene --Dideoxy method --Differentiation --Dihybrid --Dihybrid cross --Dimerization --
Dimorphism --Dioecious plant --Diploid --Directed evolution --Directed mutagenesis --Directed sequencing --Discrete generations --Disease --Disruptive selection --
Distribution --
DMD --DNA --DNA amplification --DNA bank --DNA clone --DNA cloning --DNA electrophoresis --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 --
DOE --Dominance variance --Dominant --Dominant allele --Dominant phenotype --Dosage compensation --Dose --Dot blotting --Double crossover (genetics) --Double digest --Double helix --Double hybrid --Double infection --Double reduction --Doublesex --Down syndrome --Downstream --Draft sequence --Drift --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 --Engineering --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 --Evolution --Evolutionary rate --Excision repair --Exconjugant --Exogenote --Exogenous DNA --Exon --Exon shuffling --Exonuclease --Experimental design --Expressed gene --Expression vector --Expressivity --F
F factor --F plus cell --F- cell --F-duction --F-pili --F1 generation --F2 generation --Factorial --Familial cancer --Familial trait --Family selection --Fanconi's anemia --Fate map --Fecundity selection --Fibroblasts --Filial generation --Filter enrichment --Fimbriae --Fixed allele --Fixed breakage point --Flow cytometry --Flow karyotyping --Fluctuation test --Fluorescent in situ hybridization --FMET --Focus map --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 --Gamete --Gametic selection --Gametophyte --Gastrulation --GC-rich area --Gel electrophoresis --Gene --Gene amplification --Gene chip technology --Gene cloning --Gene complex --Gene conversion --Gene dose --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 pair --Gene pool --Gene prediction --Gene product --Gene regulatory network --Gene testing --Gene therapy --Gene transfer --Genetic algorithm --Genetic architecture --Genetic code --Genetic counseling --Genetic deletion --Genetic determinism --Genetic disorder --Genetic dissection --Genetic engineering --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 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 choice technology --Germinal mutation --Germline mutation --Giemsa stain --Gln --Glu --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 --Heterogamy --Heterogeneity --Heterokaryon --Heterokaryon test --Heteroplasmon --Heteroplasmy --Heterothallic --Heterothallic fungus --Heterotroph --Heterozygosity --Heterozygote --Heterozygous --Heterozygous DNA --Hexaploid --Hfr --HGP --HHMI --Himalayan --Histone --HnRNA --Hogness box --Holandric trait --Holoenzyme --Holoprosencephaly --Homeo-box --Homeo-domain --Homeobox --Homeosis --
Homology --Homoplasmy --Homothallic --Homothallic fungus --Homozygote --Homozygous --Homozygous gene pair --Hormone --Host range --Housekeeping gene --HUGO --Human gene therapy --Human genetic engineering --Human genetics --Human genome --Human Genome Project --Human mitochondrial genetics --Huntington's disease --
Hybrid --Hybrid DNA --Hybrid dysgenesis --Hybrid plasmid --Hybrid zone --
Hybridization --
Hybridize --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 --Ig --Ile --Imago --Immune system --
Immunity --Immunoglobulin (Ig) --Immunoglobulin gene --Immunohistochemistry --Immunotherapy --Imprinting --In situ --In vitro --In vitro mutagenesis --In vivo --Inclusive fitness --Incomplete dominance --Inducer --Inducible operon --
Induction --Industrial melanism --Infectious transfer --Informatics --Inherit --Inherited --Initiation codon --Initiation complex --Initiator protein --Inosine --
Insertion --Insertional mutation --Inside marker --Intercalating agent --Interference --Interkinesis --Interphase --Intron --Introns --Inversion --Ionizing radiation --IS element --Isoaccepting tRNA --Isochromosome --Isoenzyme --Isoschizomer --Isotope --Isozyme --J
Junk DNA --K
Kappa particle --Karyokinesis --Karyotype --Kilobase --Kin selection --Kinetochore --Klinefelter syndrome --L
Lac operon --Lagging strand --Lambda dgal --Lambda phage --Lateral inhibition --Leader peptide gene --Leader sequence --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 --Lligase --Localize --
Locus --Lod score --Lod score method --Lymphocyte --Lymphoma --Lyon hypothesis --Lysate --Lysine --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 --Mitochondrion --Mitosis --Mitotic apparatus --Mitotic crossover --Mixed codon family --Mode --Model organisms --
modelingModifier 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 --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 --Nanobiotechnology --Nanotechnology --Narrow heritability --Natural selection --Negative control --Neo-darwinism --Neomorph --Neoplasm --Neurofibromatosis --Neurospora --Neutral mutation --Neutral petite --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-recombinant --Nonsense codon --Nonsense mutation --Nonsense suppressor --Noonan syndrome --Norm of reaction --Normal distribution --Northern analysis --Northern blot --NPD --Nu body --Nuclear transfer --
