Services
Next generation sequencing
The new Illumina HiSeq 2000 sequencing
platform together with the Roche / 454 GS FLX + Titanium
and the state-of-the-art ABI 3730xl technologies allow
LGC Genomics to offer the whole range of Next Generation Sequencing
services covering various application areas.
Please click
here to download a summary of our NGS services
information.
- De novo sequencing including
gap closure
(of prokaryotic and eukaryotic genomes
using Roche / 454, Illumina HiSeq 2000 and Sanger sequencing as
well as other state-of-the-art techniques)
- Re-sequencing of
genomes
- Transcriptome sequencing and
analysis
(of eukaryotic and prokaryotic
organisms)
- Metagenome sequencing and
analysis
- Analysis of:
-
methylation patterns
- amplicons (e.g. 16S rDNA)
- pools of tagged fosmids / BACs
- ChIP and small RNA
sequencing
Special customised
applications:
- Targeted
re-sequencing
(re-sequencing of enriched individual
genomic regions of interest e.g. exomes, chromosomal intervals
etc.)
- Sample multiplexing
- Sequence enrichment
Contact us:
Infoline: +49 (0) 30 5304
2260
Email: ngs@lgcgenomics.com
For more information about NGS services using
different platforms please click below:
Next generation sequencing services by
LGC Genomics include:
- Extensive consultation and experiment design
assistance by our experienced scientific staff.
Bioinformatic services
- De novo assembly of genomes
- Mapping to reference genomes
- Sorting of tagged sequences
- Metagenomics data analysis
- SNP analysis of amplicons
- Clustering of transcripts
- Various sequence alignment procedures
- Clipping of adaptors, linkers etc.
Expertise
- Publicaton quality sequencing of
bacterial and fungal genomes
- Development of a novel method to sequence
complete transcriptomes starting from normalised
full length optimised cDNA libraries. Our method yields balanced
transcriptome sequences without the usual 3' or 5'
biases.
- Vast experience in sequencing
metagenomes from various habitats
A reference list can be provided upon request.