C++ library and its applications to generate and process accurate consensus sequences
- Getting Started
- Projects
- Available
- Consensus Core
- Circular Consensus Calling
ccs
- Work in Progress
- Genomic Consensus Calling
gcpp
- Viral Haplotype Phasing
eden
- Genomic Consensus Calling
- Planned
- Minor Variant Calling
- Available
- Developer environment
- PacBio open source license
ccs
takes multiple reads of the same SMRTbell sequence and combines
them, employing a statistical model, to produce one high quality consensus sequence.
gcpp
will replace the current python GenomicConsensus, until then please use the existing solution.
This tool will be able to precisely call single-nucleotide variants from consensus data.
eden
will leverage CCS reads to identify low-frequency haplotypes within polyploid samples.
Support is only provided for official and stable SMRT Analysis builds provided by PacBio and not for source builds.