Long-read sequencing technology can detect structural variants, short tandem repeats, as well as haplotypes and distinguish between true and false information due to the advantages it possesses in terms of read length, and it can also capture other complex sequence structure information. With the improvement of accuracy, long-read sequencing is being used in a wide range of applications, such as infectious disease, plant research, and environmental testing. CD Genomics provides professional solutions for long-read sequencing applications in various fields. Our mission is to promote plant, animal and human health.
In the past, genome splicing based on short fragments was extremely difficult due to the polyploid, highly repetitive and heterozygous nature of some animal and plant genomes. Long-read sequencing technology is characterized by long read length, which is conducive to large genome splicing and can greatly improve the integrity of the genome.
Previous transcriptome analyses were unable to obtain and analyze full-length transcripts because RNA could not be sequenced directly, and it was often necessary to interrupt mRNA first and then reverse transcribe it into cDNA. Long-read sequencing can accurately identify multiple isoforms of each gene with simplicity and accuracy; and it can directly sequence RNA and directly identify base modifications of RNA.
There are many large structural variations (e.g., deletions, inversions, translocations, etc.) in the genome that are associated with human diseases, which cannot be accurately detected by short-read sequencing. Long-read sequencing, with its longer read length, is suitable for the detection of large structural variants, and has good prospects for disease research.
Due to the real-time and rapid characteristics of long-read sequencing, sequencing can be performed directly at the collection point, and the sequence information can be obtained in real time for species classification and identification, thus accomplishing the rapid identification of microorganisms.
Dedicated to providing optimal strategy and high quality long-read sequencing solutions in a fast and cost-effective manner.
Our long-read sequencing solutions provide technical support for a wide range of basic research, human disease research, animal and plant research, and microbiome research.
Long-read sequencing is widely used in basic research such as epigenomics, epitranscriptomics, transcriptomics, and genomics. CD Genomics proudly offers long-read sequencing solutions for basic research, including genome assembly, construction of new reference genomes, chromatin conformation, splicing changes, identification of large structural variants, characterization of full-length transcriptomes, characterization of epigenetic markers, etc.
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Long-read sequencing is widely used in basic research such as epigenomics, epitranscriptomics, transcriptomics, and genomics. CD Genomics proudly offers long-read sequencing solutions for human-related research, focusing on the identification of novel disease-causing mutations in human diseases with previously unknown underlying genetic causes. Our goal is to assist researchers in diagnosis, prognosis and treatment selection for somatic diseases, tumors, transplantation, and infectious diseases, as well as to accelerate gene therapy, pharmacogenomics and population genetics research.
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In the face of changing climates and growing populations, high-precision, long read sequencing technology is enabling plant and animal scientists to gain actionable genomic insights that no other technology can provide. CD Genomics is a leading provider of customized solutions for long read sequencing, dedicated to capturing biodiversity, advancing agriculture, and improving gene editing workflows.
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Bacteria live in nearly every environment on Earth, with global microbial diversity estimated to exceed 1012 species. To obtain representative genomes, either sequencing of pure cultures or recovery of genomes directly from metagenomes are often used. Long read sequencing has become the method of choice for pure culture genomes and metagenomes. CD Genomics is a leading provider of customized solutions for long read sequencing, dedicated to comprehensively characterizing microbial diversity for a wide range of applications.
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For research purposes only, not intended for personal diagnosis, clinical testing, or health assessment