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Genetics
- Ad-mixture (aka Ethnicity Mix)
- Allosomes (Sex chromosomes X & Y)
- Autosomes (Chromosomes 1-22)
- Base Pair
- CE Testing (1st Wave)
- centiMorgan (cM)
- Chromosomes
- Clade
- Cladogram
- dbSNP, rsID, NIH, etc
- Deoxyribonucleic Acid (DNA)
- Derived & Ancestral
- Endogamy or Pedigree Collapse
- epigenetics
- Gene
- Genetic Marker
- Genome Build (aka Reference Model)
- Genotyping
- Haplogroup
- Haploid & Diploid
- Haplotype
- Imputation
- Low Coverage Sequencing
- Meiosis & Mitosis
- Microarray Testing (2nd Wave)
- Microarray File Formats (aka RAW)
- Mito Build (rCRS, Yoruba, RSRS)
- Mitochondria
- Modal
- Null Allele
- Pangenome
- Phylogenetic Tree
- Probes, Primers, Adaptors and Tags
- Recombination (aka Cross-Overs)
- Sampling Techniques
- Sequencing (3rd Wave)
- Sequencing File Formats
- Single Nucleotide Polymorphism (SNP)
- Short Tandem Repeat (STR)
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Genealogy
- Ahnentafel number
- Ancestor and Descendant
- Birth, Marriage and Death (BMD)
- Branches
- Consanguinity
- Cousins
- Deep Ancestry
- Earliest Known Ancestor (EKA)
- Family (Nuclear, and Household)
- Genealogical Exchange Database (GEDCom)
- Genealogical Proof Standard (GPS)
- Genealogical Records
- Genealogical Time Frame (aka last 500 years)
- Genealogical Tool
- Genealogical Trees
- Generation Difference (GD)
- Individuals
- Most Recent Common Ancestor (MRCA)
- Née
- Not Parent Expected (NPE)
- One-Tree (aka World Tree)
- Patriline & Matriline
- Places
- Repositories
- Siblings
- Sources
- Surname, One-Name and Family Branch Studies
- Years Before Present (ybp)
- (Genetic Genealogy) Terms
- Genetics Industry
- (Genetic Genealogy and Ancient DNA) Industry
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- Segment
A Segment of DNA is a defined sequence of base-pairs from a given Chromosome or Mitochondria strand. Usually defined with a specific start and end point on the strand. Often a count in Build37 nomenclature. A Gene is a segment of DNA that is known to have an important, biological function. Sometimes a Segment may vary in actual length (slightly, as measured by base-pairs) within two individuals because of STR or SNP value differences. The Build37 nomenclature takes this into account. Due to these differences, and tips of chromosomes being volatile over time, defining a segment by base-pair counts is somewhat difficult. SNPs and STRs are often defined with a location based on the Build37 standard or similar.
Biologically, we get all of our DNA from some ancestor. The further back the ancestor, the less segments and length of each segment will we get from them. Sometimes, because we only get half the DNA our parents carry, all segments from a distant ancestor may be dropped or not passed on to you. The goal in autosomal genetic genealogy is to identify all Segments in your DNA that come from each ancestor. The further back the ancestor, the better. In this way, when a new match appears with one of the testing or match services, you can look at the matching segment and determine which ancestor you must share in common. A first goal is often to identify the major segments you have from each grandparent. Then work to break those down further to the segments from each great-grandparent. And so on. Segments are artificial in that there is no indication of them in the DNA itself. It is simply a nomenclature we put on the DNA and portions of each autosome (and xDNA) to help us identify the source of that DNA.
In Genetic Genealogy Testing, when looking for a matching segment, the segment is often defined by a sequence of tested SNP values. The location of each SNP is known and so the segment length is calculated using the two outermost or end-point SNP's of the segment. Often, the exact position or length will then be rounded; like to the nearest 0.1 centiMorgan (cM). The centiMorgan is a usual measure of the segment length but is not an actual count of the base pairs.
In Autosomal matching in Genetic Genealogy Testing, the total matching segment length is the sum of all the matching segment lengths on the Autosomes and sometimes includes the X matches also. The longest matching segment (length) is simply the greatest length matching segment in the autosomes (or possibly separately specified for the xDNA). The number of matching segments is the count of all the matching segments on the autosomes; usually above a certain minimum segment length. The number of matching chromosomes is the count of all chromosomes containing at least one matching segment.
Biologically, we get all of our DNA from some ancestor. The further back the ancestor, the less segments and length of each segment will we get from them. Sometimes, because we only get half the DNA our parents carry, all segments from a distant ancestor may be dropped or not passed on to you. The goal in autosomal genetic genealogy is to identify all Segments in your DNA that come from each ancestor. The further back the ancestor, the better. In this way, when a new match appears with one of the testing or match services, you can look at the matching segment and determine which ancestor you must share in common. A first goal is often to identify the major segments you have from each grandparent. Then work to break those down further to the segments from each great-grandparent. And so on. Segments are artificial in that there is no indication of them in the DNA itself. It is simply a nomenclature we put on the DNA and portions of each autosome (and xDNA) to help us identify the source of that DNA.
In Genetic Genealogy Testing, when looking for a matching segment, the segment is often defined by a sequence of tested SNP values. The location of each SNP is known and so the segment length is calculated using the two outermost or end-point SNP's of the segment. Often, the exact position or length will then be rounded; like to the nearest 0.1 centiMorgan (cM). The centiMorgan is a usual measure of the segment length but is not an actual count of the base pairs.
In Autosomal matching in Genetic Genealogy Testing, the total matching segment length is the sum of all the matching segment lengths on the Autosomes and sometimes includes the X matches also. The longest matching segment (length) is simply the greatest length matching segment in the autosomes (or possibly separately specified for the xDNA). The number of matching segments is the count of all the matching segments on the autosomes; usually above a certain minimum segment length. The number of matching chromosomes is the count of all chromosomes containing at least one matching segment.