The Next-Generation Sequencing Core offers comprehensive high-throughput sequencing services from experiment design to basic data analysis to members of the University of Pennsylvania
Frequently Asked Questions
- Is this the sequencing core I want?
- What does it cost?
- How do I get started?
- Selecting BARCODES
- How do I make *-Seq libraries?
- Does the NGSC make *-Seq libraries?
- When can I bring my samples in?
- How are my samples doing?
- How do I download data?
- Where is my old data?
- Where is the old TessLA browser?
seqeuencing-queue from trello
Services Offered by the FGC
|Experiment Design||Advice on techniques, sequencing depth, and analysis.|
|Microarrays||Agilent microarrays for RNA expression experiments.|
|Sample Quality Assessments||Agilent bioAnalyzer and TapeStation, *** quBit|
|Library Preparation||Various protocols for Illumina sequencing.|
|Illumina hiSeq sequencing||50bp and 100bp, single-read and paired-end|
|Illumina miSeq sequencing||50 to 500bp total, single-read and paired-end|
|Data Analysis||Basic and custom analysis for microarray and sequencing data.|