There are 3946 nodes that can be used as predessesor
for a node with an input port of type Table.
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features.
This node can be used to merge statistics of the featureCounts node.
Tools to manipulate SAM/BAM files
Pindel - a pattern growth approach to detect breakpoints of large deletions and medium sized insertions from paired-end reads.
This node sorts the chromosomes of an input VCF file analogous to a given reference sequence.
This node filters annotated VCF files.
FastQC - Quality check for NGS read data.
FastQC - A quality control tool for high throughput sequence data.
This node can be used to merge statistics of FastQC modules.
The RawReadManipulator filters reads from fastQ/fastA files.