Complete Genomics is committed to supporting our customers. Part of our commitment to helping you includes providing informational resources for download. Here you’ll find documentation for each step of your project.
Sample Preparation
• Sample Submission Instructions
• Sample Quality Control Protocol
Sequencing
• Complete Genomics Service FAQ
• Application Note: To Get the Whole Picture, Sequence the Whole Genome
• Case Study: Miller Syndrome Family Study
• Publication: Human Genome Sequencing Using Unchained Base Reads on Self-assembling DNA Nanoarrays
Data and Methods
• Standard Sequencing Service – Getting Started Guide
• Cancer Sequencing Service – Getting Started Guide
• Copy Number Variation Methods
• Small Variant Assembler Methods
• Lesser Allele Fraction Methods
• Publication: Computational Techniques for Human Genome Resequencing Using Mated Gapped Reads
Data Management
• DNA to Data Security Product Note
Downstream Analysis
• Complete Genomics Tool Repository