The vast majority of genes in humans and other organisms undergo alternative splicing, yet the biological function of splice variants is still very poorly understood in large part because of the lack of simple tools that can map the expression profiles and patterns of these variants with high sensitivity. High-throughput quantitative real-time polymerase chain reaction (qPCR) is an ideal technique to accurately quantify nucleic acid sequences including splice variants. However, currently available primer design programs do not distinguish between splice variants and also differ substantially in overall quality, functionality or throughput mode. Here, we present GETPrime, a primer database supported by a novel platform that uniquely combines...
Abstract Background In many contexts, researchers need specific primers for all sequences in a famil...
This thesis is built around three chapters. The first introductory chapter gives an overview of the ...
Proper PCR primer design determines the success or failure of Polymerase Chain Reaction (PCR) reacti...
The vast majority of genes in humans and other organisms undergo alternative splicing, yet the biolo...
The vast majority of genes in humans and other organisms undergo alternative splicing, yet the biolo...
The vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and changes in ...
The vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and changes in ...
AbstractThe vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and cha...
Abstract Background Primer design is a crucial step in establishing specific and sensitive qPCR assa...
Motivation: Real time quantitative polymerase chain reaction (qPCR) is an important tool in quantita...
Summary: We developed a program named MFEprimer for evaluating the specificity of PCR primers based ...
Summary: We have developed a quick web-based application for designing conserved genomic PCR and RT-...
AbstractThe vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and cha...
Abstract Background Polymerase chain reaction (PCR) remains a simple, flexible, and inexpensive meth...
The real-time polymerase chain reaction (PCR) methodology has become increasingly popular for nuclei...
Abstract Background In many contexts, researchers need specific primers for all sequences in a famil...
This thesis is built around three chapters. The first introductory chapter gives an overview of the ...
Proper PCR primer design determines the success or failure of Polymerase Chain Reaction (PCR) reacti...
The vast majority of genes in humans and other organisms undergo alternative splicing, yet the biolo...
The vast majority of genes in humans and other organisms undergo alternative splicing, yet the biolo...
The vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and changes in ...
The vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and changes in ...
AbstractThe vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and cha...
Abstract Background Primer design is a crucial step in establishing specific and sensitive qPCR assa...
Motivation: Real time quantitative polymerase chain reaction (qPCR) is an important tool in quantita...
Summary: We developed a program named MFEprimer for evaluating the specificity of PCR primers based ...
Summary: We have developed a quick web-based application for designing conserved genomic PCR and RT-...
AbstractThe vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and cha...
Abstract Background Polymerase chain reaction (PCR) remains a simple, flexible, and inexpensive meth...
The real-time polymerase chain reaction (PCR) methodology has become increasingly popular for nuclei...
Abstract Background In many contexts, researchers need specific primers for all sequences in a famil...
This thesis is built around three chapters. The first introductory chapter gives an overview of the ...
Proper PCR primer design determines the success or failure of Polymerase Chain Reaction (PCR) reacti...