Artemis is designed to help you view DNA sequences and insert annotations. It allows visualisation of sequence features and the results of analyses within the context of the sequence, and its six-frame translation.

Artemis is a genome browser and annotation tool that allows visualisation of sequence features, next generation data and the results of analyses within the context of the sequence, and also its six-frame translation.

Artemis is written in Java, reads EMBL or GENBANK format sequences and feature tables, and can work on sequences of any size.

What's New in This Release: [ read full changelog ]

· Added option to provide overview of the variation sites
· Change BamView filter to enable filtering in and out based on reads flag
· Add read count and RPKM calculations to BamView
· Add option in BamView to clone the alignment panel
· Create features option for VCF records
· Unit tests added for writing VCF/BCF sequences
· Add new Coverage view to BamView. It automatically switches to this view on zooming out
· Add options to write out or view FASTA sequences from VCF/BVF variation data