The GenomicConsensus
package provides the quiver
tool, PacBio's flagship consensus
and variant caller. The backend logic is provided by the
ConsensusCore
library, which you must install first.
Make sure you have set up and activated your virtualenv, and
installed pbcore
and ConsensusCore
(which cannot be
installed automatically by pip or setuptools). Then:
% python setup.py install
Basic usage is as follows:
% quiver aligned_reads.cmp.h5 -r reference.fasta -o variants.gff -o consensus.fasta -o consensus.fastq
in this example we perform haploid consensus and variant calling on the mapped reads in the aligned_reads.cmp.h5
which was aligned to reference.fasta
. The reference.fasta
is only used for designating variant calls, not for computing the consensus. The consensus quality score for every position can be found in the output FASTQ file.