0.11.0
- Documentation updates
- New script: @RPINerd added fasta/fasta_size_report.py
- New script: fastq/validate_mate_pairing.py
- New script: general/report_matrix_shape.py
- New script: gff/remove_fasta_from_gff3.py
- New script: gtf/convert_stringtie_gtf_to_gff3.py
- fasta/fasta_simple_stats.py: Critical fix - Script was missing stats on last/only sequence.
- general/filter_columnar_file.pl renamed to general/filter_columnar_file_by_column_values.pl
- lib/biocode/utils.py: Added function fasta_file_from_dict()
- lib/biocode/gff.py: gff.print_gff3_from_assemblies() no longer automatically splits genes with multiple mRNAs
- lib/biocode/gff.py: Fixed error causing failure if print_gff3_from_assemblies() was called
- fastq/randomly_subsample_fastq.py: Corrected shebang line which was causing failures
- fastq/fastq_simple_stats.py: Added (optional) progress interval reporting
- fastq/fastq_simple_stats.py: Added commas to integer outputs for better human readability
- blast/calculate_query_coverage_by_blast.py: Added error handling so it reports/dies gracefully if an input seq isn't found
- fasta/filter_fasta_by_ids.pl: minor: added additional info if in debugging mode
- general/join_columnar_files.py: Corrected issue where header line was printing to STDOUT rather than output file
- gff/convert_tRNAScanSE_to_gff3.pl: @pgonzale60 committed improvements to satisfy NCBI's table2asn_GFF requirements
- fastq/fastq_simple_stats.py: Fixed issues where script would fail if file had no entries
- Critical bugfix and general improvements to sandbox/export_pasa_unigenes.py
Contributors
RPINerd and pgonzale60