PacBio Sequel
Features
Long Reads: With reads tens of kilobases in length you can readily assemble complete genomes and sequence full-length transcripts
High Accuracy: Sequencing free of systematic error achieves >99.999% consensus accuracy? Uniform Coverage: No bias based on GC content means you can sequence through regions inaccessible to other technologies
Single-Molecule Resolution: Capturing sequence data from native DNA or RNA molecules enables highly accurate long reads with >99% single-molecule accuracy
Epigenetics: With no PCR amplification step, base modifications are directly detected during sequencing
Applications
Whole Genome Sequencing
Full Length Transcriptome Sequencing
Metagenome Sequencing
16S rDNA Full Length Sequencing
Organelle genome sequencing
Whole Genome Resequencing & Rare Variation Identification
Epigenetics
