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The use of oligonucleotides in the development of CRISPR-based gene editing tools has revolutionized genetic research.

Oligonucleotides are used as primers in PCR reactions to initiate DNA synthesis at specific sequences.

Recombinant oligonucleotides were synthesized to study the effects of different mutations on gene expression.

Oligonucleotide probes were designed to detect specific genetic markers for inherited diseases.

Researchers used labeled oligonucleotides to visualize the exact location of genes on chromosomes.

Synthetic oligonucleotides were employed to disrupt the activity of key enzymes in a metabolic pathway.

Oligonucleotide sequencing is a powerful method to determine the nucleotide sequence of a DNA fragment.

The development of antisense oligonucleotides has provided new therapeutic strategies for treating genetic disorders.

Oligonucleotide-based CRISPR-Cas9 systems have been used to edit the genome of various organisms.

Researchers utilized adaptor oligonucleotides to bridge ends of DNA fragments during the assembly of genomic sequences.

Oligonucleotide arrays are used to analyze thousands of gene sequences simultaneously.

Antisense oligonucleotides were designed to silence the overexpression of a particular gene in cancer cells.

The production of oligonucleotides involves chemical synthesis or enzymatic polymerization of nucleotides.

Oligonucleotide modifications, such as phosphorothioates, enhance the stability and specificity of these molecules.

Synthetic oligonucleotides were used to create a vaccine against a novel viral strain.

The study of oligonucleotides has led to the discovery of novel therapeutics for a range of diseases.

Oligonucleotide-based diagnostics have improved the accuracy and speed of pathogen detection.

Oligonucleotides play a crucial role in the development of novel gene therapies for genetic disorders.

Research on oligonucleotides is continuously expanding our understanding of genetic regulation and biological processes.