com.fulcrumgenomics.umi.ReviewConsensusVariants
The chromosome on which the variant exists.
The position of the variant.
The reference allele at the position.
The genotype of the sample in question.
The set of filters applied to the variant in the VCF.
The count of A observations at the variant locus across all consensus reads.
The count of C observations at the variant locus across all consensus reads.
The count of G observations at the variant locus across all consensus reads.
The count of T observations at the variant locus across all consensus reads.
The count of N observations at the variant locus across all consensus reads.
The consensus read name for which the following fields contain values.
A description of the insert that generated the consensus read.
The base call from the consensus read.
The quality score from the consensus read.
The number of As in raw-reads contributing to the consensus base call at the variant site.
The number of Cs in raw-reads contributing to the consensus base call at the variant site.
The number of Gs in raw-reads contributing to the consensus base call at the variant site.
The number of Ts in raw-reads contributing to the consensus base call at the variant site.
The number of Ns in raw-reads contributing to the consensus base call at the variant site.
The count of A observations at the variant locus across all consensus reads.
The count of C observations at the variant locus across all consensus reads.
The count of G observations at the variant locus across all consensus reads.
The count of N observations at the variant locus across all consensus reads.
The count of T observations at the variant locus across all consensus reads.
The number of As in raw-reads contributing to the consensus base call at the variant site.
Gets the value of the field by name.
Gets the value of the field by name.
The number of Cs in raw-reads contributing to the consensus base call at the variant site.
The chromosome on which the variant exists.
The base call from the consensus read.
A description of the insert that generated the consensus read.
The quality score from the consensus read.
The consensus read name for which the following fields contain values.
The set of filters applied to the variant in the VCF.
Override this method to customize how values are formatted.
Override this method to customize how values are formatted.
The number of Gs in raw-reads contributing to the consensus base call at the variant site.
The genotype of the sample in question.
Gets the value of the field by name, returns None if it does not exist.
Gets the value of the field by name, returns None if it does not exist.
Gets an iterator over the fields of this metric in the order they were defined.
Gets an iterator over the fields of this metric in the order they were defined. Returns tuples of names and values
The number of Ns in raw-reads contributing to the consensus base call at the variant site.
Get the names of the arguments in the order they were defined.
Get the names of the arguments in the order they were defined.
The position of the variant.
The reference allele at the position.
(Changed in version 2.9.0) The behavior of scanRight
has changed. The previous behavior can be reproduced with scanRight.reverse.
The number of Ts in raw-reads contributing to the consensus base call at the variant site.
(Changed in version 2.9.0) transpose
throws an IllegalArgumentException
if collections are not uniformly sized.
Get the values of the arguments in the order they were defined.
Get the values of the arguments in the order they were defined.
(consensusVariantReviewInfo: MonadOps[(String, String)]).filter(p)
(consensusVariantReviewInfo: MonadOps[(String, String)]).flatMap(f)
(consensusVariantReviewInfo: MonadOps[(String, String)]).map(f)
(consensusVariantReviewInfo: MonadOps[(String, String)]).withFilter(p)
Detailed information produced by
ReviewConsensusVariants
on variants called in consensus reads. Each row contains information about a consensus _read_ that carried a variant or non-reference allele at a particular variant site.The first 10 columns (up to
N
) contain information about the variant site and are repeated for each consensus read reported at that site. The remaining fields are specific to the consensus read.The chromosome on which the variant exists.
The position of the variant.
The reference allele at the position.
The genotype of the sample in question.
The set of filters applied to the variant in the VCF.
The count of A observations at the variant locus across all consensus reads.
The count of C observations at the variant locus across all consensus reads.
The count of G observations at the variant locus across all consensus reads.
The count of T observations at the variant locus across all consensus reads.
The count of N observations at the variant locus across all consensus reads.
The consensus read name for which the following fields contain values.
A description of the insert that generated the consensus read.
The base call from the consensus read.
The quality score from the consensus read.
The number of As in raw-reads contributing to the consensus base call at the variant site.
The number of Cs in raw-reads contributing to the consensus base call at the variant site.
The number of Gs in raw-reads contributing to the consensus base call at the variant site.
The number of Ts in raw-reads contributing to the consensus base call at the variant site.
The number of Ns in raw-reads contributing to the consensus base call at the variant site.