Next Generation Sequencing High Throughput Sequencing Services Powered By Roche GS FLX/FLX++ Roche GS Junior Illumina MiSeq Illumina HiSeq 2500 PacBio RS NGS Favourites – Straightforward Solutions 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. Feel Free To Contact Us Blog: http://ngs-expert.com Phone: +49 8092 8289-77 Official Business Hours: 8 a.m. – 6 p.m. CET eurofinsgenomics.com Toll Free Phone Austria Belgium Denmark Finland France Ireland Italy Luxemburg Numbers: 0800 296 562 0800 77862 8088 1262 0800 112 744 0800 903 807 1800 555 056 800 785 950 8002 6418 Netherlands Norway Sweden Switzerland UK 0800 0226215 800 138 44 020 798 148 0800 562 013 0800 0323 135 2013_0404/4_2013/1.000 Email: genseq-eu@eurofins.com