Description: Short read RNASeq de novo assembly is a well established method to study transcription of organisms lacking a reference genome sequence. Available software packages such as Trinity and Oases have proven to be able to build high quality contigs from short reads. But there is still room for improvement on different points such as i) compactness: they often produce different contigs which are included in one another or overlapping one another, ii) chimerism: the contigs contain different kinds on chimera such as duplicated open reading frames, iii) substitution, insertion, deletion errors: the consensus sequences build by the assembler contain errors which can be partly corrected using the read alignments.
Availability: DRAP code is freely available on the mulcyber forge.
Partners: team SIGENAE.
Availability: FROGS code is freely available on GitHub.