Next Generation Sequencing
High Throughput Sequencing
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Roche GS Junior
Illumina MiSeq
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NGS Favourites –
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For Complex Projects
eurofinsgenomics.com
De Novo Sequencing of Genomes
Re-Sequencing of Genomes and
Comparative Genomics
Transcriptome Analysis
Ultra Deep Amplicon Sequencing
Targeted Re-Sequencing by
Sequence Capture
Human Data Analysis and Data Mapping
Customised Bioinformatics Services
NGS Library Generation Services
Take Advantage Of Our Most Comprehensive NGS Portfolio
Genome sequencing
De novo sequencing of viral, prokaryotic, fungal and higher eukaryotic genomes of any size - from shotgun coverage
sequencing to complete finishing and data analysis
Scaffolding of contigs by sequencing either long paired-end (LPE) libraries on GS FLX/FLX++ or long jumping distance (LJD) libraries on HiSeq or MiSeq; libraries are available with jumping distances of 3 kbp, 8 kbp, 20 kbp and/or 40 kbp, respectively
Re-sequencing of genomes of any size to analyse genetic variations
Transcriptome analysis
Sequencing of whole transcriptomes with our normalised random primed cDNA libraries
High resolution expression profiling with our 3’-fragment libraries
Sequencing of Illumina mRNA libraries and small RNA libraries on HiSeq 2000
Amplicon sequencing
Diversity screenings within populations of individuals or metagenome analysis by ultra deep sequencing on GS FLX/FLX++
Identification of rare mutations associated with disease (SNP detection) by ultra deep sequencing on GS FLX/FLX++
Sorting, clustering and comprehensive variance analysis of amplicon reads
Targeted re-sequencing by sequence capture
Any specified region – contiguous or non contiguous (e.g. exons)
Roche NimbleGen EZ Libraries for customised capture projects (human & non-human samples)
NGS library generation services
Genomic shotgun libraries to be sequenced on GS FLX/FLX++, MiSeq or HiSeq
Specialised libraries for GS FLX/FLX++ (e.g. LPE libraries) or HiSeq/MiSeq (e.g. mRNA libraries)
Bioinformatics services
All common standard solutions, like assembly, annotation, mapping and clustering service
Customised bioinformatics solutions adapted for your needs
NGS Favourites
Predesigned packages based on a best practise approach that includes all steps to successfully finalise your project
Expertise & high quality combined with attractive prices ensure premium data quality
Available for a variety of application areas (e.g. de novo genome sequencing, re-sequencing & amplicon sequencing)
GS FLX/FLX++ and GS Junior are trademarks of Roche, Illumina, MiSeq and HiSeq are trademarks of Illumina, Inc, PacBio RS is a trademark of Pacific Biosiences of California, Inc.
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2013_0404/4_2013/1.000
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