Table — NodePit

There are 2898 nodes that can be used as successor for a node with an output port of type

STAR aligns RNA-seq reads to a reference genome using uncompressed suffix arrays and is "splice aware".

Filters and prioritizes genetic variants from whole exome sequencing data.

SnpEff annotates and predicts the effects of genetic variants.

This node is a wrapper for the SnpSift toolbox.

Variant Effect Predictor (VEP) - annotates genomic variants.

This node filters VCF files annotated by VEP.

Combines any number of gVCF files that were produced by the Haplotype Caller into a single joint gVCF file.

Combines any number of VCF lists that were produced by Pindel into a single joint VCF file.

Assess sequence coverage by a wide array of metrics, partitioned by sample, read group, or library.

Recalibration of sequencing quality scores.

Node Connectivity