Illumina sequencers available at NSC
MiSeq (Link to Illumina specs: Miseq)
Applications: Small genome DNA sequencing (de novo & resequencing); Metagenomics studies (including rDNA); Amplicon sequencing; Targeted resequencing, such as gene panels; Control of libraries for large projects; smallRNA/microRNA sequencing; Epigenetic studies with few samples
Sequencer | Read length | Output per run | NSC guarantee | |
reads per end (M) | Bases (Gb) | reads per end (M) | ||
MiSeq v3 | 75 PE | 22 - 25 | 3.3 - 3.8 | 10* |
300 PE | 13 - 15 | |||
Miseq v2 |
50 SR |
12 - 15 | 0.7 - 0.8 | 6* |
25 PE | 0.7 - 0.8 | |||
150 PE | 4.5 - 5.1 | |||
250 PE | 7.5 - 8.5 | |||
MiSeq v2 micro | 150 PE | 4 | 1.2 | 2* |
MiSeq v2 nano | 150 PE | 1 | 0.3 | 0.5* |
250 PE | 0.5 |
NextSeq 500 (Link to Illumina specs: NextSeq)
Applications: Genomic DNA sequencing; Exome sequencing; mRNA sequencing; smallRNA/microRNA sequencing; Epigenetics: Chromatin immunoprecipitation sequencing; DNA methylation; Small genome DNA sequencing (de novo & resequencing); Targeted resequencing, such as gene panels
Sequencer | Read length | Output per run | NSC guarantee | |
reads per end (M) | Bases (Gb) | reads per end (M) | ||
NextSeq High Output |
75 SE | 400 | 25 - 30 | 200* |
75 PE | 50 - 60 | |||
150 PE | 100 - 120 | |||
NextSeq Mid Output |
75 PE | 130 | 16 - 19 | 65* |
150 PE | 32 - 39 |
HiSeq 3/4000 & HiSeq X (Link to Illumina specs: HiSeq 3/4000, HiSeqX) Each run contains 8 separate lanes
Applications: Genomic DNA sequencing (the only application for HiseqX); Exome sequencing; mRNA sequencing; smallRNA/microRNA sequencing; Epigenetics: Chromatin immunoprecipitation sequencing, DNA methylation
Sequencer | Read length | Output per run | NSC guarantee | |
reads per end (M) |
Bases (Gb) | reads per end (M) | ||
HiSeq 3/4000 | 50 SE | 2500 | 105 - 125 | 1250* |
75 PE | 325 - 375 | |||
150 PE | 650 - 750 | |||
HiSeq X | 150 PE |
5300 - 6000 |
800 - 900 | 2500* |
NovaSeq (Link to Illumina specs: NovaSeq)
With NovaSeq Xp reagents, we can separate the SP, S1 and S2 flow cells into 2 separate lanes, S4- into 4 lanes. We will run half or quarter flow cells only when we have enough other projects to fill the flow cell (longer queue times).
Applications: Genomic DNA sequencing; Metagenomics; Exome sequencing; mRNA sequencing; smallRNA/microRNA sequencing; Epigenetics: Chromatin immunoprecipitation sequencing, DNA methylation
Sequencer | Read length | Output per run | NSC guarantee | |
reads per end (M) | Bases (Gb) | reads per end (M) | ||
NovaSeq SP | 50 PE | 650 - 800 | 65 - 80 | 400* |
100 PE | 134 - 167 | |||
150 PE | 200 - 250 | |||
250 PE | 325 - 400 | |||
NovaSeq S1 |
50 PE |
1300 - 1600 | 134 - 167 | 800* |
100 PE | 266 - 333 | |||
150 PE | 400 - 500 | |||
NovaSeq S2 | 50 PE | 3300 - 4100 | 333 - 417 | 2000* |
100 PE | 667 - 833 | |||
150 PE | 1000 - 1250 | |||
NovaSeq S4 | 100 PE | 8000 - 10 000 | 1600 - 2000 | 5000* |
150 PE | 2400 - 3000 |
Data output performance guarantees
If your samples are submitted in accordance with these guidelines and meet our quality and quantity requirements, we provide the performance guarantees given in the table. Note that these are our minimal output criteria and we routinely expect greater output. Should we fail to meet these targets, we will run additional sequencing at no cost to you or offer a discount as appropriate. In the case of multiplexed samples, we cannot guarantee equal distribution of reads between different indexes, but we do run a qPCR assay to achieve this as best possible.
*Exceptions: Data guarantees are not valid for long-insert libraries (insert size > 500 bp) and low-diversity samples (e.g. PCR amplicons, restriction digestion fragments, RAD libraries), which require dilution and blending with control library using Illumina technology.
Note that if your submitted samples do not meet our quality or quantity criteria, we may still be willing to attempt sample prep and sequencing, but our performance guarantee no longer applies and you will be liable for all expenses incurred regardless of the output amount, also in the event that no sequence data can be generated.