Skip to content

Version 2 of the PROSIC caller for somatic variants.

License

Notifications You must be signed in to change notification settings

varlociraptor/prosic2

Folders and files

NameName
Last commit message
Last commit date

Latest commit

 

History

85 Commits
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Repository files navigation

Postprocessing for Somatic Mutation Calling (PROSIC)

install with bioconda Anaconda-Server Badge

Prosic has been succeeded by Varlociraptor. Please use Varlociraptor instead.

PROSIC is a caller for somatic variants in tumor-normal sample pairs, sequenced with any next-generation sequencing technology. It provides a novel latent variable model that integrates various levels of uncertainty, and thereby allows to properly asses the probability of having a somatic variant while controlling the false discovery rate.

Installation

PROSIC is available via Bioconda, a distribution of bioinformatics software for the conda package manager. Bioconda can be set up in any Linux environment, even without admin rights. With Bioconda set up, PROSIC can be installed via

$ conda install prosic

Usage

The purpose of PROSIC is to call somatic insertions and deletions (indels) on tumor/normal sample pairs. For this, PROSIC requires a VCF file with preliminary indel calls, e.g. obtained with Delly or Lancet. Then, calling with PROSIC consists of two steps.

Step 1: Calling

Variants are called by applying PROSIC to the preliminary calls, i.e.

$ prosic call-tumor-normal --flat-priors tumor.bam normal.bam < pre-calls.vcf > prosic-calls.bcf

PROSIC then annotates the initial calls with probabilities for the events somatic, germline and absent (PROB_SOMATIC, PROB_GERMLINE, PROB_ABSENT). Issue prosic tumor-normal --help for information about additional parameters.

Step 2: Controlling FDR

To control the FDR, you first have to create a null-model by swapping tumor and normal bams. In case of a general purpose caller like Delly, you can use the same vcf of preliminary calls. With callers like lancet, you have to create a vcf with swapped samples. Then, you apply prosic call-tumor-normal (Step 1) with swapped tumor and normal bams, i.e.

$ prosic call-tumor-normal --flat-priors normal.bam tumor.bam < null-pre-calls.vcf > null-calls.bcf

Finally the FDR (here for somatic deletions) can be controlled by

$ prosic control-fdr --event SOMATIC --var DEL < null-calls.bcf > thresholds.tsv

The resulting tab-separated table thresholds.tsv contains thresholds that can be applied to the corresponding PROB_SOMATIC field in prosic-calls.bcf, in order to control the FDR at different levels.

Authors