Short-read (Illumina) Library Construction Services

Introduction

Genomic DNA libraries with different-sized inserts
RNA-seq libraries with w. Poly-A enrichment,strand-specific
RNA-seq libraries with Ribo-depletion,strand-specific
3′-Tag-Seq RNA-seq for gene expression profiling
High-Throughput (HT) library preps (DNA or RNA; starting from 24 libraries; please see below)
miRNA-seq libraries (microRNA)
Mate-Pair libraries
10X-Genomics GemCode (“linked-read”) libraries
Exome capture
ChIP-seq
Methyl-Seq: WGBS (Whole Genome Bisulfite Seq) and RRBS (Reduced Representation Bisulfite Seq)
Reduced Representation libraries (e.g. for Genotyping By Sequencing (GBS) applications)
PCR-free libraries
BluePippin library size selection

Summary

Our library preparation services include library QC, library quantification, and library pooling. All our libraries are indexed (have a barcode). We use UDI barcodes (unique -dual-indexing) wherever the protocol allows.
We are happy to discuss the options and protocols suitable for your specific research projects. We prepare standard sequencing libraries as well as many specialized libraries and can also help you with custom projects.

CD Genomics has already updated its technology platforms to mainstream NGS, long-read sequencing, and microarray instruments. We continue to strive to offer the same reliable services to pharmaceutical and biotechnology companies, as well as academia and government agencies, for all your sequencing or array needs. If you are interested, please contact us directly for assistance.