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Latest version: v4.0.81

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4.0.51

Added `--reverse` and `--complement` options to `bin/fasta-find.py` to tell
it to also look for simple inversions and complement sequences.

4.0.50

Added `bin/fasta-find.py` which, like `bin/fasta-match-offsets.py`, also
reports matching sequence offsets in FASTA files but can match numeric
regions and also look for reverse complemented matches.

4.0.49

Added `bin/fasta-match-offsets.py` to print offsets of sequence regular
expression matches.

4.0.48

More careful calling of `pysam.pileup` in `sam-coverage-depth.py` to avoid
an index error if a read mapping extends beyond the end of the reference
genome. `pysam` was returning an invalid `column.reference_pos` in that
case (invalid because the value is beyond the end of the reference, so it
can't be used as a reference offset).

4.0.47

Added printing of transversion and transition counts to
`bin/codon-distance.py`. Output is sorted first by distance, then by number
of transitions (highest to lowest) then by codon DNA. The idea being to
present the possible codon changes to get from one amino acid to another in
the order that requires the least change to the most.

The lists in the values in the dict returned by `codonInformation` now
contain 2-tuples instead of lists of length 2. If you pass
`countTransitions=True` to that function it will also put the count of the
number of transitions (as opposed to transversions) into the tuple. See the
tests in `test/test_codonDistance.py`.

4.0.46

Added `--reference` option to `sam-coverage-depth.py`.

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