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Eukaryotic mRNA Sequencing-NGS

mRNA sequencing is a technique that uses next-generation sequencing to reveal the presence and quantity of RNA molecules in a biological sample, providing a snapshot of gene expression in the sample.

With its wide-ranging applications, this cutting-edge tool unveils intricate gene expression profiles, gene structures, and molecular mechanisms associated with diverse biological processes.

This technique is widely adopted in research, clinical diagnostics, and drug development, since it offers insights into the intricacies of cellular dynamics and genetic regulation, providing a sturdy base to spark curiosity about its potential on different fields.

 

Platforms available: Illumina NovaSeq X; DNBSEQ-T7


Service Details

Bioinformatics

Demo Results

Featured Publications

Features

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● Optional directional mRNA library preparation to enable obtaining strand-specific sequencing data

● Different BI analysis cover all our clients needs

 

Advantages

● Extensive Expertise: We have processed over 600,000 samples, spanning diverse sample types such as cell cultures, tissues, and body fluids. We bring the wealth of expertise to every project.

● Rigorous Quality Control: We implement core control points across all stages, from sample preparation to library preparation, sequencing and bioinformatics. Our meticulous monitoring ensures the delivery of consistently high-quality results.

● Comprehensive Annotation: We use multiple databases to functionally annotate the Differentially Expressed Genes (DEGs) and perform corresponding enrichment analyses. This comprehensive approach provides insights into the cellular and molecular processes underlying the transcriptome response, ensuring you get all the information possible about your experiment’s data.

● Post-Sales Support: We understand how important is to be present, that’s why our commitment extends beyond project completion with a 3-month after-sale service period. During this time, we offer project follow-up, troubleshooting assistance, and Q&A sessions to address any queries related to the results.

Sample Requirements and Delivery

Library Sequencing strategy Data recommended Quality Control
Poly A enriched

Illumina PE150

DNBSEQ-T7

6 -10 Gb

Q30≥85%

Sample Requirements:

Nucleotides:

Mimimum Sample Requirements:

 

Conc.(ng/μl)

Amount (μg)

Purity

Integrity

Standard Library

≥ 10

≥ 0.2

OD260/280=1.7-2.5

OD260/230=0.5-2.5

Limited or no protein or DNA contamination shown on gel.

For plants: RIN≥4.0;

For animals: RIN≥4.5;

 5.0≥28S/18S≥1.0;

limited or no baseline elevation

Directional Library

≥ 10

≥ 0.2

OD260/280=1.7-2.5

OD260/230=0.5-2.5

Limited or no protein or DNA contamination shown on gel.

For plants: RIN≥4.0;

For animals: RIN≥4.5;

 5.0≥28S/18S≥1.0;

limited or no baseline elevation

Plants Animal Arthropods Whole blood Cells

Root, Stem or Petal: 450 mg

Leaf or Seed: 300 mg

Fruit: 1.2 g

HEart or Intestine: 300 mg

Viscera or Brain: 240 mg

Muscle: 450 mg

Bones, Hair or Skin: 1g

Insects: 6g

Crustacea: 300 mg

1 tube 106 cells

Recommended Sample Delivery

Container: 2 ml centrifuge tube (Tin foil is not recommended)

Sample labeling: Group+replicate e.g. A1, A2, A3; B1, B2, B3... ...

Shipment:

1. Dry-ice: Samples need to be packed in bags and buried in dry-ice.

2. RNAs table tubes: RNA samples can be dried in RNA stabilization tube(e.g. RNAstable®) and shipped in room temperature.

Sample Requirements and Delivery

Sample QC

Experiment design

sample delivery

Sample delivery

Pilot experiment

RNA extraction

Library Preparation

Library construction

Sequencing

Sequencing

Data analysis

Data analysis

After sale Services

After-sale services


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  • Bioinformatics

    For samples with an available reference genome, the BI analysis is as it follows:

    Bioinformatic Analysis Pipeline-01(1)

    Ø  Raw data quality control

    Ø  Reference genome alignment

    Ø  Transcript structure analysis

    Ø  Expression quantification

    Ø  Differential expression analysis

    Ø  Function annotation and enrichment

     

    For samples without a reference genome, this is the option available:

    Bioinformatic Analysis Pipeline-02(1) Raw data quality control

    • Assembly with structure optimization

    • Differential expression analysis

    • Function annotation and enrichment

     

     

      Reference Genome Alignment

     

    图片1

     

    Data Saturation 

     

    3(1)

     

     

    Sample correlation and assessment of biological replicates

     

    图片2

     

    Differentially Expressed Genes (DEGs)

     

    4(1)

     

     

    Functional Annotation of DEGs

     

    6(1)

     

     

     

    Functional Enrichment of DEGs

     

    图片4

     

    Explore the advancements facilitated by BMKGene’s eukaryotic NGS mRNA sequencing services through a curated collection of publications.

     

    Huang, L. et al. (2023) ‘Triclosan and triclocarban weaken the olfactory capacity of goldfish by constraining odorant recognition, disrupting olfactory signal transduction, and disturbing olfactory information processing’, Water Research, 233, p. 119736. doi: 10.1016/J.WATRES.2023.119736.

    Jia, L. J. et al. (2023) ‘Aspergillus fumigatus hijacks human p11 to redirect fungal-containing phagosomes to non-degradative pathway’, Cell Host & Microbe, 31(3), pp. 373-388.e10. doi: 10.1016/J.CHOM.2023.02.002.

    Jin, K. et al. (2022) ‘TCP Transcription Factors Involved in Shoot Development of Ma Bamboo (Dendrocalamus latiflorus Munro)’, Frontiers in Plant Science, 13, p. 884443. doi: 10.3389/FPLS.2022.884443/BIBTEX.

    Wen, X. et al. (2022) ‘The Chrysanthemum lavandulifolium genome and the molecular mechanism underlying diverse capitulum types’, Horticulture Research, 9. doi: 10.1093/HR/UHAB022.

    Zhang, Yujie et al. (2023) ‘A cascade nanoreactor for enhancing sonodynamic therapy on colorectal cancer via synergistic ROS augment and autophagy blockage’, Nano Today, 49, p. 101798. doi: 10.1016/J.NANTOD.2023.101798.

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