Wikipedia:WikiProject Missing encyclopedic articles/Genome Glossary
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This list contains subjects important to genomic research, including that done by the Human Genome Project.
Prior to pruning, this list contained 449 entries. Before removing blue links from this list, please check them to make sure they actually cover the intended subject.
Public domain sources: Human Genome Project glossary, Genome.gov glossary
- acquired genetic mutation
- additive genetic effects
- affected relative pair
- aggregation technique
- allogeneic
- avuncular relationship
- base sequence analysis
- brca1/brca2 -- we have BRCA1 and BRCA2
- cancer
- candidate gene
- capillary array
- carcinogen
- carcinoma
- carrier
- cdna library
- centimorgan
- centromere
- chimera (pl. chimaera)
- chimeraplasty
- chloroplast chromosome
- chromomere
- chromosomal deletion
- chromosomal inversion
- chromosome
- chromosome painting
- chromosome region p
- chromosome region q
- clone
- clone bank
- cloning
- cloning vector
- code
- codominance
- codon
- coisogenic or congenic
- comparative genomics
- complementary dna
- complementary sequence
- complex trait
- computational biology
- confidentiality
- congenital
- conserved sequence
- constitutive ablation
- contig
- contig map
- cosmid
- craniosynostosis
- crossing over
- cystic fibrosis
- cytogenetic map
- cytogenetics
- cytological band
- cytological map
- cytoplasmic (uniparental) inheritance
- cytoplasmic trait
- cytosine
- data warehouse
- deletion
- deletion map
- deoxyribonucleic acid
- deoxyribonucleotide
- deoxyribose
- diabetes mellitus
- diploid
- directed evolution
- directed mutagenesis
- directed sequencing
- disease-associated genes
- dna
- dna bank
- dna probe
- dna repair genes
- dna replication
- dna sequence
- dna sequencing
- domain
- dominant
- double helix
- draft sequence
- duplication
- electrophoresis
- electroporation
- ellis - van creveld syndrome
- embryonic stem (es) cells
- endonuclease
- enzyme
- epistasis
- escherichia coli
- eugenics
- eukaryote
- evolutionarily conserved
- exogenous dna
- exon
- exonuclease
- expressed gene
- expressed sequence tag
- familial mediterranean fever
- fibroblasts
- filial generation
- fingerprinting
- finished dna sequence
- flow cytometry
- flow karyotyping
- fluorescence in situ hybridization
- forensics
- fragile x syndrome
- fraternal twin
- full gene sequence
- functional genomics
- gamete
- gc-rich area
- gel electrophoresis
- gene
- gene amplification
- gene chip technology
- gene expression
- gene family
- gene library
- gene mapping
- gene pool
- gene prediction
- gene product
- gene testing
- gene therapy
- gene transfer
- genetic code
- genetic counseling
- genetic discrimination
- genetic engineering
- genetic engineering technology
- genetic illness
- genetic informatics
- genetic map
- genetic marker
- genetic material
- genetic mosaic
- genetic polymorphism
- genetic predisposition
- genetic screening
- genetic testing
- genetics
- genome
- genome project
- genomic library
- genomic sequence
- genomics
- genotype
- germ cell
- germ line
- germ line gene therapy
- germ line genetic mutation
- guanine
- gyandromorph
- haploid
- haploinsufficiency
- haplotype
- hematopoietic stem cell
- hemizygous
- hemophilia
- hereditary cancer
- heterozygosity
- heterozygote
- heterozygous
- highly conserved sequence
- high-throughput sequencing
- hirschsprung's disease
- holoprosencephaly
- homeobox
- homolog
- homologous chromosome
- homologous recombination
- homology
- homozygote
- homozygous
- human artificial chromosome
- human gene therapy
- human genome initiative
- long-range restriction mapping
- lymphocyte
- macrorestriction map
- malformation
- mapping
- mapping population
- marker
- mass spectrometry
- megabase
- meiosis
- melanoma
- mendel, johann
- mendelian inheritance
- messenger rna
- metaphase
- microarray
- microarray technology
- microbial genetics
- microinjection
- micronuclei
- microsatellite
- mitochondrial dna
- mitosis
- model organisms
- modeling
- molecular biology
- molecular farming
- molecular genetics
- molecular medicine
- monogenic disorder
- monogenic inheritance
- monosomy
- morbid map
- mouse model
- multifactorial or multigenic disorder
- multiple endocrine neoplasia, type 1
- multiplexing
- murine
- mutagen
- mutagenicity
- mutation
- neurofibromatosis
- niemann-pick disease, type c
- nitrogenous base
- non-coding dna
- non-directiveness
- nonsense mutation
- northern blot
- nuclear transfer
- nucleic acid
- nucleolar organizing region
- nucleotide
- nucleus
- oligo
- oligogenic
- oligonucleotide
- oncogene
- oncovirus
- open reading frame
- operon
- overlapping clones
- p1-derived artificial chromosome
- p53
- parkinson's disease
- patent
- pedigree
- penetrance
- peptide
- phage
- pharmacogenomics
- phenocopy
- phenotype
- physical map
- plasmid
- pleiotropy
- pluripotency
- polydactyly
- polygenic disorder
- polymerase chain reaction
- polymerase, dna or rna -- We have DNA polymerase and RNA polymerase
- polymorphism
- polypeptide
- population genetics
- positional cloning
- premature chromosome condensation
- primary immunodeficiency
- primer
- privacy
- probe
- prokaryote
- promoter
- pronucleus
- prostate cancer
- protease
- protein
- proteome
- proteomics
- pseudogene
- purine
- pyrimidine
- radiation hybrid
- rare-cutter enzyme
- recessive
- recessive gene
- reciprocal translocation
- recombinant clone
- recombinant dna
- recombinant dna molecules
- recombinant dna technology
- recombination
- regulatory region or sequence
- repetitive dna
- reporter gene
- repressor
- resolution
- restriction enzyme, endonuclease
- restriction enzymes
- restriction fragment length polymorphism
- restriction-enzyme cutting site
- retroviral infection
- risk communication
- sequencing technology
- sporadic cancer
- suppressor gene
- syngeneic
- targeted mutagenesis
- working draft dna sequence