Penn Genomics Analysis Core
Sanger sequencing, genotyping and fragment sizing.
What they do
- Services
- Sanger sequencing
- Genotyping
- Fragment sizing
- High throughput sequencing
- Plasmid DNA preparation
- FASTA conversion
- Primer walking
- Deletion subcloning
- Sequence assembly
- ORF analysis
- Homology searches
- Data analysis service
- DNA/RNA quantification
- DNA fragment size selection
- DNA/RNA visualization
- Targeting vector construction
- Southern blotting probes
- Construct DNA purification
- Capillary electrophoresis
- Sanger’s dideoxy Terminator Method
- Ion Torrent sequencing
- AmpliSeq technology
- Multiplex PCR
- BAC recombineering
- Cre recombinases
- Flpe recombinases
- Qubit 2.0 fluorometry
- Pippin Prep
- RNA 6000 Pico assay
- RNA 6000 Nano assay
- DNA 1000 assay
- DNA High Sensitivity assay
- S5 sequencing
- Human exome sequencing
- Whole RNA-seq
- Targeted gene panels
- Bacterial genome sequencing
- Viral genome sequencing
- Variant calling
- Differential gene expression
- Alternative splicing identification
- S5 run throughput
- 3730XL sequencing
- Read length over 700 bases
- Rapid turnaround