Download

RNA-Binding Proteins (RBPs) Study Strategies

CUT&Tag Seq: Efficient Chromatin Profiling for Histone & TF Analysis

Power Your Regulatory Discoveries with DAP-seq: A MYB–GLK Case Study

EM-seq Services for High-Resolution DNA Methylation Analysis

Multi-Omics Strategies to Decode Molecular Mechanisms at Every Level

Explore Customized Bioinformatics Services: Case Studies & Insights

RNA-seq, ATAC-seq, and CRISPR Screening: Powering CAR T-Cell Research

Integrated Analysis of ChIP-seq and RNA-seq: Decoding Pancreatic Cancer Stem Cell Mechanisms

AAV Integration Site Analysis: Safeguard Against Insertional Mutagenesis Risks

Off-Target Validation Available Now: Maximize Your CRISPR Success

RNA Methylation Analysis: Choosing the Right Method

Enhancing Biological Research with CD Genomics' Bioinformatics Support

Choose the DNA Methylation Microarray Service that Fits Your Needs- 270K or 935K?

10x Spatial Transcriptome Sequencing Service Solutions

2b-RAD Sequencing: Your Gateway to High-Density SNP Genotyping

Microbiome Sequencing Solutions

Plasmid/Phage Sequencing: Unlocking the Power of Engineering Tools

Population Genetics and Sequencing Solutions

PacBio SMRT Sequencing Solutions

Genotyping Solutions

Nanopore Sequencing Service

How to Design Your CircRNA Research With Sequencing

Why Now Is the Perfect Time for LncRNA Research

Revolutionize Research: NGS Microbiome Analysis for Deeper Insights

Cutting-Edge High-Throughput Sequencing Services: A Comprehensive Guide

A Beginner's Guide to Study RNA-Protein Interactions with RIP-Seq

How to Accelerate Your Infectious Pathogens Research by Sequencing

Sample Submission Guidelines

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?