CD Genomics

The Genomics Services Company

Featured
Sequencing Solutions
in CD Genomics
 CD Genomics
The Genomics Services Company

Sequencing technologies, genomics, and bioinformatics are rapid and effective

tools to study phage genomics. In addition, further analysis, including transcription,
translation, regulation, and modification, are also emerging techniques that are
extremely helpful in exploring the life cycle, specificity, lytic ability, and lysogenicity
of phages. Today, a large amount of genomic data has been integrated after being
CD Genomics generated at high speed, which provides a strong foundation for the use of phages
in personalized medicines and scientific research.
An Expert in Sequencing &
Bioinformatics

FAST · COMPLETE · RELIABLE

About Us
CD Genomics is a globally recognized company for providing innovative and customized genome
sequencing services and products to the life science industries and academic research institutions.

At CD Genomics, we are constantly seeking for faster and more efficient ways to solve customer
challenges.

Our expert team is capable of achieving more precise and accurate sequencing results for
customers. We can execute projects from start to finish by delivering services such as project design,
sample processing, sequencing, and data analysis. In addition to standardized genomic
services, we can also provide customized sequencing services and design bioinformatics pipelines
according to your specific research needs, maximizing effectiveness and cost efficiency for research
and development.

CD Genomics Platforms Flexible & Reliable

At CD Genomics, our services adapt to a variety Illumina MiSeq / NextSeq 500 / NovaSeq
of advanced sequencing technologies and
platforms from world-leading vendors, and 6000
researchers will be able to identify tools that best
suit their research needs with flexibility. We are PacBio Sequel II
also capable of offering complete support for
researchers from preclinical research to clinical Nanopore MinION / Promethlon
applications, accommodating standardized and
scale-up requirements for genomic analysis, as MGI DNBSEQ-T7 / DNBSEQ-G400
well as performing large-scale translations.
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Whole Genome Sequencing

The most detailed view of genetic code

Whole genome sequencing provides a detailed insight into genetic variations encoding human
and mouse traits and diseases, covering from single nucleotide changes to chromosomal
rearrangements. Our team of sophisticated scientists is able to resolve all sample types to
accelerate the progress of small to large projects, such as disease genomics and population
genetics.

Species: Human / Mouse

Platforms: Illumina, PacBio, and Nanopore

Sample Type: Cells, blood, tissue, FFPE, and other samples

Sample Requirements: Genomic DNA, Illumina ≥ 200 ng; PacBio/Nanopore ≥ 3 μg;

A260/280=1.8-2.0; A260/230=1.5-2.6; no degradation and contamination

Whole Exome Sequencing

Discover or interrogate SNPs, indels or structural variants
Whole exome sequencing adapts to advanced target-capturing technology capable of quickly
extracting sequence information for the entire exome and helps you screen for useful
genomic variants, germline/somatic mutations, and potential pathogenic mechanisms by
enhancing sequencing depths and reducing sequencing costs.

Species: Human / Mouse

Platform: Illumina

Sample Type: Cells, blood, tissue, FFPE, and other samples

Sample Requirements: ≥ 300 ng; A260/280=1.8-2.0; no degradation and contamination

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Microbial Genomics
Interrogate genetic mutations or investigate microbial communities
within samples
The microbial genome sequencing platform has been developed for samples of different
sources to serve various application purposes, including but not limited to public health,
infectious disease research, molecular epidemiology, and industrial microbial development
research. With years of experience in sequencing and assembling genomes of known and
novel microorganisms, we are capable of detecting and interpreting genetic mutations, evolu-
tion, and more.