Nucleus --Nuclease --Nucleic acid --Nucleoid --Nucleolar organizer --Nucleolus --Nucleoprotein --Nucleoside --Nucleosome --Nucleotide --Nucleotide pair --Nucleotides --Null allele --Null hypothesis --Nullisomic --Numerator element --Nurse cell --O
Ochre codon --Octad --Okazaki fragment --Oligo --Oligogenic --Oligonucleotide --Oncogene --Oncogenes --Oncovirus --Oocyte --Oogenesis --Oogonia --Opal codon --Open reading frame --Operator --Operon --Organelle --Organogenesis --Outbreeding --Outside markers --Overdominance --Overlapping clones --Ovum --P
P (peptidyl) site --P element --P1 --P53 --Palindrome --Panmictic --Parahuman --Paralogous genes --Paramecin --Parameter --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 --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 --Plate --Pleiotropic mutation --Pleiotropy --Pluripotency --Point mutation --Poisson distribution --Poky mutation --Polar body --Polar granules --Polar mutation --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 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 --Probability --Probability theory --Processivity --Product of meiosis --Product rule --Proflavin --Prognosis --Prokaryote --Prokaryotic cell --Promoter --Pronucleus --Proofreader genes --Prophage --Prophase --Proplastid --Propositus --Prostate cancer --Protease --Protein --Protein engineering --Protein product --Proteome --Proteomics --Proteus syndrome --Proto-oncogene --Protoplast --Prototroph --Provirus --Pseudoallele --Pseudoautosomal gene --Pseudodominance --Pseudogene --Public policy --Punnett square --Purine --Purines --Pyrimidine --Q
Quaternary structure --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 --Recessive allele --Recessive gene --Recessive phenotype --Reciprocal altruism --Reciprocal cross --Recombinant --Recombinant clone --Recombinant DNA --Recombination --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 --Reprogenetics --Repulsion --Resolving power --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 --Robertsonian fusion --rRNA --S
S (Svedberg unit) --S-9 mix --Sanger sequence --Sanger sequencing --SAR --Sarcoma --Satellite chromosome --Satellite DNA --Scaffold --Scanning hypothesis --Scientific method --Screening --Screening technique --Second-site mutation --Secondary oocyte --Secondary structure --Sector disambig needed --Sedimentation --Segmentation (biology) --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-limited genes --Sex-limited trait --Sex-linked --Sex-ratio phenotype --Sexual selection --Sexual spore --Shotgun method --Shotgun sequencing --Shotgun technique --Shuttle vector --Siblings(sibs) --Sickle-cell disease --Sigma factor --Signal hypothesis --Signal peptide --Signal sequence --Silent gene --Silent mutation --Single-gene disorder --Sister chromatids --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 --Species --Specific-locus test --Spectral karyotype --Sperm --Spermatid --Spermatocyte --Spermatogenesis --Spermatogonium --Spermatozoon --Spermiogenesis --Spina bifida --Spindle --Spiral cleavage --Spirillum --Splice site --Spliceosome --Splicing --Spontaneous mutation --Sporadic cancer --Spore --Sporophyte --Stacking --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 --Sum rule --Supercoil --Supercoiling --Supergene --Superinfection --Supersuppressor --Suppressive petite --Suppressor gene --Suppressor mutation --Svedberg unit --Swivelase --Sympatric speciation --Synapsis --Synaptonemal complex --Syncytial blastoderm --Syncytium --Syndrome --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 --Template strand --Teratogen --Teratogenic --Teratogens --Terminal redundancy --Terminator sequence --Tertiary structure --Test cross --Tester --Tetracycline Controlled Transcriptional Activation --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 --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 --Tyrosine --U
Underdominance --Unequal crossover --Uninemic chromosome --Uniparental disomy --Unique DNA --Unstable mutation --Unusual bases --Upstream --Uracil --URF --Uridine --V
V-J joining --Val --Variable --Variable region --Variance --Variant --Variate --Variation --Variegation --
Vector --Viability --Virion --Viroid --Virulent phage --Virus --VNTR --W
Wahlund effect --Weismann barrier --Western blot --Wilms' tumor --Wobble --Wolfram syndrome --X
X chromosome --X hyperactivation --X linkage --X linked --X-and-Y linkage --X-inactivation -- --Xenograft --XYY --XYY syndrome --Y
Y chromosome --Y linkage --Y linked --Y-chromosomal Aaron --Y-chromosomal Adam --YAC --Z
Z-DNA --Zinc finger --Zinc-finger protein --Zygote --
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