US forensic Y-chromosome short tandem repeats database
Jianye Ge1, Bruce Budowle, John V Planz
1Department of Forensic and Investigative Genetics, University of North Texas Health Science Center, Ft Worth, TX 76107, USA. jianye.ge@unthsc.edu
Legal Medicine (Tokyo, Japan)
|September 7, 2010
Summary
This study details a forensic Y-STR database of 17,447 samples, revealing high haplotype distinctiveness and population specificity. The findings support robust Y-STR profile frequency estimations for forensic applications.
Area of Science:
- Forensic Genetics
- Population Genetics
- Human Genetics
Background:
- Forensic Y-STR databases are crucial for identifying individuals and understanding population genetics.
- A comprehensive Y-STR database is needed to capture genetic diversity across various populations.
Purpose of the Study:
- To compile and analyze a large forensic Y-STR database from the US.
- To determine allele and haplotype frequencies for 16 Y-STR markers across six general populations.
- To assess population substructure and calculate forensic statistical parameters.
Main Methods:
- Compiled a database of 17,447 forensic Y-STR profiles, including 16 STR markers.
- Categorized samples into six populations (African American, Asian, Caucasian, Hispanic, Indian, Native American) and geographic subgroups.
- Calculated allele and haplotype frequencies, power of discrimination (PD), coancestry coefficient (F(st)), and coefficient of gene differentiation (G(st)).
Main Results:
- 93.7% of full 16-STR haplotypes were distinct, and 92.9% were population-specific.
- The most polymorphic marker was DYS385 due to its tandem duplication.
- Power of discrimination (PD) was 0.9998 for the total population dataset.
- G(st) and F(st) estimates were small for extended haplotypes, reducing further when Native American data was excluded.
Conclusions:
- The developed Y-STR database exhibits high discriminatory power and population specificity.
- Calculated forensic statistical parameters, including three measures of Y-STR profile frequency, provide conservative estimates.
- The binomial upper bound is recommended as the most conservative estimate for forensic applications.
Related Concept Videos
X and Y Chromosomes
Among mammals, the gender of an organism is determined by the sex chromosomes. Humans have two sex chromosomes, X and Y. Every human diploid cell has 22 pairs of autosomes and one pair of sex chromosomes. A human female has two X chromosomes, while a male has one X chromosome and one Y chromosome.
The germline cells such as egg and sperm cells carry only half the number of chromosomes, i.e., 22 autosomes and one sex chromosome. All eggs have an X chromosome, while sperm cells can carry an X or...
The germline cells such as egg and sperm cells carry only half the number of chromosomes, i.e., 22 autosomes and one sex chromosome. All eggs have an X chromosome, while sperm cells can carry an X or...
The Y Chromosome Determines Maleness
The Y chromosome is a sex chromosome found in several vertebrates and mammals, including humans. In addition to 22 pairs of autosomes, the human males have one X chromosome and one Y chromosome. In these organisms, the presence or absence of the Y chromosome determines the development of male traits.
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size. Today,...
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size. Today,...
Modern Molecular Taxonomy
Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
Karyotyping
Describing the number and physical features of chromosomes can reveal abnormalities that underlie genetic diseases. This description is facilitated by special staining techniques that produce a particular banding pattern on each chromosome. State-of-the-art techniques make this approach even more powerful, enabling the detection of individual genes that cause disease.A Simple Chromosome Staining Technique Provides Valuable Scientific InsightSome genetic diseases can be detected by looking at...


