Payment & Shipping Terms:
|Sample-1:||Fresh Cell Or Issue||Sample-2:||DNA 1～2 μg, >20 Ng/μl|
|Sample-3:||RNA ≥2μg, >750ng/μl||Report:||QC Report|
|Electronic Data:||Sequencing And Figure||Turnaround:||3 Months|
2μg RNA NGS Next Generation Sequencing,
2 μg DNA NGS Next Generation Sequencing,
Fresh Cell NGS Next Generation Sequencing
High-throughput sequencing is a cutting-edge tool for quantitative trait gene (QTG) cloning, which is dependent on the mutant gene map of a large-scale segregation population as the clone complex trait.High-throughput sequencing methods generate large amounts of sequence data and require robust computational tools for further analysis. CELLFREE provides algorithms to support common analysis workflows for Next-Generation Sequencing (NGS) data, such as filtering and trimming reads, mapping reads to references, counting the number of reads mapped to genomic features, and performing statistical analyses.
Our services include capture chip preparation, library preparation, sample validation, as well as sequencing and bioinformatics analysis.