Clinical-Genomics / preClinVar

A ClinVar API submission helper written in FastAPI
MIT License
1 stars 0 forks source link

Prepare new patch 1.0.2 #45

Closed northwestwitch closed 1 year ago

northwestwitch commented 1 year ago

[1.0.2]

Fixed

This version is a:

codecov-commenter commented 1 year ago

Codecov Report

Base: 93.86% // Head: 97.85% // Increases project coverage by +3.98% :tada:

Coverage data is based on head (e5c523e) compared to base (db25514). Patch coverage: 98.86% of modified lines in pull request are covered.

Additional details and impacted files ```diff @@ Coverage Diff @@ ## main #45 +/- ## ========================================== + Coverage 93.86% 97.85% +3.98% ========================================== Files 7 9 +2 Lines 163 233 +70 ========================================== + Hits 153 228 +75 + Misses 10 5 -5 ``` | Flag | Coverage Δ | | |---|---|---| | unittests | `97.85% <98.86%> (+3.98%)` | :arrow_up: | Flags with carried forward coverage won't be shown. [Click here](https://docs.codecov.io/docs/carryforward-flags?utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#carryforward-flags-in-the-pull-request-comment) to find out more. | [Impacted Files](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics) | Coverage Δ | | |---|---|---| | [preClinVar/csv\_parser.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-cHJlQ2xpblZhci9jc3ZfcGFyc2VyLnB5) | `97.95% <93.33%> (ø)` | | | [preClinVar/\_\_version\_\_.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-cHJlQ2xpblZhci9fX3ZlcnNpb25fXy5weQ==) | `100.00% <100.00%> (ø)` | | | [preClinVar/build.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-cHJlQ2xpblZhci9idWlsZC5weQ==) | `100.00% <100.00%> (ø)` | | | [preClinVar/constants.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-cHJlQ2xpblZhci9jb25zdGFudHMucHk=) | `100.00% <100.00%> (+100.00%)` | :arrow_up: | | [preClinVar/demo/\_\_init\_\_.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-cHJlQ2xpblZhci9kZW1vL19faW5pdF9fLnB5) | `100.00% <100.00%> (ø)` | | | [preClinVar/main.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-cHJlQ2xpblZhci9tYWluLnB5) | `94.54% <100.00%> (+10.76%)` | :arrow_up: | | [tests/test\_main.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-dGVzdHMvdGVzdF9tYWluLnB5) | `100.00% <100.00%> (ø)` | | | [preClinVar/validate.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/45/diff?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics#diff-cHJlQ2xpblZhci92YWxpZGF0ZS5weQ==) | `100.00% <0.00%> (+7.69%)` | :arrow_up: | Help us with your feedback. Take ten seconds to tell us [how you rate us](https://about.codecov.io/nps?utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics). Have a feature suggestion? [Share it here.](https://app.codecov.io/gh/feedback/?utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics)

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