Explore the scientific documents we’ve developed, including sample submission guidelines, principles, applications, and bioinformatics of genetic technologies.
Full-Length Transcriptome Sequencing
HLA Typing
Featured Sequencing Services in CD Genomics
Ribosome Profiling, A Powerful Sequencing Tool for Translatome Research
Whole Exome Sequencing (WES)
TCR/BCR Sequencing & HLA Typing
CD Genomics NGS Panel One-Stop Solution
Lentiviral Integration Sites Analysis
NGS CRISPR Sequencing Solutions
Sequencing Approach Enables More In-depth Phageome Investigation
Minimize the Off-Target Effects of CRISPR Genome Editing with Next-Generation Sequencing
Immune Repertoire Sequencing
Sequencing or Array-Based Genotyping
Introduction of CD Genomics
Plan Your Next Exosome RNA Sequencing Experiment
Sequencing Technologies for DNA 5mC/5hmC Modifications
CD Genomics, An Expert in Sequencing & Bioinformatics
How to explore cancer-related mutations using NGS
Gene Mutation and Expression Profiling with Transcriptome Sequencing
Powerful Solutions for Exploring Epigenomic Changes
Genomics Transforms the Future of Agriculture
Insight into Tumor Heterogeneity through Next-Generation Sequencing
Genomics Technologies Transform the Future of Biomarker Discovery
How to Choose the Best 16S/18S/ITS Sequencing Method for Your Project?
Sequencing-Based Methods for Profiling DNA Methylation
Genome-Wide Profiling of Histone Modifications with ChIP-Seq
Chromatin Accessibility Assays: ATAC-Seq, DNase-Seq, MNase-Seq and FAIRE-Seq
NGS Panel: Hybridization Capture or Amplicon Sequencing?
Long-Read Sequencing: PacBio SMRT vs. Oxford Nanopore
RNA-Seq Library Preparation: Comparing the rRNA Depletion Methods
How to Perform Bioinformatic Analysis for Microbial Sequencing Data
How Can Single-Cell Sequencing Facilitate Tumor Research?
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