Animal and Plant De novo Sequencing

De novo sequencing generates an initial genomic sequence of a particular organism without a reference sequence. Through de novo sequencing, complex genomic variations such as Indel, CNV, and SV can be easily identified. It is also valuable in evolutionary and demographic history, agricultural breeding, and genetic variations calling.

Category:

With extensive experience in experimental operations and bioinformatics analyses, Novogene offers an accurate, rapid, and comprehensive characterization of species and generates reliable results. Furthermore, Novogene’s end-to-end services guarantee you ultra-fast turnaround time.

Applications

For individual research:

  • Guides animal health and genetic breeding
  • Provides a theoretical basis for drug screening
  • Explores medicinal resources and innovates varieties

For population research:

  • Explores species origin and evolution
  • Provides new insights into patterns of genome divergence

Applications

For individual research:

  • Guides animal health and genetic breeding
  • Provides a theoretical basis for drug screening
  • Explores medicinal resources and innovates varieties

For population research:

  • Explores species origin and evolution
  • Provides new insights into patterns of genome divergence

Benefits

Highly experienced: Novogene’s highly qualified researchers have completed major De novo genome sequencing projects and managed to publish their data in top-tier journals.

Bioinformatics expertise: Best-in-class and widely recognized software, such as Falcon and Canu, are being used for comprehensive plant and animal bioinformatic analyses.

Diverse strategies: By incorporating sequencing results from various platforms including Illumina Novaseq, PacBio Revio/Sequel II/Sequel IIe, and Oxford PromethION, we offer the best assembly solution specifically tailored for each unique genome.

Unsurpassed data quality: We guarantee a Q30 score ≥ 85%, exceeding Illumina’s official guarantee of ≥ 75%.

Specifications: DNA Sample Requirements

Platform Type Sample Type Amount (Qubit®) Purity
Illumina
NovaSeq 6000
Genomic DNA ≥ 200 ng A260/280=1.8-2.0;
no degradation,
no contamination
Genomic DNA
(PCR free non-350bp)
≥ 5 μg
Genomic DNA
(PCR free -350bp)
≥ 1.2 μg
PacBio Sequel II
DNA CLR library
HMW Genomic DNA ≥ 5 μg
(Concentration ≥ 70 ng/μL)
A260/280=1.75-2.0;
A260/230=1.5-2.6;
NC/QC=0.95-3.00
Fragments should be ≥ 30 kb
PacBio Revio/sequel II/sequel IIe DNA HiFi library HMW Genomic DNA ≥ 15 μg
(Concentration ≥ 70 ng/μL)
A260/280=1.8-2.0;
A260/230=1.5-2.6;
NC/QC=1.00-2.20
Fragments should be ≥ 30 kb
Nanopore PromethION HMW Genomic DNA ≥ 8 μg
(Concentration ≥ 100 ng/μL)
A260/280=1.75-2.0;
A260/230=1.4-2.6;
NC/QC=0.95-3.00
Fragments should be ≥ 30 kb

NC/QC:NanoDrop concetration/Qubit concentration

Specifications: Sequencing and Analysis

Sequencing Parameters Illumina Novaseq 6000 PacBio Revio/sequel II/sequel IIe Nanopore PromethION
Read Length Paired-end 150 bp N50>15 kb, long read lengths up to 25 kb(CCS) average > 17 kb
Recommended  Sequencing Depth For genome survey or assembly polishing: ≥ 50× For genome assembly: ≥ 50×
Standard Analysis K-mer analysis

GC content analysis

Repeat content rate evaluation

Heterozygous rate evaluation

Genome size evaluation

Long-read assembly

Assembly Statistics

Gene completeness evaluation

Genome Annotation Repeat prediction

Structure prediction

Function prediction

Noncoding RNA prediction

Project Workflow

Animal and Plant Whole Genome Sequencing

From sample preparation library preparation, short and long-read sequencing, and data quality control, to bioinformatics analysis, Novogene provides high-quality products and professional services. Each step is performed in agreement with a high scientific standard and meticulous design to ensure high-quality research results.

GeneSmart tự hào là đơn vị tiên phòng đầu tiên tại Việt Nam cung cấp giải pháp:

1. Giải trình tự tế bào đơn (SINGLE-CELL SEQUENCING);

2. Chuẩn bị mẫu tự động (AUTOMATED LIQUID HANDLING);

3. Xét nghiệm và chẩn đoán bệnh nhiễm (DIAGNOSIS OF INFECTIOUS DISEASE);

4. Sinh chiết lỏng (LIQUID BIOPSY)

5. Giải phẫu bệnh sinh học phân tử (MOLECULAR PATHOLOGY)

6. Nghiên cứu ung thư (CANCER RESEARCH)

7. Nghiên cứu miễn dịch (IMMUNOLOGY)

8. Khoa học hình sự (FORENSIC)

9. Trữ mẫu sinh học (Ngân hàng sinh học, BIOBANKING)

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