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Genome Wide Association Studies -- See Genome-Wide Association Study


An analysis comparing the allele frequencies of all available (or a whole GENOME representative set of) polymorphic markers in unrelated patients with a specific symptom or disease condition, and those of healthy controls to identify markers associated with a specific disease or condition 		  1
 

Genome-Wide Association Study -- See Also Genotyping Techniques


Methods used to determine individuals' specific ALLELES or SNPS (single nucleotide polymorphisms) 		  1
Genome-Wide Association Study   2
Genome-Wide Association Study -- methods   2
  Genomes -- 8 Related Subjects   8
Genomes.   144
Genomes -- Analysis   5
 

Genomes, Archaeal -- See Genome, Archaeal


The genetic complement of an archaeal organism (ARCHAEA) as represented in its DNA 		  1
 

Genomes, Bacterial -- See Genome, Bacterial


The genetic complement of a BACTERIA as represented in its DNA 		  1
Genomes -- Congresses   6
Genomes -- Data processing   3
Genomes -- Data processing -- Periodicals   2
 

Genomes Effect of chemicals on -- See Chemogenomics


  1
 

Genomes Effect of drugs on -- See Pharmacogenomics


  1
 

Genomes, Fungal -- See Genome, Fungal


The complete gene complement contained in a set of chromosomes in a fungus 		  1
Genomes -- History. : From biotechnology to genomes : the meaning of the double helix / Philippe Goujon  2001 1
 

Genomes, Human -- See Genome, Human


The complete genetic complement contained in the DNA of a set of CHROMOSOMES in a HUMAN. The length of the human genome is about 3 billion base pairs 		  1
Information storage and retrieval systems -- Genomes.   2
 

Genomes, Insect -- See Genome, Insect


The genetic complement of an insect (INSECTS) as represented in its DNA 		  1
 

Genomes, Microbial -- See Genome, Microbial


The genetic complement of a microorganism as represented in its DNA or in some microorganisms its RNA 		  1
Genomes -- Periodicals   22
 

Genomes, Plant -- See Genome, Plant


The genetic complement of a plant (PLANTS) as represented in its DNA 		  1
 

Genomes Research -- See Genomics


  1
 

Genomes, Viral -- See Genome, Viral


The complete genetic complement contained in a DNA or RNA molecule in a virus 		  1
 

Genomic banks -- See Gene libraries


  1
 

Genomic, Community -- See Metagenomics


The genomic analysis of assemblages of organisms 		  1
 

Genomic, Comparative -- See Genomics


The systematic study of the complete DNA sequences (GENOME) of organisms 		  1
 

Genomic, Environmental -- See Metagenomics


The genomic analysis of assemblages of organisms 		  1
 

Genomic Hybridization -- See Nucleic Acid Hybridization


Widely used technique which exploits the ability of complementary sequences in single-stranded DNAs or RNAs to pair with each other to form a double helix. Hybridization can take place between two complimentary DNA sequences, between a single-stranded DNA and a complementary RNA, or between two RNA sequences. The technique is used to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. (Kendrew, Encyclopedia of Molecular Biology, 1994, p503) 		  1
 

Genomic Hybridization, Comparative -- See Comparative Genomic Hybridization


A method for comparing two sets of chromosomal DNA by analyzing differences in the copy number and location of specific sequences. It is used to look for large sequence changes such as deletions, duplications, amplifications, or translocations 		  1
 

Genomic Hybridizations -- See Nucleic Acid Hybridization


Widely used technique which exploits the ability of complementary sequences in single-stranded DNAs or RNAs to pair with each other to form a double helix. Hybridization can take place between two complimentary DNA sequences, between a single-stranded DNA and a complementary RNA, or between two RNA sequences. The technique is used to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. (Kendrew, Encyclopedia of Molecular Biology, 1994, p503) 		  1
 

Genomic Hybridizations, Comparative -- See Comparative Genomic Hybridization


A method for comparing two sets of chromosomal DNA by analyzing differences in the copy number and location of specific sequences. It is used to look for large sequence changes such as deletions, duplications, amplifications, or translocations 		  1
 

Genomic Imprinting -- See Also DNA Methylation


Addition of methyl groups to DNA. DNA methyltransferases (DNA methylases) perform this reaction using S-ADENOSYLMETHIONINE as the methyl group donor 		  1
Genomic imprinting.   7
Genomic imprinting -- Laboratory manuals   2
 

Genomic Instabilities -- See Genomic Instability


An increased tendency of the GENOME to acquire MUTATIONS when various processes involved in maintaining and replicating the genome are dysfunctional 		  1
Genomic Instability   6
Genomic Instability -- genetics : Genome instability and transgenerational effects / Igor Kovalchuk and Olga Kovalchuk, editors  2010 1
  Genomic libraries -- 2 Related Subjects   2
  Genomic Library -- 2 Related Subjects   2
Genomic Library   13
 

Genomic, Population -- See Metagenomics


The genomic analysis of assemblages of organisms 		  1
 

Genomic probes -- See DNA probes


  1
 

Genomic Science Program (U.S.) -- See Also the earlier heading United States. Department of Energy. Genomics:GTL


  1
 

Genomic Segmental Duplication -- See Segmental Duplications, Genomic


Low-copy (2-50) repetitive DNA elements that are highly homologous and range in size from 1000 to 400,000 base pairs 		  1
 

Genomic Segmental Duplications -- See Segmental Duplications, Genomic


Low-copy (2-50) repetitive DNA elements that are highly homologous and range in size from 1000 to 400,000 base pairs 		  1
 

Genomic Stabilities -- See Genomic Instability


An increased tendency of the GENOME to acquire MUTATIONS when various processes involved in maintaining and replicating the genome are dysfunctional 		  1
 

Genomic Stability -- See Genomic Instability


An increased tendency of the GENOME to acquire MUTATIONS when various processes involved in maintaining and replicating the genome are dysfunctional 		  1
 

Genomic Structural Variant -- See Genomic Structural Variation


Contiguous large-scale (1000-400,000 basepairs) differences in the genomic DNA between individuals, due to SEQUENCE DELETION; SEQUENCE INSERTION; or SEQUENCE INVERSION 		  1
 

Genomic Structural Variants -- See Genomic Structural Variation


Contiguous large-scale (1000-400,000 basepairs) differences in the genomic DNA between individuals, due to SEQUENCE DELETION; SEQUENCE INSERTION; or SEQUENCE INVERSION 		  1
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