General

• How long does genome sequencing take?
• How long will you store my sample or extraction?
• Sample Submission and Shipping Guidelines
• What does your pricing include?
• What is The Sequencing Center's biosafety rating?

Genome Sequencing

• Can you run custom gene panels?
• Group or Crowd Sequencing
• How do you quantify DNA concentration?
• Trimming Illumina adapter sequences
• Types of Genome Sequencing
• What are paired-end reads?
• What is multiplexing?
• What organisms can you sequence?

HLA Typing

• GenDx HLA Publication List
• HLA IMGT Database Update
• HLA Nomenclature
• HLA Typing Sample Requirements
• HLA Update
• How to access your sequencing data
• How to read HLA reports
• What's included in "basic bioinformatics"?

Whole Genome Bioinformatics

• Can I use one of my sequenced samples as a reference genome?
• Coverage
• De novo assembly
• FastQ Files
• Geneious Sequence Alignment & Variant Calls Workflow
• Geneious Variant Call Reports
• How to access your sequencing data
• Phaster for Bacteriophage Data Analysis
• Reference Genomes
• Sequence Alignments with Geneious
• Trimming Illumina adapter sequences
• What Are Unmapped Reads?
• What is multiplexing?
• What's included in "basic bioinformatics"?
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Metagenomic Bioinformatics

• How to access your sequencing data
• Microbiome Reports with Kraken
• Microbiome Reports with Megan6
• Microbiome Reports with One Codex
• Trimming Illumina adapter sequences
• What is multiplexing?
• What's included in "basic bioinformatics"?

Documentation

• Documents