Support

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.

Data File Formats

This document describes the directory structure and file formats for Complete Genomics sequencing data.

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Release Notes

Describes new features and enhancements in the current release of Complete Genomics assembly pipeline.

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Getting Started Guide: First Look at CGI Genome Data

This 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.

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Annotation Tutorial

A guide to interpreting biological annotation and functional impact of Complete Genomics small variations data.

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Copy Number Variation Methods

This document provides the algorithmic details and data processing steps behind our read-depth based CNV analysis pipeline.

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Technology White Paper

Overview of Complete Genomics approach, sequencing technology, data analysis and software.

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Reanalysis Instructions

This document provides detailed instructions on how to use the Complete Genomics Reanalysis Service.

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This page contains links to the most current supporting documentation for Complete Genomics service offerings.

Specification Sheet

This document summarizes Complete Genomics Analysis Service (CGA™ Service).  CGA Service Advantages include:

  • 'Research-ready' data
  • High coverabe, accurate human genome data and analysis
  • Affordable for all study sizes
  • Simple. Fast. Complete.

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Data Deliverable

This document contains an overview of the data delivered for each human genome sequenced by Complete Genomics.

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QC Processes

This document describes the quality control systems and integrity checks that are an integral part of Complete Genomics human genome sequencing service.

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DNA to Data

This 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.

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CNV & SV Application Note

An overview of the general methodology used for CNV and SV detection, use cases and quality assessment.

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Reanalysis Flyer

An overview of the reanalysis service currently offered by Complete Genomics.

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CGI Service FAQ

Frequently Asked Questions about Complete Genomics' service offering.

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Managing Data FAQ

Frequently Asked Questions about how best to prepare for receiving the data.

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Small Variants FAQ

Frequently Asked Questions about the variation and evidence files.

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CNV, SV, and MEI FAQ

Frequently Asked Questions regarding CNV/SV data files and mobile element insertions results, and method.

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Sample Shipping and Acceptance Policy

This document details the following information:

  • Sample acceptance policy for DNA samples sent to Complete Genomics, Inc. (CGI)
  • Instructions on how to complete the Sample Manifest form (an Excel file)
  • Shipping instructions for sending DNA samples to CGI

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Quick Start Guide: DNA Sample Preparation

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:

  • DNA Sample Requirements
  • Common Reasons Why Samples Fail During Sample Quality Control
  • Qualities ...

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Sample Quality Control Protocol

This document provides detailed instructions on how Complete Genomics qualifies DNA samples prior to sequencing, including quantitation and gel electrophoresis.

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Questions?

 

For more information, please contact us at support@completegenomics.com

Call toll-free: 1-855-CMPLETE        (1-855-267-5383) or 1-650-943-2600.

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