Next generation sequencing
Illumina HiSeq 2000
Up to 3 billion reads per flow cell and up
to 300 Gb per flow cell
- Genome sequencing and re-sequencing to
discover SNPs and chromosomal rearrangements
- Transcriptome analysis, generation of
expression profiles, detection of splice variants etc.
- Small RNA / microRNA discovery and
analysis
- ChIP-seq application resulting in the
identification and quantification of protein-DNA interactions
- DNA methylation analysis to discover
methylation variable positions across the whole genome.
Illumina HiSeq 2000
Contact us:
Infoline: +49 (0) 30 5304 2260
Email: ngs@lgcgenomics.com
For an overview of our NGS services click here