Chromatin Immunoprecipitation Sequencing (CHIP-Seq)

Novocraft's team of experienced bioinformatics personnel work with customers to process all their sequencing data into

• Reference-based alignments per sample
• Comparison of CHIP results to control or to other samples
• Shortlist of genes (where annotations are available) within the neighbourhood of up-/downregulated CHIP binding sites on the genome
• Secure web browsing system along the reference genome used in the CHIP-Seq study

The analysis pipeline covers all of the above steps and employs state-of-the-art software tools for analyzing one-sample and two-sample data.