Functional Genomics Core - Next-Gen Sequencing

Illumina's High-Throughput Sequencers offers us a unique opportunity to expand our service far beyond what can currently be achieved using traditional hybridization based approaches to analyze both expression and promoter occupancy studies. The traditional tools for this type of analysis are limited by the number of probes that can be spotted onto an array and by limited detection sensitivity and dynamic range. The sequencers create a unique opportunity for investigators to generate datasets that will go far beyond these limits, as the system in simplest terms counts molecules of DNA, allowing investigators to detect single copy genes and entirely novel transcripts or regulatory regions for which traditional array probes do not exist. Furthermore, the Illumina® Sequencing by Synthesis technology employed by the system allows investigation of RNA or DNA from any species, and will allow investigation of species for which traditional arrays do not exist. This system can be utilized by researchers with interests in gene expression analysis, Whole-Genome Chromatin IP Sequencing (ChIP-Seq), DNA methylation studies, SNP analysis, micro RNA analysis, gene discovery and sequencing. The numerous application and power of this system will give DERC/IDOM and Penn researchers a significant advantage in their field of study and enable them to publish in high impact journals.


Genome Analyzer IIx

Using a massively parallel sequencing approach, the Illumina® Whole Genome Analyzer IIx can generate more than one billion bases of data in a single run or 45 million uniquely aligned reads per lane. The system leverages Illumina's sequencing technology and novel reversible terminator chemistry, optimized to achieve unprecedented levels of cost effectiveness and throughput.


HiSeq 2000

The HiSeq 2000 sequencing system offers unprecedented output and a breakthrough user experience. HiSeq 2000 delivers the industry's highest sequencing output and fastest data generation rate. The HiSeq allows us to be more flexible in scheduling our 100bp PE runs and be able to accommodate our collaborators needs. Currently, the HiSeq generates around 300 billion bases per flowcell and over 200 million uniquely aligned reads per lane.

...........................................................................................................................................................................................

© Trustees of the University of Pennsylvania

FGC HOME

Core Information


Microarray Information

Next-Gen Sequencing

Advanced Analysis

Sample Quality

Other Services

Workflow

Experiment Submission

Staff

Links


GLITR

TessLA

Sample Queue

Jonathan's Calender

Request Advanced Analysis

Kaestner Lab Website

Documents


RNA Extraction Protocol

ChIP Protocol

ChIP-Seq Protocol

Publications