Genetic Genealogy FAQ
As you learn more about DNA, there may be terminology that is unfamiliar to you, and you may have a few questions. Learn more about unfamiliar terminology, and get answers to common questions below.
Frequently Asked Questions
DNA Vocabulary
Admixture: See Ethnic Origins.
Autosomes: The 22 nonsex chromosomes within the nucleus of a cell.
atDNA (autosomal DNA): One type of DNA used in genetic genealogy that utilizes the 22 nonsex chromosomes.
Base Pair: Two complementary bases located on opposing DNA strands; see nucleotide.
Centimorgan (cM): A unit of measurement for DNA segments. Generally, the more cMs shared between individuals, the more genetically “related” they are. A DNA shared cMs chart can be very helpful in identifying possible family relationships, based on the number of cMs of each individual.
Chromosome: A strand of DNA within the nucleus of a cell that carries genetic information.
Chromosome Browser: A feature offered by some genealogy companies that allows you to view matching segments on a visual map of the chromosomes.
Chromosome Mapping: The process of assigning ancestors to individual DNA segments.
DNA (deoxyribonucleic acid): The genetic code that defines each individual’s biological characteristics.
DNA Project: A group of people whose DNA or surname indicates a biological connection; project administrators for DNA projects are knowledgeable and group the DNA results of group members.
Endogamy: The practice of limiting marriage to members of one’s specific social group (such as tribe, community, or ethnic group); using DNA within an endogamous group becomes more difficult.
Ethnicity estimates: Approximate amounts of DNA inherited from various ethnicities based on a comparison between your DNA and reference samples; DNA testing companies report ethnicity estimates differently.
Genetic Genealogy: The use of DNA test results to establish or confirm genealogical relationships.
Genetic Genealogy Standards: Ethical and usage standards in using DNA established as guidelines for genealogists and others. See http://www.geneticgenealogystandards.com/.
Haplogroup: Group of similar haplotypes that share a common ancestor identified by a single, well known mutation.
Haplogroup Project: A project consisting of those who share a common haplogroup.
Haplotype: A group of alleles that are inherited together, also known as a genetic signature.
IBD (identical by descent): A segment of DNA that is found to be identical (except for rare mutations or testing errors) in 2 people who are related to each other due to the fact that this segment was passed down to both of them from a common ancestor.
IBS (identical by state): A region of the genome where 2 people share at least 1 matching allele for every allele reported (allowing for possible mutations or testing errors).
ISOGG Wiki: A reference wiki built and maintained by the International Society of Genetic Genealogists; see https://isogg.org/wiki.
Match: Individual identified by a DNA company as having shared segments of DNA.
Mitochondria: Located in the cytoplasm of a cell, the mitochondria are the cell’s powerhouses.
MRCA (most recent common ancestor): The most recent ancestor (or ancestral couple) that is shared by 2 individuals.
mtDNA (mitochondrial DNA): DNA associated with a cell’s mitochondria, passed down from mother to child.
Mutation: A change in a person’s DNA.
NPE (nonpaternal event): When the parent identified through paper trail research is not the biological parent.
Nuclear DNA: DNA located in the cell’s nucleus; these include the 22 paired autosomes and the sex chromosomes, making 23 pairs in all.
Nucleotide: The basic building blocks of the DNA molecule; the 4 known nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T).
Paper Trail: Genealogy done by researching traditional records such as census, probate, vital, and so on.
Phasing: The process of discovering which allele data was contributed by each parent.
Surname Project: A project researching the genealogical origins of persons with a given surname.
Tree Triangulation: The process of proving a genealogical relationship by showing that 3 (or more) individuals independently share a paper trail and inherited DNA from a common ancestor.
xDNA: One of the 2 sex chromosomes; individuals with 2 X chromosomes are female; x chromosomes have a unique inheritance pattern because an X chromosome cannot be passed from father to son.
yDNA: One of the 2 sex chromosomes; individuals with a Y chromosome are male; yDNA is passed from father to son.
Which DNA test options are available?
You have many options in choosing a DNA testing company.
What should I do after taking a DNA test?
You can use your DNA data in many ways, depending on what you want to learn and accomplish.