NanoString

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nCounter System
[[image:|frame|center|200px|nCounter System (NanoString)]]

ChIP-Sequencing (or ChIP-Seq) combines chromatin immunoprecipitation (ChIP) with DNA sequencing allowing researchers to identify the binding sites of DNA-associated proteins. a

Please see below for further details about the service.

Sample Submission Guidelines

Users are required to prepare their own sequencing libraries. Samples should be gel-purified and provided UNDILUTED in EB.

Users should submit 5uL of undiluted sample. We will determine the concentration by RT-PCR and make the appropriate dilutions. Excess sample will be retained in our freezers for potential future re-run. Users are also strongly encouraged to retain a portion of their samples in case of emergency.

GTC will provide sequencing primers for libraries prepared with standard Illumina adapters. If custom sequencing primers are required they must be provided at the time of sample submission.

Data

Images acquired from the solexa sequencer are processed through the bundled solexa inage extraction pipeline to get the sequence and quality score for each base. The data is aligned to a reference genome, if requested, using an interative ELAND algorithm. An in-depth QC report is included in the package. Sample QC report is here.

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Turnaround Time

Wait times vary but are generally two weeks or less.

Pricing

Item Unit Price Per Unit Notes
Sequencing - 36 bp Single Read Sample ~$850 Cluster, Sequence, Pipeline
Sequencing - 36 bp Paired-End Reads Sample ~$1,500 Cluster, Sequence, Pipeline
Sample prep - ChIP Seq Sample Inquire -
Genome Alignment and other analysis Sample Inquire -