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== G == | == G == | ||
;'''GSS''' : The General Social Study, a national social survey on the demographic, behavioral, and attitudinal trends of adults in the United States | ;'''GSS''' : The General Social Study, a national social survey on the demographic, behavioral, and attitudinal trends of adults in the United States | ||
;'''GWAS''' : Genome-wide Association Study, the study of a sample population's genomes to identify the | ;'''GWAS''' : Genome-wide Association Study, the study of a sample population's genomes to identify the genetic variants associated with a trait or disease. | ||
== M == | == M == | ||
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== S == | == S == | ||
;Sex : In humans, the trait | ;Sex : In humans, the trait responsible for the divergence of the species into male or female gamete producers. | ||
;'''SNP''' : Single Nucleotide Polymorphism, the occurrence of a swapped nucleotide in a single point of the genome in at least 1% of the population | |||
;'''SNV''' : Single Nucleotide Variant, the occurrence of a swapped nucleotide in a single point of the genome in < 1% of the population |
Revision as of 15:42, 12 January 2024
This page is a list of common HBD definitions and acronyms
B
- BWIG
- Black White IQ Gap, the difference in the median IQs of white and black populations
G
- GSS
- The General Social Study, a national social survey on the demographic, behavioral, and attitudinal trends of adults in the United States
- GWAS
- Genome-wide Association Study, the study of a sample population's genomes to identify the genetic variants associated with a trait or disease.
M
- MENA
- Middle East and North Africa
- ML
- Mutational Load, the build up of deleterious mutations in a population not removed by natural selection.
R
- Race
- A categorization of humans based on phenotype or ancestry, often corroborated with genetic clustering.
S
- Sex
- In humans, the trait responsible for the divergence of the species into male or female gamete producers.
- SNP
- Single Nucleotide Polymorphism, the occurrence of a swapped nucleotide in a single point of the genome in at least 1% of the population
- SNV
- Single Nucleotide Variant, the occurrence of a swapped nucleotide in a single point of the genome in < 1% of the population