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Releases: treangenlab/Olivar

v1.2.1

01 Oct 01:01
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  • FASTA header ID is used as the reference name by default, instead of the name of the FASTA file.
    The header ID is everything before a space character in the FASTA header ("EPI_ISL_402124" for EPI_ISL_402124.fasta). This will change the names and content of several output files, including

    1. Default name of the .olvr file
    2. Output file names of olivar tiling (e.g., EPI_ISL_402124.html)
    3. Columns in olivar-design.csv and olivar-design.primer.bed, as well as outputs of olivar validate (e.g., olivar-val_pool-1.csv)
  • Fixed BED/ARTIC output format (see issue #17)

v1.2.0

16 Sep 01:44
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  • Support for multiple tiling targets (e.g., designing tiled amplicons for each Influenza A segment)
    • olivar tiling can also take multiple .olvr files in the same directory as input, and amplicons under each target will now have their names determined by the file name of the corresponding .olvr file (e.g., olivar-ref.olvr)
    • design title (olivar tiling --title) will not affect amplicon names, and will only determine output files names for the whole design (e.g., olivar-design.csv and olivar-design.scheme.bed)
    • output files are also generated for each target, including the html plot showing primers and risk scores (see the updated example_output/)
  • Fixed incorrect coordinates in .scheme.bed files (issue #14)

v1.1.5

19 Jun 06:25
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  • Change license to GPL v3.0

v1.1.4

04 Feb 06:48
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  • Updated Loss function for short genomes (Loss is multiplied by 1/coverage^2).
  • Added error messages for ambiguous bases (non 'A', 'T', 'C', 'G' bases).
  • Fixed compatibility issues with Biopython (Bio.Blast.Applications.NcbiblastnCommandline have been deprecated).

v1.1.3

09 Oct 06:25
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  • Improved backward compatibility

v1.1.2

17 Sep 03:37
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  • Sanity check for input reference genome and variant list, with error messages for ambiguous bases and invalid values.
  • Additional output file in ARTIC/PrimalScheme format.
  • Bug fixed: when multiple variants with the same genome position is provided, the sum of frequencies of each variant should be calculated first, then the square root.
  • Amplicon name is now the same as user provided title.