C++ library and its applications to generate and process accurate consensus sequences
- Getting Started
- Projects
- Available
- Planned
- Genomic Consensus Calling
gcpp
- Viral Haplotype Phasing
eden
- Genomic Consensus Calling
- 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.
juliet
identifies minor variants from aligned ccs reads.
fuse
reduces an alignment into its closest representative sequence.
cleric
swaps the reference of an alignment by transitive alignment.
julietflow
automatizes the minor variant pipeline.
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.