The NovaSeqTM X Plus instrument employs the same general principles for sequencing libraries of short DNA molecules as the NovaSeqTM 6000 instrument. However, there are differences in the sequencing chemistry (e.g., modified nucleotides, polymerases) and the image acquisition system. These could impact the obtained sequencing data.
We conducted several tests with different datasets and specifications to show that the sequencing results are comparable between the NovaSeqTM X Plus and the NovaSeqTM 6000. Subsequently, we compared the sequencing data with the following results:
- The NovaSeqTM X Plus instrument has a lower reported error rate than the NovaSeqTM 6000 instrument.
- The NovaSeqTM X Plus instrument does not introduce sequencing errors that negatively affect the sensitivity and precision of variant calling compared to the NovaSeqTM 6000 instrument.
- No difference can be detected between the sequence error profiles of the NovaSeqTM X Plus instrument and the NovaSeqTM 6000 instrument.
The NovaSeqTM X Plus instrument does not add bias due to sequence or GC content. Read sequences accurately reflect the molecular sequences in the libraries, allowing for highly accurate variant calling. Overall, the NovaSeqTM X Plus sequencer can replace the currently used NovaSeqTM 6000 instrument from a technical point of view.
Find here more information about the sequencing technologies used by CeGaT