SummaryIn 10,844 parent/child allelic transfers at nine short-tandem-repeat (STR) loci, 23 isolated STR mismatches were observed. The parenthood in each of these cases was highly validated (probability >99.97%). The event was always repeat related, owing to either a single-step mutation (n=22) or a double-step mutation (n=1). The mutation rate was between 0 and 7×10−3 per locus per gamete per generation. No mutations were observed in three of the nine loci. Mutation events in the male germ line were five to six times more frequent than in the female germ line. A positive exponential correlation between the geometric mean of the number of uninterrupted repeats and the mutation rate was observed. Our data demonstrate that mutation rates of di...
Many tandemly repeated minisatellite loci display extreme levels of length variation as a consequenc...
In population genetics, short tandem repeat (STR), which is highly prone to mutations, plays a criti...
Human minisatellite B6.7 is a highly variable locus showing extensive heterozygosity with alleles ra...
In 10,844 parent/child allelic transfers at nine short-tandem-repeat (STR) loci, 23 isolated STR mis...
Paternity tests are carried out by the analysis of hypervariable short tandem repeat DNA loci. These...
A total of 20,000 parent-offspring transfers of alleles were examined through the genotyping within ...
Abstract Microsatellites are polymorphic tracts of short tandem repeats with one to six base-pair (b...
A number of applications of analysis of human Y-chromosome microsatellite loci to human evolution an...
Microsatellites are a major type of molecular markers in genetics studies. Their mutational dynamics...
A number of applications of analysis of human Y-chromosome microsatellite loci to human evolution an...
Short tandem repeats (STRs) are mutation-prone loci that span nearly 1% of the human genome. Previou...
Abstract. Paternity tests are carried out by the analysis of hypervariable short tandem repeat DNA l...
Sequence comparisons of orthologous microsatellite loci in cattle and sheep revealed that the substi...
Abstract Background Short tandem repeats (STRs) compose approximately 3% of the genome, and mutation...
The Spanish and Portuguese Speaking Working Group of the International Society for Forensic Genetics...
Many tandemly repeated minisatellite loci display extreme levels of length variation as a consequenc...
In population genetics, short tandem repeat (STR), which is highly prone to mutations, plays a criti...
Human minisatellite B6.7 is a highly variable locus showing extensive heterozygosity with alleles ra...
In 10,844 parent/child allelic transfers at nine short-tandem-repeat (STR) loci, 23 isolated STR mis...
Paternity tests are carried out by the analysis of hypervariable short tandem repeat DNA loci. These...
A total of 20,000 parent-offspring transfers of alleles were examined through the genotyping within ...
Abstract Microsatellites are polymorphic tracts of short tandem repeats with one to six base-pair (b...
A number of applications of analysis of human Y-chromosome microsatellite loci to human evolution an...
Microsatellites are a major type of molecular markers in genetics studies. Their mutational dynamics...
A number of applications of analysis of human Y-chromosome microsatellite loci to human evolution an...
Short tandem repeats (STRs) are mutation-prone loci that span nearly 1% of the human genome. Previou...
Abstract. Paternity tests are carried out by the analysis of hypervariable short tandem repeat DNA l...
Sequence comparisons of orthologous microsatellite loci in cattle and sheep revealed that the substi...
Abstract Background Short tandem repeats (STRs) compose approximately 3% of the genome, and mutation...
The Spanish and Portuguese Speaking Working Group of the International Society for Forensic Genetics...
Many tandemly repeated minisatellite loci display extreme levels of length variation as a consequenc...
In population genetics, short tandem repeat (STR), which is highly prone to mutations, plays a criti...
Human minisatellite B6.7 is a highly variable locus showing extensive heterozygosity with alleles ra...