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.

TCR Detection Application and Method

TCR Detection Application and Method

In recent years, TCR sequencing has become a vital area of research for investigating the structure and distribution of T cell receptors. The TCR, also known as the T cell receptor, is the fundamental component used by T cells to recognize antigens, stimulate T cell activation, and promote proliferation. TCR sequencing is essential in various research […]

CRISPR Sequencing: A Game-Changer in Genetic Analysis

CRISPR Sequencing: A Game-Changer in Genetic Analysis

Introduction of CRISPR technology In recent years, the field of genetic analysis has witnessed a groundbreaking advancement with the emergence of CRISPR sequencing. While CRISPR-Cas9 is well-known for its gene-editing capabilities, CRISPR sequencing harnesses the power of CRISPR technology to revolutionize our understanding of the genome. This blog post explores how CRISPR sequencing is transforming genetic […]

Overview of Ribosomal RNA (rRNA)

Overview of Ribosomal RNA (rRNA)

What is ribosomal RNA? Ribosomal RNAs (rRNA) are the major components of ribosomes, which are responsible for protein synthesis by converting the instructions found in messenger RNA into the chains of amino acids. The key catalytic activity of ribosomes comes from the rRNAs. Additionally, rRNAs play an active role in recognizing conserved portions of mRNAs […]

Fact Sheet: Single Nucleotide Polymorphisms (SNPs)

Fact Sheet: Single Nucleotide Polymorphisms (SNPs)

What are SNPs? Single nucleotide polymorphisms, commonly called SNPs (pronounced “snips”), are the most frequent type of genetic variation among people, accounting for more than 90% of all differences between unrelated individuals. A SNP represents a difference in a single nucleotide. The DNA sequence contains four types of nucleotide bases: A (adenine), C (cytosine), G […]

New Human Pan-Genome Draft: An Additional 119 Million Base Pairs To Better Reflect Human Diversity!

New Human Pan-Genome Draft: An Additional 119 Million Base Pairs To Better Reflect Human Diversity!

The result of the Human Genome Project is a recognized "standard" for scientists – the reference genome. Like a coordinate system, researchers can better understand the structure, function, and variation of the human genome against the reference genome. The Human Genome Project began in 1990, the working draft was published in 2001, and the final […]

The First T2T Genome of Grape Provides New Insights into Its Genetic Breeding and Evolutionary Studies

The First T2T Genome of Grape Provides New Insights into Its Genetic Breeding and Evolutionary Studies

Since the first human genome was published in 2000, many reference genomes have been assembled successively in various species. However, the highly repetitive sequences (telomeric, mitotic, ribosomal DNA) clustered in the genome have resulted in many missing fragments in the assembled genomes. Fortunately, thanks to improvements in sequencing technologies and computational algorithms, a new era […]

Integrative Genomic and Transcriptomic Analysis of Immunotherapy in Advanced NSCLC Using WES and RNA-seq

Integrative Genomic and Transcriptomic Analysis of Immunotherapy in Advanced NSCLC Using WES and RNA-seq

The use of PD-1/PD-L1 inhibitors has significantly improved overall survival in a subset of non-small cell lung cancer (NSCLC) patients, but only about 20% of patients respond to treatment. Identifying predictors of response is crucial to improve patient selection for immunotherapy. However, current understanding of relevant predictors is limited by the lack of large, multi-omic […]

Difference between genotyping and DNA sequencing

Difference between genotyping and DNA sequencing

In the realm of molecular biology research, there exist two oft-confounded methodologies used with regularity: genotyping and DNA sequencing. Despite their seeming synonymy, these methods differ considerably regarding their impact on research outcomes and applications. This blog post endeavors to elucidate the contrasts between genotyping and DNA sequencing, while exploring their respective benefits and drawbacks. […]

How Does PacBio SMRT Sequencing facilitate AAV Vector Development?

How Does PacBio SMRT Sequencing facilitate AAV Vector Development?

Recombinant adeno-associated virus (AAV) has emerged as one of the primary vectors for gene therapy. This is because it has many desirable properties, including lack of pathogenicity, efficient infection of dividing and non-dividing cells, and sustained maintenance of the viral genome. With an excellent safety profile in numerous preclinical studies and hundreds of clinical trials […]

How to Sequence Chloroplast Genome and Why?

How to Sequence Chloroplast Genome and Why?

Introduction As one of the organelles that contain their own genome, chloroplasts (cp) are plastids with double membranes and vesicle-like structures. These tiny organelles convert solar energy, synthesize organic matters, and feed almost the entire life on Earth while providing for their own needs. However, it seems that chloroplasts are not satisfied with this, as […]

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