In this guide, we define sequencing coverage as the number of unique reads that include a given nucleotide in the target region or genome of interest. Coverage and read requirements can depend on several of the following parameters:
• Application type
• Genome size, or in the case of target enrichment, region of interest/capture design size
• Genome complexity
• Read length
• Sequencing error rate
• Bioinformatics pipeline
Note
If you need more guidance regarding depth of coverage, contact Customer Care for consultation.