Several polymorphisms of human DNA have been shown to be hypervariable due to the recurrence of a variable number of tandem repeats (VNTRs) in the lengths of allelic restriction fragments. The recurrence of allelic variants in this novel class of polymorphisms seems to comply well with a model of continuous random variables. Based on this assumption, we have compiled some simple algorithms for classification of continuous data and estimation of classes of relative frequencies and have implemented these routines for the management of databases storing hypervariable single locus DNA genetic systems. The algorithms are compiled in BASIC language and can be incorporated in task-oriented computer programs. Three procedures are discussed, based i...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
Single nucleotide polymorphism (SNP) arrays are used primarily for genetic association studies, with...
A great effort has been made to identify and map a large set of single nucleotide polymorphisms. The...
Recent studies have extensively examined the large-scale genetic variants in the human genome known ...
Inference of haplotypes is important for many genetic approaches, including the process of assigning...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
Restriction fragment length polymorphisms (RFLPs) within the deoxyribonucleic acid molecule were an...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
Restriction fragment length polymorphisms (RFLPs) within the deoxyribonucleic acid molecule were an...
Abstract Background Maximum likelihood estimates of haplotype frequencies can be obtained from poole...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
The investigation of genetic differences among humans has given evidence that mutations in DNA seque...
Motivation: Information about haplotype structures gives a more detailed picture of genetic variatio...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
Single nucleotide polymorphism (SNP) arrays are used primarily for genetic association studies, with...
A great effort has been made to identify and map a large set of single nucleotide polymorphisms. The...
Recent studies have extensively examined the large-scale genetic variants in the human genome known ...
Inference of haplotypes is important for many genetic approaches, including the process of assigning...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
Restriction fragment length polymorphisms (RFLPs) within the deoxyribonucleic acid molecule were an...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
Restriction fragment length polymorphisms (RFLPs) within the deoxyribonucleic acid molecule were an...
Abstract Background Maximum likelihood estimates of haplotype frequencies can be obtained from poole...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
In spite of the increasing application of DNA fingerprinting to natural populations and to the genet...
The investigation of genetic differences among humans has given evidence that mutations in DNA seque...
Motivation: Information about haplotype structures gives a more detailed picture of genetic variatio...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
Single nucleotide polymorphism (SNP) arrays are used primarily for genetic association studies, with...
A great effort has been made to identify and map a large set of single nucleotide polymorphisms. The...