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 specific product documentation, literature, frequently asked questions, and documentation on sample submission.
Be sure to check back often, as we update and add to this section frequently.
This page contains links to the most current technical product documentation for Complete Genomics service offerings.
This document describes the directory structure and file formats for Complete Genomics sequencing data.
>> read moreDescribes new features and enhancements in the current release of Complete Genomics assembly pipeline.
>> read moreThis document describes Complete Genomics data in terms of the general biological trends observed in typical genomes. It provides examples, summary statistics, and metrics to help you understand what you should expect to see when you look at your sequenced genome data.
>> read moreA guide to interpreting biological annotation and functional impact of Complete Genomics small variations data.
>> read moreThis document provides the algorithmic details and data processing steps behind our read-depth based CNV analysis pipeline.
>> read moreOverview of Complete Genomics approach, sequencing technology, data analysis and software.
>> read moreThis document provides detailed instructions on how to use the Complete Genomics Reanalysis Service.
>> read moreThis page contains links to the most current supporting documentation for Complete Genomics service offerings.
This document summarizes Complete Genomics Analysis Service (CGA™ Service). CGA Service Advantages include:
This document contains an overview of the data delivered for each human genome sequenced by Complete Genomics.
>> read moreThis document describes the quality control systems and integrity checks that are an integral part of Complete Genomics human genome sequencing service.
>> read moreThis document describes Complete Genomics, Inc. (CGI) best practices on security for handling sample information and data. It includes information and details on how CGI identifies and tracks samples and resulting data.
>> read moreAn overview of the general methodology used for CNV and SV detection, use cases and quality assessment.
>> read moreAn overview of the reanalysis service currently offered by Complete Genomics.
>> read moreFrequently Asked Questions about how best to prepare for receiving the data.
>> read moreFrequently Asked Questions regarding CNV/SV data files and mobile element insertions results, and method.
>> read moreThis document details the following information:
The purpose of this guide is to list suggestions on how to provide the highest quality input DNA, ensuring the highest possible quality in genome sequence results. This quick start guide includes the following sections:
This document provides detailed instructions on how Complete Genomics qualifies DNA samples prior to sequencing, including quantitation and gel electrophoresis.
>> read more