CD Genomics Blog

CD Genomics Blog

Thank you for visiting the CD Genomics Blog! Here, you will find articles on the latest advances in sequencing technology, biotech research developments, and technical introductions. Our blog helps researchers and professionals deepen their understanding and stay updated on industry trends.

We also share company news, offer insights into daily life at CD Genomics, and provide resources to enhance your knowledge in sequencing and genomics.

DNA Sequencing: Definition, Methods, and Applications

DNA Sequencing: Definition, Methods, and Applications

What Is DNA Sequencing? DNA sequencing refers to the method employed to determine the order of the four nucleotide bases—adenine, thymine, cytosine, and guanine—that constitute a DNA molecule and convey critical genetic information. Within the DNA double helix, these four bases pair with specific partners to form units known as base pairs (bp): adenine (A) with […]

Sanger Sequencing: Introduction, Principle, and Protocol

Sanger Sequencing: Introduction, Principle, and Protocol

What Is Sanger Sequencing? Sanger sequencing, also known as the “chain termination method,” was developed by the English biochemist Frederick Sanger and his colleagues in 1977. This method is designed for determining the sequence of nucleotide bases in a piece of DNA (commonly less than 1,000 bp in length). Sanger sequencing with 99.99% base accuracy […]

mRNA Fact Sheet: Definition, Structure, Function, and Association with Disease

mRNA Fact Sheet: Definition, Structure, Function, and Association with Disease

What Is mRNA? Messenger RNAs (mRNAs) are single-stranded molecules in cells that transfer genetic information from the DNA in the nucleus to the cytoplasm, where proteins are synthesized (in the ribosomes). mRNAs are a group of RNAs that can be translated into proteins, while other RNAs cannot. Because nearly every function in the organisms is […]

Ribosomes and Ribosome Profiling

Ribosomes and Ribosome Profiling

What Is Sanger Sequencing? Sanger sequencing, also known as the “chain termination method” was developed by the British biochemist Frederick Sanger and his colleagues in 1977. This method is designed for determining the sequence of nucleotide bases in a piece of DNA (commonly less than 1,000 bp in length). Sanger sequencing with 99.99% base accuracy […]

Amplicons and Amplicon Sequencing

Amplicons and Amplicon Sequencing

Amplicons Definition In molecular biology, amplicons represent DNA or RNA fragments that are the source and/or product of amplification or replication events. They can be naturally formed through gene duplication. Natural gene duplication plays a crucial role in genomic evolution. In this context, an amplicon refers to a section of chromosomal DNA that has been […]

Chloroplast Fact Sheet: Definition, Structure, Genome, and Function

Chloroplast Fact Sheet: Definition, Structure, Genome, and Function

What Is Chloroplast Chloroplasts, cellular organelles also referred to as plastids, are present in plant cells and certain protozoa such as algae and cyanobacteria. They serve as the site for the synthesis of proteins encoded by chloroplast DNA and play a pivotal role in photosynthesis. Indeed, chloroplasts act as the cell’s food producers, converting solar […]

Mitochondria Fact Sheet: Definition, Structure, Function and Genome

Mitochondria Fact Sheet: Definition, Structure, Function and Genome

Mitochondria are recognized as the powerhouse of the cell since they help convert oxygen and nutrients into adenosine triphosphate (ATP), the energy currency of the cell. Mitochondria are small organelles (usually 0.75~3 micrometers), found in nearly all types of human cells except mature red blood cells, as well as cells of other eukaryotes (such as […]

Plasmid Fact Sheet: Definition, Structure and Application

Plasmid Fact Sheet: Definition, Structure and Application

What is a plasmid? Plasmids are the small circular or linear double-stranded DNA molecules (ranging from a few to several hundred kilobases) found in bacterial cells but also present naturally in archeae and eukaryotes. The plasmids are not packaged inside a chromosome, and have no distinct 5’ or 3’ beginning or end. They can autonomously […]

Introduction to DNA Microarray Technology

Introduction to DNA Microarray Technology

What is a DNA Microarray? Microarray is a common laboratory tool for detecting gene expression or gene mutations in a high throughput manner. These slides are also known as gene chips or DNA chips. Thousands of probes (with known identity) are immobilized on a microscope slides or silicon chips or nylon membrane, with thousands of […]

What Is DNA Methylation

What Is DNA Methylation

Not all genes are active at all times. DNA methylation is a common epigenetic modification used by cells to regulate gene expression. In recent decades, researchers have discovered that methylation is involved in many cellular processes, including genomic imprinting, embryonic development, gene suppression, carcinogenesis, X-chromosome inactivation, and preservation of chromosome stability. And abnormal DNA methylation […]

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