Pricing Tables

NovaSeq runs include additional cycles for dual indexed libraries.

1.5B10B25B
100 cycle: $3,200100 cycle: $8,400100 cycle: $13,100
200 cycle: $3,700200 cycle: $10,300
300 cycle: $4,000300 cycle: $10,900300 cycle: $17,800

 

NovaSeq X Plus Lane Pricing

10B: ~2.5 billion reads per lane
300 cycle: $1400

NovaSeq X Plus Lane Order

10B: ~2.5 billion paired reads, $1400

NovaSeq X Plus Flow Cell Order

1.5B: ~3 billion paired reads, 10B: ~20 billion paired reads, 25B: ~50 billion paired reads

Novaseq X Plus

We now offer runs on the new Novaseq X Plus platform. If you require NovaSeq 6000 please contact David Mohr for details

NovaSeq X

novaseq-x-sequencer-with-background-of-flow-cell-compartment-close-up

GRCF High Throughput Sequencing Center

 

Our goal is to provide the Johns Hopkins community access to Next Generation sequencing platforms.

 

We currently feature  MiSeq and NovaSeq X Plus instruments. We do our best to sequence samples in a timely manner, but our primary focus is on generating high quality data.

Sample Requirements

NovaSeq Runs

For NovaSeq runs, please submit at least 50ul of your sample at 4nM.

Pooling

Samples should be pooled.

QC Preferences

Nanodrop is not reliable. Intercalating dye methods or qPCR are preferred.

MiSeq Runs

Please submit 10μl of your sample at 2nM for MiSeq.

Quality Control

We will do a QC check via Bioanalyzer to increase the likelihood of quality data, but you should quantitate your sample as accurately as possible prior to submission.

Questions

Please contact us with any sample preparation questions.

DNA or total RNA

Please provide us with ~500ng of high molecular weight DNA or total RNA >6.5.

Low yield

There are a host of options for lower input/lower quality that may add cost.

Cost

$250/sample

Questions

Please contact us to discuss sample submission or any questions you may have regarding library preparation.

Understanding Data Yield

Our facility features the NovaSeq platform. Yield is dependent upon several factors:

Read Length & Read Type

The longer the read, the more data. Paired end reads yield twice the data as single read.

Read Length & Read Type

The longer the read, the more data. Paired end reads yield twice the data as single read.

Optimal Cluster Density

It is imperative to accurately quantitate your library to ensure high data yield. We do our best to QC libraries before sequencing, but we cannot pool samples for you.

High Quality Library

Libraries that contain a high level of adapter dimers will yield significantly less data, particularly on the NovaSeq6000. Similarly, over amplified libraries can negatively impact yield

Please see Illumina’s  NovaSeq X Specification page for current data yields. While we regularly achieve greater than ‘spec’ yields from the NovaSeq X, it is best to be conservative when planning your experiments.

Data Delivery

Per lane/flowcell sequencing

Data will be returned in Sanger FASTQ format via our high speed aspera server.

End to end services

Alignment files, variant calls, and any intermediate files you wish via aspera server.