Viral / Molecular Core High Density Sequencing Support
High density sequencing is an emerging technology with the capacity to generate millions of sequences, with up to a billion bases of sequence in a single run. This approach is ideal for characterizing complex populations such as HIV and SIV, HBV/HCV, and sites of retroviral DNA integration.
The Viral/Molecular Core is now offering Illumina sequencing as a service. In each case, amplicons will be generated from samples of interest, then sample sequences determined. Sequences are subject to stringent quality control algorithim and provided to users in fasta format. Bioinformatic analysis is available on a fee-for-service basis. The core also provides advice on experimental design, sequence work up, statistical analysis, and long term data storage.
Several services are offered.
- Initial consultation on experimental design (free of charge)
- Deep sequencing of viral genomes
- Sequencing of sites of retroviral DNA integration
- Programmer time for data analysis
The Core provides support for each of these areas through the expertise of Dr. Frederic Bushman (Core Co-Director). Advanced bioanalytic support and analysis is offered collaboratively through the Biostatistics and Data Management Core (Core G) by Dr. Hongzhe Li (Core G Co-Investigator).
For further information on utilizing V/M Core support for high density sequencing, contact Aubrey Bailey.
Order High Density Sequencing services through the Path BioResource at Penn. Instructions for the Path BioResource can be found here on the CFAR website or on the Path BioResource site itself.
Core Service Contact:
Viral and Molecular Core
Programmer time is available to support several Core activities. Programmer time is available to implement bioinformatic pipelines for analyzing deep sequencing data on populations on viral genomes or integration sites. Support is also available for management of deep sequencing data. Services include data and metadata housing, storage, back-up and sequence uploads to national archives such as NCBI-SRA (which is required for publication of sequence data).