ivar - functions broadly useful for viral amplicon-based sequencing
Contents
Commans
trim Trim reads in aligned BAM file
variants
Call variants from aligned BAM file
filtervariants
Filter variants across replicates or samples
consensus
Call consensus from aligned BAM file
getmasked
Detect primer mismatches and get primer indices for the amplicon to be masked
removereads
Remove reads from trimmed BAM file
version
Show version information
To view detailed usage for each command type `ivar <command>`
Description
iVar is a computational package that contains functions broadly useful for viral amplicon-based
sequencing. Additional tools for metagenomic sequencing are actively being incorporated into iVar. While
each of these functions can be accomplished using existing tools, iVar contains an intersection of
functionality from multiple tools that are required to call iSNVs and consensus sequences from viral
sequencing data across multiple replicates.
Name
ivar - functions broadly useful for viral amplicon-based sequencing
Synopsis
ivar [command<trim|variants|filtervariants|consensus|getmasked|removereads|version|help>]
