SP: ~1.6 billion paired reads, S1: ~3.2 billion paired reads, S2: ~8.2 billion paired reads, S4: ~20 billion paired reads
GRCF High Throughput Sequencing Center
Our goal is to provide the Johns Hopkins community access to Next Generation sequencing platforms.
NovaSeq runs include additional cycles for dual indexed libraries.
|SP: ~1.6 billion paired reads, ~800 million single reads||S1: ~3.2 billion paired reads, ~1.6 billion single reads||S2: ~8.2 billion paired reads, ~4.1 billion single reads||S4: ~20 billion paired reads, ~10 billion single reads|
|100 cycle: $3960||100 cycle: $6600||100 cycle: $10230|
|200 cycle: $4730||200 cycle: $7700||200 cycle: $12210||200 cycle: $17600|
|300 cycle: $5060||300 cycle: $8250||300 cycle: $12760||300 cycle: $19140|
|500 cycle: $6380|
NovaSeq X Plus Lane Pricing
|10B: ~2.5 billion reads per lane|
|2 x 50 bp: $1100|
|2 x 100bp: $1300|
|2 x 150bp: $1400|
High Throughput Sequencing gives you options…
We offer free consultation. Please contact David Mohr to discuss your project in detail.
We offer simple, per lane and per flow cell pricing, along with end to end service for whole exome/custom targeted projects, RNASeq, and whole genome.
For NovaSeq 6000 lane loading, we now offer single lane loading on NovaSeq SP to accommodate users who do not need the throughput of a full flowcell.
For NovaSeq runs, please submit at least 50ul of your sample at 4nM.
Samples should be pooled.
Nanodrop is not reliable. Intercalating dye methods or qPCR are preferred.
Please submit 10μl of your sample at 2nM for MiSeq.
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.
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.
There are a host of options for lower input/lower quality that may add cost.
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.
Uniform Base Composition
Libraries that have uneven base composition tend to pose problems with the analysis software. These issues can be mitigated using several strategies, but the net effect will be lower data yield than a balanced library.
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 NovaSeq6000 Specification page for current data yields. While we regularly achieve greater than ‘spec’ yields from the NovaSeq6000, it is best to be conservative when planning your experiments.
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.