Contents of this Version_2.6 directory: ======================================= If you wish to do assembly or mapping using the Newbler software, then download items (1), (2) and (3) from the list below: (1) DataAnalysis_2.6_All.tgz = Newbler assembler, mapper, Amplicon variant analyser, and sffinfo/sfffile software. Runs on Linux ONLY. (2) Manual-v2.6_Overview_May2011.pdf = Overview of roche software, including sffinfo, sfffile (3) Manual-v2.6_PartC_Assembly_and_Mapping_May2011.pdf = PDF file of Manual for Newbler Assembly and Mapping programs. (4) Manual-v2.6_PartD_AmpliconVariantAnalyzer_May2011.pdf = PDF file of manual for the Amplican Variant Analyser. (5) Documentation_2.6_All_as_many_html_pages.tgz = Documentation as many HTML files. This software should install without problem on Fedora, Redhat and CentOS versions of Linux. However, on Ubuntu you may receive an error message during installation. A work-around is: (a) On Ubuntu, the "Nixstaller" installer used in the installation package will probably stop with the following error: Cannot execute command: type rocks2>&1 A work-around is to create a link so rocks always returns true: ln -s /bin/true ~/bin/rocks ( for more info see: http://seqanswers.com/forums/showthread.php?t=8944 post number '#9' ) (b) For the Newbler assembler itself there are both 64 bit and 32-bit versions in the one package, but the GUI part of the Roche software seems to be only 32-bit, so the installation may complain about: "libraries not found : zlib.i386, libXi.i386, libXtst.i386, libXaw.i386" On Ubuntu, to install these 32-bit libraries, you can use: sudo apt-get install ia32-libs To run the Newbler assembler from the command-line, typically use: (a) For Genome data: runAssembly -urt -het -o assembly1 reads.sff where: "-urt" means "use read tips" to extend contigs across low coverage regions, "-het" is for reads from heterogenous sample -eg. from several individuals or diploid. (b) For Transcriptome data: runAssembly -urt -cdna -vt AdaptersToTrimFromReads.fna -o assembly1 reads.sff where: "-cdna" indicates reads are cDNA, so consider alternative splicing, and large reange of coverage. "-vt .." to trim adapters, such as MINT or SMART adapters used to synthesis the cDNA, from the reasd before assembly. Several additional options can be use, such as "-vs ScreeningFile.fna" can optionally be used. See manual for more details.