16s
Rapid metagenomic analysis of bacterial Platform: Illumina, PacBio, and Nanopore
populations using the amplicon sequencing
technology. Sample Requirements: Illumina ≥ 100 ng;
The 16s strategy targets the 16s rRNA PacBio/Nanopore ≥ 100 ng;
region of bacteria to determine microbial
A260/280=1.8-2.0; no degradation and
diversities, microbial abundances, and
possible microbial functions. contamination

Microbial Whole Genome Sequencing

Whole genome sequencing and Platform: Illumina, PacBio, and Nanopore
assembly of bacteria, fungi, viruses, or
other microorganisms. Sample Requirements:
Microbial whole genome sequencing is Illumina: prokaryotic/eukaryotic DNA/cDNA
generally used for the elucidation of
known species and the discovery of new amount ≥ 0.5 μg, viral DNA/cDNA amount ≥
biomarkers or low-frequency 1 μg; PacBio: bacterial DNA amount ≥ 3 μg,
mutations. Also, we are capable of
sequencing accurate genomes of novel fungal DNA amount ≥ 3 μg;
species for projects such as microbial A260/280=1.8-2.0; no degradation and
identification, comparative genomic contamination
research, and the development of
industrial microbial strains.

Metagenomics
Achieve all genetic and genomic Platform: Illumina, PacBio, and Nanopore
information of mixed communities in a
single sample. Sample Requirements:
Metagenomics helps to understand the Illumina ≥ 100 ng;
interactions between microbiome and
host or environmental factors, including PacBio/Nanopore ≥ 3 μg;
non-culturable and unknown microor- A260/280=1.8-2.0;
ganisms, for the study of human micro-
biome and diseases, or interactions of no degradation and contamination
plant and microbe, etc.
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RNA Sequencing
Provides valuable information on cellular mechanisms, genome
structure, disease-inducing effects and more
RNA sequencing is capable of qualitatively and quantitatively detecting a wide range of RNAs in
biological samples at specific time points. Our RNA sequencing service covers basic studies of
cell structure and function to detect and analyze various disease states. We have experience
detecting alternative splicing, post-transcriptional modifications, and analyzing exon-
intron boundaries.

Platforms: Illumina, PacBio, and Nanopore

Sample Type: Cells, blood, tissue, FFPE, and other samples

Solution Options:

Single-Cell RNA-Seq LncRNA Sequencing

Ultra-Low Input RNA-Seq Degradome Sequencing

Iso-Seq Targeted RNA Sequencing

Strand-Specific RNA-Seq Exosomal RNA Sequencing

Small RNA-Seq Dual RNA-seq

More Services...

Epigenomics Sequencing
Facilitates the research of DNA/RNA modifications and DNA/RNA,
protein interactions
Epigenomic sequencing employs various sequencing technologies (comprehensive NGS and
long-read sequencing) and platforms to study genomic alterations, i.e., DNA/RNA methylation,
DNA/RNA protein interactions, chromatin accessibility analysis, histone modifications, etc.

Platforms: Illumina, PacBio, and Nanopore

Sample Type: Cells, blood, tissue, FFPE, and other samples

Solution Options:

Methylation Sequencing RRBS

Long-read Methylation Seq hMeDIP-Seq

ATAC-Seq MeRIP-Seq

ChIP-Seq RIP-Seq

MeDIP-Seq oxBS-Seq

BS-Seq Methylation Microarray

More Services...
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Flexible Workflows
End-to-end solutions to drive scientific discovery more rapidly and
efficiently

Sample Preparation
• Handle any sample that yields DNA or RNA (e.g., cell cultures, fresh-fro-
zen tissues, formalin-fixed paraffin-embedded (FFPE) tissues, blood,
saliva, etc.)
• Optimized extraction protocols based on your requirement for highest
quality and quantity

Generate Sequencing library

• Prepare templates in hours with easy-to-use workflow for NGS or

long-read sequencing
• Multiplex and unique identifier to increase throughput

Sequencing

With our diverse sequencing systems, you can:

• Access reference-quality assemblies of animal, plant and microbiome
samples
• Phase diploid genome assemblies
• Identify single nucleotide polymorphism, indels, copy number variants
and structural variants

Bioinformatics & Data Analysis

Explore intuitive findings for your Oncology, Pathology, and Immune

research
• NGS Data Analysis
• SMRT Data Analysis
• Nanopore Data Analysis

Contact CD Genomics for more inspiration and service content.

CD Genomics
The Genomics Services Company