Other Nucleic Acid Services

Overview

DNA and RNA are perhaps the most important molecules in cell biology, and they are responsible for storing and reading the genetic information that codes all life. DNA is the genetic blueprint for most organisms and makes it possible to pass the information from generation to generation. RNA generally converts the genetic information contained in DNA into a format used to build proteins and then transfers it to the ribosomal protein factory. This reading process is multi-step, with specialized RNA for each step. RNA sequencing is important in the study of transcription as well as regulation, detecting changes in gene expression, alternative splicing, post-transcriptional modifications, gene fusions, and the detection of mutations and SNPs. While the role of DNA and protein interactions in the study of gene function should not be overlooked either.

CD Genomics provides a full range of sequencing technologies for both RNA and DNA profiling. We help researchers analyze the gene expression patterns, detect novel transcripts, examine alterations in the transcriptome, study DNA-RNA interactions, DNA-protein interactions, and more. enabling a deeper understanding of nucleic acid biology and disease development. In addition to NGS, we provide comprehensive research technologies such as ChIP sequencing, ATAC sequencing, and chromosome conformation capture sequencing (3C-Seq).

Features

Service Portfolio

Explore how our innovate technologies help you understand nucleic acid dynamics through sequencing and bioinformatic analysis.

ChIP Sequencing

ChIP-Seq detects the interaction between proteins and DNA through the specificity of the antigenic antibody response.

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ATAC Sequencing

ATAC-Seq detects the open regions of chromatin on a genome-wide scale.

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Chromosome Conformation Capture Sequencing (3C-Seq)

3C-Seq interprets the interaction patterns among different DNA sequences, as well as providing high-resolution chromatin three-dimensional structure information.

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Application Fields

  • Cancer transcriptomics
  • Population genetics
  • Pharmacogenomics applications
  • Agricultural applications

Sequencing Platforms

  • Illumian HiSeq 2500 / HiSeq 4000 / HiSeq X Ten / NovaSeq 6000 / NextSeq 500 / MiSeq
  • PacBio RS II / Sequel
  • Nanopore PromethION
  • 10X Genomics
* For Research Use Only. Not for use in diagnostic procedures.


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