$15 / Whole Plasmid Sequencing

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Same Day Results

Results delivered the same day samples are received

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$15 per plasmid.

Sequencing verification for a fraction of the price

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Full-Length Plasmids

Get the complete picture of your plasmid from 5kb - 30kb

Same Great Sequencing / Without the Primers

Fast, accurate, and affordable long-read sequencing

Confirm your full plasmids faster, more accurately, and more affordably than ever before. NGS generation 3 technology has made it possible to quickly sequence whole plasmids in a fraction of the time and without the hassle of having to design and synthesize primers. The typical turnaround time for whole plasmid sequencing is 1 business day measured from when the samples are received. There is no minimum requirement for the number of samples.

 

How to order

Order in tubes

Order in plates

 

Sample Submission Guidelines

The following table contains all samples types, not only whole plasmid sequencing.  

Sample type Category Size Concentration Min volume Price per sample Nanocoins Turnaround time
(biz days)**
Component #
Plasmid Regular 2.5 - 25 kb 30 ng/uL ≥10 uL $15 1 1 3010-WPSPM
Large 25 - 125 kb 50 ng/uL ≥20 uL $30 2 1 3010-WPSPL
XL 125 - 300 kb 50 ng/uL ≥40 uL $60 4 1 3010-WPSPXL
Linear/Amplicon Regular 600 bp - 25 kb 30 ng/uL ≥10 uL $15 1 1 3010-WPSAM
Large 25 - 125 kb 50 ng/uL ≥20 uL $30 2 1 3010-WPSAL
Bacterial Genome Regular up to 7 Mb 50 ng/uL ≥50 uL $90 6 2 3010-WPSBM
Large 7 - 12 Mb 50 ng/uL ≥50 uL $105 7 2 3010-WPSBL
Yeast  Regular <20 Mb 50 ng/µL 20 µL $150 10 2 3010-ONTYEST
AAV Regular 2.5 - 25 kb 30 ng/uL ≥10 uL $15 1 1 3010-ONTAAVM
Large 25 - 125 kb 50 ng/uL ≥20 uL $30 2 1 3010-ONTAAVL
XL 125 - 300 kb 50 ng/uL ≥40 uL $60 4 1 3010-ONTAAVXL
Premium PCR Sequencing Regular 3000 reads * ≥10 uL $30 2 1 3010-ONTLSM
Large 6000 reads * ≥20 uL $60 4 1 3010-ONTLSL
XL 12,000 reads * ≥40 uL $120 8 1 3010-ONTLSXL
XXL 100,000 reads * ≥40 uL $490 67 1 3010-ONTLSXXXL
Custom Sequencing Base service 100 bp to a massive 300 kb * See product info $500 up to 1 Gb n/a 2 - 4 3010-ONTCUS
Addl. Data * See product info $50 per addl Gb n/a n/a 3010-ONTCUSA
Barcoding * See product info $50 per sample if multiplexing n/a n/a 3010-ONTCUSB

*See product webpage for details.

**Turnaround time is measured from the day the samples leave the customer's hands. Results are actually delivered the same day the samples arrive in our lab. For example, if samples were shipped on Monday, the samples would arrive overnight on Tuesday and results would be delivered Tuesday morning.

 

 

 

 

Common Questions

How do I ship samples?

1. Dropbox - we have a nationwide network of dropboxes. If you want a box for your lab, let us know! Email GenomicsSupport@eurofins.com to request a box.

2. Free Digital Shipping Labels - digital shipping labels are provided free for a vast majority of sequencing orders. You can select the option for digital shipping label during checkout. Take a look at our sample submission options page for more details.

3. Ship the samples using your normal carrier - If using your own carrier, we highly recommend shipping overnight/next-day delivery to ensure the samples do not degrade in transit.

How do I get results?

Results are available to download from the order history page. You will be emailed when the results are ready as well. Currently, 95% of results are delivered within 1 business day from receiving the sample.

What data files will I receive? 

Visit the Data Deliverables webpage for more information.

The Easiest Possible Way to / Sequence

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No Primers Needed

Unlike short-read sequencing, whole plasmid sequencing does not require any primers.

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No library prep needed

Unlike conventional next generation sequencing methods, no library prep is required.

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No Shipping Cost

You can use our existing network of dropboxes to submit samples or print a free digital shipping label after checkout for qualifying orders.

98

Accuracy

Oxford Nanopore’s reports the raw read accuracy is 98.3% and the consensus accuracy for SNPs is 99.6% with 50X coverage.

Benefits / and Advantages

Benefits

- Long read recovery of several kilobases
- Great for GC rich or repetitive DNA
- Detect E. coli and genomic DNA carryover
- Faster TAT compared to traditional primer walking and plasmid verification techniques
- Lower cost than traditional NGS methods
- Verification of the entire vector sequence
- Scalable
- Available from one sample
- 5 - 4 million reads per Flow Cell (dependent on DNA quality and length)

Applications

Whole plasmid sequencing using NGS Gen 3 technology is a powerful and accurate method for characterizing and analyzing plasmids, which makes it well suited for a wide range of applications.

- Plasmid Verification
- Resequencing of whole genomes
- Assembly of genomes
- Identification of taxonomic background
- Metagenomic analysis of long reads
- Much more.

Easy to Submit

- No primers required! It could not be easier
- Requires less DNA than short-read sequencing
- Super simple order page
- Turnaround is typically 1 business day, measured from when samples arrive
- Nationwide network of dropboxes
- No dropbox near you? No problem. Eurofins Genomics is the only company that offers free digital shipping labels.

Sample Submission Guide / and FAQ


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