ChIP-Seq

ChIP Sequencing

Human whole genome sequencing enables researchers to catalog the genetic constitution of individuals and capture all the variants present in a single assay. It is applied to the study of cancer and a variety of diseases, as well as human population evolution studies and pharmacogenomics.

Overview of Service:

1. 
   State-of-the-art NGS technologies:
   350 bp insert DNA libraries
   HiSeq X platform, paired-end 150 bp
   Highest data quality:We guarantee a Q30 score ≥ 80%, exceeding Illumina’s official guarantee of ≥75%.
   Bioinformatics analysis:
   Data quality control
   Alignment with reference genome, statistics of sequencing depth and coverage
   SNP/InDel, SV and CNV calling, annotation and statistics
   Somatic SNP/InDel, SV and CNV calling, annotation and statistics for tumor-normal paired samples.
   Fast turnaround time:
   20 working days after verification of sample quality (without data analysis)
   Additional 8 working days for data analysis
   Recommended Sequencing Depth

   For tumor tissues: 50×, adjacent normal tissues and blood 30×
   For rare diseases: 30~50x.