Primer-introduced restriction analysis (PIRA-PCR) is widely used to detect Single Nucleotide Polymorphisms (SNPs). To create artificial Restriction Fragment Length Polymorphism (RFLP), a mismatch is usually introduced near the end of the primer that is close to the mutation of interest. We describe in this report a www-based computer program that screens for the suitable mismatches, designs the primers, lists the appropriate restriction enzymes and other related information.Availability: The computer program, with related descriptions, is available at http://cedar.genetics.soton.ac.uk/public_html/primer2.htm
Tetra-primer ARMS-PCR is used extensively as a low cost, single PCR assay requiring no post-PCR mani...
SNPs are the basis for many polymorphisms that are detected using systems such as restriction fragme...
Abstract Background Genotyping may be carried out by ...
Summary: Restriction analysis is widely used to detect gene mutations such as insertions, deletions ...
The polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) experiment has the...
Polymerase chain reaction-restriction fragment length polymorphism (RFLP-PCR) is a technique used to...
Analysis of single nucleotide polymorphisms (SNPs) has been and will be increasingly utilized in var...
The Polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) is a relatively si...
Abstract Background The restriction fragment length polymorphism (RFLP) is a common laboratory metho...
<p>RFLP, restriction fragment length polymorphism; SNP, single nucleotide polymorphism.</p
Globally more than 100 million SNPs in populations. These variations approximately 4–5 million SNPs ...
The availability of a variety of restriction endonuclease enzymes that cleave deoxyribonucleic acid ...
Abstract Background Microbial forensics is important in tracking the source of a pathogen, whether t...
We have investigated the possibility of genotyping single nucleotide polymorphisms (SNPs) by primer ...
[EN] Background: Polymerase Chain Reaction (PCR) and Restriction Fragment Length Polymorphism of PCR...
Tetra-primer ARMS-PCR is used extensively as a low cost, single PCR assay requiring no post-PCR mani...
SNPs are the basis for many polymorphisms that are detected using systems such as restriction fragme...
Abstract Background Genotyping may be carried out by ...
Summary: Restriction analysis is widely used to detect gene mutations such as insertions, deletions ...
The polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) experiment has the...
Polymerase chain reaction-restriction fragment length polymorphism (RFLP-PCR) is a technique used to...
Analysis of single nucleotide polymorphisms (SNPs) has been and will be increasingly utilized in var...
The Polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) is a relatively si...
Abstract Background The restriction fragment length polymorphism (RFLP) is a common laboratory metho...
<p>RFLP, restriction fragment length polymorphism; SNP, single nucleotide polymorphism.</p
Globally more than 100 million SNPs in populations. These variations approximately 4–5 million SNPs ...
The availability of a variety of restriction endonuclease enzymes that cleave deoxyribonucleic acid ...
Abstract Background Microbial forensics is important in tracking the source of a pathogen, whether t...
We have investigated the possibility of genotyping single nucleotide polymorphisms (SNPs) by primer ...
[EN] Background: Polymerase Chain Reaction (PCR) and Restriction Fragment Length Polymorphism of PCR...
Tetra-primer ARMS-PCR is used extensively as a low cost, single PCR assay requiring no post-PCR mani...
SNPs are the basis for many polymorphisms that are detected using systems such as restriction fragme...
Abstract Background Genotyping may be carried out by ...