There are 2898 nodes that can be used as successor for a node with an output port of type Table.
Calls germline SNPs and indels via local re-assembly of haplotypes.
Computes the most likely genotype combination and phases trios and parent/child pairs.
Realignment around insertions and deletions.
Selects a subset of variants from a larger callset.
Calls SNPs and indels.
Filters variant calls based on INFO and FORMAT annotations.
Performs joint genotyping on gVCF files produced by HaplotypeCaller.
This node merges two VCF files into one combined VCF file.
Creates a Gaussian mixture model by looking at the annotations values over a high quality subset of the input call set and then evaluate all input variants.
This node uses the DESeq package to test for differential expression based on a model using the negative binomial distribution.
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