Method for shotgun DNA libraries used for whole genome sequencing.
(*) For unextracted samples.
(**) Turnover times are not guaranteed, may change according to your project.
Accepted Sample Type | Recommended Amount | Shipment method |
---|---|---|
Whole Blood (Fresh or Frozen) | 650μL-1ml | Blue ice for fresh blood Dry ice for frozen blood |
Buccal Swab | Follow the kit manufacturer's instructions | |
Tissue | 30 - 50 mg | Dry ice |
FFPE Tissue |
|
Room temprature |
Cell Pellet |
|
Dry ice |
Saliva | 650μL-1mL | Dry ice or blue ice |
Genomic DNA (RNA-free) | 50μL, >20 ng/μL | Dry ice |
We check your samples upon arrival however, we still require our users to do their own QC steps before sending samples.
Please use fluorometric measurements (e.g. Qubit, Quant-it), not absorbance measurements (Nanodrop, spectrophotometer).
The DNA should be in EB buffer (not EDTA or water), of high quality, and ideally have an A260/280: 1.8- 2.0 and A260/230: 2.0 – 2.2
If your samples are below the required thresholds, please get in touch.
Once your samples arrive at SZAOMICS, we start by performing a reception control step in which we make sure the samples meet our requirements.
If the samples fail this quality control step, we will contact you to discuss possible options. Should you choose to proceed with samples not fulfilling the criteria it will be at your own risk, SZAOMICS will only make one attempt at library preparation and if the prep does not work you will have to pay for the library preparation anyway.
If the samples pass reception control, we will inform you and the samples will be queued for library preparation.
Illumina’s new tagmentation-based DNA PCR-free library preparation is the method of choice for generating the highest quality DNA sequencing libraries. PCR-free libraries have better coverage of GC-rich regions compared to PCR-based methods and the reads are more evenly distributed over the genome.
This method is recommended when:
Library QC and sequencing: We evaluate the concentration of the library and inform you of the QC status of each sample. Once the libraries have passed this QC step, they are normalized, pooled, and queued for sequencing.
PCR-free libraries are well suited for deep sequencing to achieve high coverage genomes. The library preparation method shows a significantly better coverage of GC-rich regions compared to PCR-based methods and the reads are more evenly distributed over the genome.