Skip to content

Releases: bcgsc/pori_graphkb_python

Release v1.15.0

04 Dec 22:55
f3a17ae
Compare
Choose a tag to compare

Release v1.15.0

New Feature:

  • KBDEV-1136 change cancergene and cancerrelated field-names to cancerGeneListMatch and kbStatementRelated

What's Changed

Full Changelog: v1.14.0...v1.15.0

Release v1.14.0

21 Nov 20:07
37f6528
Compare
Choose a tag to compare

Feature:

  • Add cancerGene flag to get_gene_information()

Release v1.13.0

03 Nov 21:13
6114071
Compare
Choose a tag to compare

Feature:

  • Add get_cancer_genes()

Release v1.12.0

11 Sep 18:33
665b82a
Compare
Choose a tag to compare

Feature:

  • Add type screening and length threshold for structural variant matching
  • Add dataset file reference for tests

Bugfix:

  • Fix relevance filtering for cancer predisposition function

v1.11.0

14 Jun 23:01
59d6ca2
Compare
Choose a tag to compare

Release v1.11.0

New Feature:

  • GERO-337 - get_gene_information function added.
    Improvements:
  • update docstrings and import orders

Release v1.10.2

24 May 17:47
d79c449
Compare
Choose a tag to compare

Bugfix:

  • match.py::match_positional_variant() using equivalent terms in lieu of whole tree for list of matching types

Release v1.10.1

09 May 23:03
727c329
Compare
Choose a tag to compare

Bugfix:

  • Update GH workflow for PyPi publishing on released

Release v1.10.0

08 May 22:29
18a0140
Compare
Choose a tag to compare

New feature:

  • New utility functions to accomodate for positional variant comparison

Bugfix:

  • fix match.py::match_positional_variant() not to use matched generic variants in 'similarTo' queries
  • require install of requests<2.29.0 to avoid any errors with urllib

Release v1.9.1

20 Mar 21:47
60445de
Compare
Choose a tag to compare

Improvements

  • Add support for GeneralizationOf edges in matching positional variants

Bugfix

  • Fix mkdocs redirect mapping for matching directory

Release v1.9.0

22 Feb 22:38
09b33b2
Compare
Choose a tag to compare

What's Changed

New Contributors

Full Changelog: v1.8.0...v1.9.0

Release v1.9.0
New Features:

  • get_statements_from_variants - helper function added.
  • get_term_list - helper function added.
  • get_rid - helper function added.
  • get_pharmacogenomic_info - helper function added.
  • get_cancer_predisposition_info - helper function added.
  • Added constants PHARMACOGENOMIC_RELEVANCE_TERMS and PHARMACOGENOMIC_SOURCE_EXCLUDE_LIST
    Bugfix:
  • Ignore gene name version in get_equivalent_features. Eg. NM_033360.4 should match 'NM_033360' and 'KRAS'.
    Improvements:
  • get_preferred_gene_name - moved to genes.py
  • move CHOMOSOMES and PREFERRED_GENE_SOURCE to constants.py
  • add retries on connection failure
    added tests:
  • test_get_pharmacogenomic_info
  • test_get_cancer_predisposition_info
  • reduced runtime of longest test
  • add match test