Sampler NGS Service
Looking to use NGS to advance in your project but wish to run a trial study first without spending too much? 1st BASE Sampler NGS Service can provide you with that option; our lane, library, and platform based prices have enabled unbeatable savings in this new service initiative.
By consolidating bulk samples and streamlining data analysis, we are able to pass on the savings to you so you have the option of paying much less if you have time to spare and require only basic data analysis.
You can also choose to fast-forward your entire project at any point by upgrading to our premium NGS Concierge Service
Features
- Suitable for NGS studies
- Flexibility of deciding how many units required reduces excess reads
- Consolidation of samples allow cost-savings
- 2 months maximum hold period before all samples will be processed
- Inclusive of 1 basic bioinformatics data analysis option
Specifications
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Platform
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Sequencing approach
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Format
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Data Output
(Not guaranteed in Sampler NGS)
|
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Roche-454
GS-FLX Titanium
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1x ~400b
Single-End (shotgun)
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1 sample,
1/8 PTP region
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80,000 to 120,000 reads, 30 to 55 Mb
|
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Multiplexed (barcoded),
1 sample out of 12,
1/8 PTP region
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6,000 to 10,000 reads, 2 to 4 Mb
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Illumina
HiSeq 2000
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2x100b
Paired End
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1 sample,
1 lane (channel)
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120 million reads
(60 million paired reads), 12 Gb
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Multiplexed (indexed),
1 sample out of 12,
1 lane (channel)
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10 million reads
(5 million paired reads), 1 Gb
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Life Technologies ABI SOLiD 4
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1x50b
Single End
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1 sample,
1 quad region (1/4 slide)
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65 to 85 million reads, 3 to 4 Gb
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Multiplexed (barcoded),
1 sample out of 12,
1 quad region (1/4 slide)
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5.4 to 7 million reads, 270 to 350 Mb
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Payment
A 50% down payment is required before commencement of project.
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