Equipment & Services

Exome sequencing is a simple, efficient method for high-confidence calling of exonic variants. The Nextera Exome Kit delivers an average of >75% of on-target sequencing reads. This high on-target percentage requires fewer sequencing cycles to reach desired coverage levels but still achieves uniform coverage for high-confidence results.

Starting from just 50ng of genomic DNA this kit uses transposase-based fragmentation and exome enrichment with biotinylated capture probes to capture coding exons covering 45 Mb of exonic content (≥98% of RefSeq, CCDS, and Ensembl coding content). Multiplexing up to 12 samples per flowcell can be achieved. As well as the raw sequence data we also supply filtered variants lists and basic bioinformatics.

Please contact us for pricing.

Chromatin immunoprecipitation (ChIP) sequencing is a powerful method for identifying genome-wide DNA binding sites for transcription factors and other proteins. Following ChIP-Seq protocols, DNA-bound protein is immunoprecipitated using a specific antibody.  The bound DNA is the coprecipitated, purified, and sequenced. 

Through examining protein-nucleic acid interactions at a genome-wide scale, ChIP-Seq reveals insights into gene regulation events involved in various diseases and biological pathways.

Small RNA sequencing is a technique to isolate and sequence small RNA species, such as miRNAs.  Small RNA-Seq can query thousands of small RNA and miRNA sequences with unprecedented sensitivity and dynamic range.

Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, etc. Multiplex up to 384 samples. Ideal for small genomes and works for any species.

Whole-transcriptome analysis with total RNA sequencing defects coding plus multiple forms of non-coding RNA.

Total RNA-Seq can accurately measure transcript abundance and identify known and novel features of the transcriptome.