Next generation sequencing
Roche / 454 Genome Sequencer FLX
+ Titanium
Deep sequencing up to 1000 bp read
length and up to 1.1 Gb / run
- De novo sequencing by whole shotgun approach and
closure of gaps using paired-end applications and Sanger
sequencing
- Re-sequencing and comparative genomics including sequence
assembly and mapping to a reference genome
- Transcriptome analysis by generating standard or normalised
full length optimised cDNA libraries
- Metagenome analysis by sequencing the whole genomic content or
16S rDNA in a complex sample (high specificity due to long read
length; sorting and clustering of reads)
- Amplicon sequencing and analysis of variants (SNPs) using
state-of-the-art analysis tools (e.g. Roche GS Amplicon Variant
Analyzer)
- Sequencing of tagged fosmids / BACs
- ChIP-sequencing
- DNA methylation analysis
Roche / 454 Genome Sequencer FLX + Titanium
Contact
us:
Infoline: +49 (0) 30 5304 2260
Email: ngs@lgcgenomics.com
For an overview of our NGS services click here