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Documentation

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.

Be sure to check back often, as we update and add to this section frequently.

Sample Preparation

Sample Preparation FAQ

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

Overview of Data Delivered

Standard Sequencing Service - Getting Started Guide

Cancer Sequencing Service - Getting Started Guide

Data File Formats

Copy Number Variation Methods

Small Variant Assembler Methods

Lesser Allele Fraction Methods

CNV, SV, MEI FAQ

Small Variants FAQ

Publication: Computational Techniques for Human Genome Resequencing Using Mated Gapped Reads

Small Variant Score Calibration Methods

Data Management

DNA to Data Security Product Note

Managing Data FAQ

Downstream Analysis

Complete Genomics Tool Repository

Reanalysis

Reanalysis Service

Reanalysis Instructions

Public Data Information

Public Genome Data Repository Service Note

Questions?

For sales inquiries please contact info@completegenomics.com

For support please visit our Technical Support page.

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