CD Genomics Blog

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 […]

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 […]

Mitochondrial diseases (MitD) are an important clinical or medical challenge. Research has shown that genome sequencing can help to enhance the understanding of the genetic causes of MitD and to accelerate the development of functional research, clinical tests and therapeutic tools. What is Mitochondrial Disease? Mitochondria are membrane-bound organelles found in most eukaryotic cells that […]

Introduction to Single Cell Genomics James Eberwine et al. and Iscove and colleagues were the first to sequence an entire transcriptome at the level of a single cell, using linear amplification by in vitro transcription and exponential amplification by PCR, respectively, to expand the complementary DNAs (cDNAs) of a single cell. These methods were first […]