PCR
PCR is capable of replicating DNA fragments millions of times over. We use PCR to identify infections more precisely and to detect disease and genetic mutations. It is a sensitive and reliable process that remains a critical tool in diagnostic medicine and related research.
1–3 hours
Run time
Targeted
Method type
6–48 hours
Run time
High
Flexibility
NGS
NGS is used to quickly read and process large DNA and RNA datasets and is capable of identifying genetic mutations and patterns with exceptional accuracy and speed. In the field of genomics, the value of PCR is unparalleled, as it supports research, diagnosis, and the development of targeted treatments for cancer and other diseases.
PCR vs NGS Comparison
Feature |
PCR |
NGS |
| Throughput | Low to medium | Very high |
| Data Type | Targeted sequences | Whole genome/transcriptome |
| Run Time | 1–3 hours | 6–48 hours |
| Flexibility | Limited to specific targets | Broad genomic coverage |
| Applications | Diagnostics, mutation detection | Genomics, precision medicine |
Feature
Throughput
Data Type
Run Time
Flexibility
Applications
PCR
Low to medium
Targeted sequences
1–3 hours
Limited to specific targets
Diagnostics, mutation detection
NGS
Very high
Whole genome/transcriptome
6–48 hours
Broad genomic coverage
Genomics, precision medicine
If you are unsure which methodology is most appropriate for your study, we invite you to engage with our experts. We will work closely with you to understand your study goals and expectations and support you in making the best possible decision to support your success.
At US Biolab, we are dedicated to advancing biomedical discovery by providing access to ethically sourced, clinically annotated human biospecimens.
Compliance
IRB-approved, ethically sourced specimens
Quality Assurance
Pathology reports & clinical data available
Global Access
Samples shipped worldwide in compliance with regulations
Scientific Support
Speak with our biospecimen specialists for custom requests