BioMicroCenter:Singular Sequencing: Difference between revisions
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Compared to a typical Illumina library, a Singular index 1 would be the reverse compliment of the i5 index, whereas index 2 would be the reverse compliment of the i7 index. | |||
===Lane-by-lane Requirements=== | |||
*Must be 50 or 150 paired-end dual indexed | |||
*Pool must be compatible with TruSeq, Nextera, TruSeq, smRNA and Solexa sequencing primers | |||
Minimum reads per lane are guaranteed if: | Minimum reads per lane are guaranteed if: | ||
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*submitted libraries are at least 2 nM. | *submitted libraries are at least 2 nM. | ||
All other requests, including use of custom sequencing primers require a full flowcell. Illumina libraries which have been converted in the Center will also require a full flowcell. | |||
*Min custom primer submission: 20 uL at 100 uM | |||
[[IMAGE:IndexhopF3.jpeg|left|250px|Index hopping for a standard set of Singular libraries]] [[IMAGE:PPPPF3.jpeg|right|200px|Percent Perfect Plot for Singular libraries 150PE]] | |||
Index hopping on Singular runs has been low. The performance of an F3 flowcell mimics other short-read 4 color chemistry sequencers with patterned flowcells. | |||
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== The G4 Platform == | == The G4 Platform == |
Latest revision as of 17:26, 9 June 2025
Singular Sequencing[edit]
The Center currently hosts a G4 platform by Singular Genomics. Singular’s G4 platform is a short-read mid-throughput sequencing platform delivering adequate sequencing data through its proprietary sequencing-by-synthesis chemistry at a significantly competitive price point.
Service | Singular Sequencing |
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INPUT | Singular libraries |
MIN VOLUME | 12 uL |
MIN CONCENTRATION | 4 nM |
INCLUDED SERVICES |
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ADDITIONAL SERVICES |
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DATA FORMATS |
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QUALITY CONTROL |
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PRICING | LINK |
SUBMISSION |
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Compared to a typical Illumina library, a Singular index 1 would be the reverse compliment of the i5 index, whereas index 2 would be the reverse compliment of the i7 index.
Lane-by-lane Requirements[edit]
- Must be 50 or 150 paired-end dual indexed
- Pool must be compatible with TruSeq, Nextera, TruSeq, smRNA and Solexa sequencing primers
Minimum reads per lane are guaranteed if:
- the BMC has performed quality control,
- the samples are high-complexity, especially for the first 10 nt of read 1, and
- submitted libraries are at least 2 nM.
All other requests, including use of custom sequencing primers require a full flowcell. Illumina libraries which have been converted in the Center will also require a full flowcell.
- Min custom primer submission: 20 uL at 100 uM


Index hopping on Singular runs has been low. The performance of an F3 flowcell mimics other short-read 4 color chemistry sequencers with patterned flowcells.