- HOME
- Products & Services
- Application Selection Guide
- Custom Data Analysis
-
Oligonucleotide API CDMO
-
Custom DNA/RNA Systhesis
-
Next Generation Sequencing
- Next Generation Sequencing
-
Application Selection Guide
- Application Selection Guide
- Human Genome Sequencing
- Whole Genome Sequencing (Non-Human)
- Microbial genome sequencing
- Small scale sequencing (NGS Petit)
- GRAS-Di® Genotyping
- Repeat Motif Detection
- Library Prep for Challenging DNA Samples
- Gene Expression Analysis (Reference-Based)
- Isoform Sequencing (full-length mRNA-seq)
- De novo Transcriptome Sequencing
- Small RNA-Seq
- Microbial Community Analysis
- Shotgun Metagenomic Sequencing
- Metatranscriptome Sequencing
- ChIP-Seq
- CRISPR Screening
- Illumina Amplicon Sequencing
- PacBio Amplicon Sequencing
- Standard Pipeline Data Analysis
- Custom Data Analysis
- Gene Analysis from Pathological Specimens
- Sequencer Models and Sequencing Principles
- Sample Requirements
- How to Order
- Scientific Publications
-
Custom DNA Sequencing
-
Custom DNA Microarray
-
Protein Related Service
-
Laboratory Tools and Service
- Nucleic Acid Extraction
- RNA Purification
- RNA Quality Control
- Custom Measurement for synthetic DNA Molecular Weight
- Full-length cDNA library Production Service
- Stock Series
- LaboPass™ Products Series
- Koro Koro Rack
- Ukkie
- 8-tube strip
- Rhodococcus erythropolis Protein Expression System
- LipoTrust™ Series
Custom Data Analysis
Overview
We offer comprehensive data analysis services for raw data obtained either in our facility or from external sources.
If you have sequencing data from your own NGS equipment, a nearby sequencing facility, or another service provider, we can process it for you. Feel free to contact us if you need assistance with data analysis.
Workflow
Example Inquiries
– Extract reads specific to the target organism from contaminated sample data and perform assembly.
– Search for specific gene or protein sequences from transcript sequences obtained via RNA-Seq.
– Compare two closely related bacterial genomes to identify unique regions in one strain and design primers accordingly.
– Use fragmented amino acid sequences obtained from N-terminal protein analysis to extract corresponding transcript sequences from RNA-Seq data.
– Edit and convert data into a format compatible with existing analysis software or pipelines.
– Reanalyze previously processed data using the latest database information.
– Perform reanalysis using data obtained over multiple experiments by rearranging sample combinations.
– Utilize analysis programs referenced in scientific papers to analyze user-provided data.
– Generate publication-ready figures based on NGS data, following reference literature.
– Assist with data submission to DRA, DDBJ, or GEO databases.
The above are just a few examples. If you have any specific requirements, please do not hesitate to contact us.
Back to "Products & Services"