Multiomics
Pre-made Library Sequencing
Pre-made Library Sequencing
Mirxes Genomics provides standalone sequencing service to researchers preparing their own libraries. We work with strict quality controls and optimized sequencing workflows to deliver high-quality data for your research. We accept various types of pre-made libraries for sequencing on high-throughput DNBSEQ-T7 and T10 platforms.
Experience in sequencing a wide variety of libraries:
Illumina
- TruSeq DNA
- TruSeq RNA
New England Biolabs
- NEBNext
10x Genomics
- Chromium Single Cell Gene Expression Flex
- Chromium Next GEM Single Cell 3ʹ
- Chromium Next GEM Single Cell 5’
- Chromium Single Cell 3′ with Feature Barcoding
- Chromium Next GEM Single Cell ATAC
- Visium Spatial Gene Expression
Olink
- Olink Explore
Mission Bio
- Tapestri
MGI Tech
- MGI DNBelab C4
Dovetail
- Micro-C
We are able to convert most Illumina-compatible libraries for DNBSEQ sequencing.
Do contact us if you would like to explore libraries beyond what is listed above.
High Quality Data
Q30 score of >85% for PE150 and PE100
Cost Efficiency
Revolutionizing the cost of sequencing with ultra-high throughput
Sequencing
Bioinformatics
| Service | Optimum Input Amount | Volume | Library Concentration | Library Size |
|---|---|---|---|---|
| Pre-made library sequencing | ≥ 200ng | ≥ 20μl | ≥ 2ng/μl | 200 – 700 bp |
Please note that these requirements serve only as a guide. Please contact us for further assessment if your samples do not meet the requested amounts
- Sequence alignment file (BAM)
- Gene count matrix
- QC statistics (cell barcode, UMI, and alignment statistics)
- Data curation
- Clustering
- Annotation
- DEG
- Pathway analysis
- CNV (for tumor)
- Pseudo-temporal analysis
- Many other options!