Sondovač is a script to create orthologous low-copy nuclear probes from transcriptome and genome skim data for target enrichment.
- Bug fixes, more robust coding.
- Updated documentation.
- Removed colorization of the output, simplified output for user, improved coding standard.
- Removed build-in software installation.
- Removed interactive mode, simplified code.
- bam2fastq is dropped in favour of samtools fastq. No plans to use Picard anymore (part A).
- Simplified INSTALL and README not to only copy PDF manual.
- Corrected output of part A - ensure to have always valid FASTA.
- Automatically remove putative plastid sequences from final probe set (part B), list of all probes (with putative plastid sequences) and list of putative plastid sequences are available.
- Updated software distributed with Sondovač, updated respective sections of PDF manual.
- Removed FASTX Toolkit, conversion from FASTQ to FASTA is done by simple shell function.
- Improved handling of input/output files when stored in several different directories.
- Tested with Geneious 10, improved description of Geneious usage in the PDF manual.
- Improved PDF manual.
- Fixed wrong probe design summary statistics (at the end of part B).
- Added support for Geneious 9.
- More detailed error reporting (especially in part B).
- Various smaller fixes.
- Updated accompanying software to recent versions.
- Checking if input FASTA files are interleaved or not (required) and, if needed, FASTA files are converted not to be interleaved.
- Added requirement of Python.
- Removed BAM files (part A) - they are not kept anymore.
- Language checking and enhancements of documentation.
- Modified CD-HIT-EST.
- Improved summary of the probe design in part B.
- More possibilities for minimum total locus length.
- Various smaller fixes.
- Renaming of input FASTA sequences names is required - it ensures correct working of part B.
- Added check if input files were created on Windows - if so, they are converted into UNIX style EOL.
- Various smaller fixes.
- Better showing of the information in part B.
- Enhanced documentation.
- Fixed error with some input files for part B.
- Finished colorization of command-line user interface.
- Added possibility to set minimal exon length of the loci.
- Various fixes and UI enhancements.
- Improved documentation.
- Offer the possibility to choose between transcripts or genome skim sequences for further processing.
- Colorization of command-line user interface (incomplete).
- Added possibility to change -minIdentity parameter of BLAT in step 11, part B.
- Fixed problems with some transcriptome input files.
- Added possibility to set custom bait length.
- Added information about article in MER introducing Sondovač.
- Highly enhanced part B.
- Better handling of variable output from Geneious.
- Possibility to specify custom output files name.
- Full support for Linux distributions using DEB - Debian, Ubuntu, Linux Mint and derivatives.
- Enhanced documentation.
- Support for Mac OS X, package management using Homebrew.
- Support for RedHat based Linux distributions - Fedora, Centos and Scientific Linux and derivatives.
- Better compilation and installation of required software.
- For downloading automatically select whether to use wget (preferred) or curl.
- Various fixes.
- Usage of mitochondrial reference sequence is optional.
- Better formatting of script messages.
- Various fixes and enhancements.
- Fixed reported problems with sed differences among Linux and Mac OS X.
- Added more exhaustive documentation.
- Various fixes and enhancements.
- Fixed problems with some versions of output of Geneious.
- Better compilation and installation of required additional software packages.
- Various fixes and enhancements.
- First public release, early alpha stage.