Prepare version 1.1

[northwestwitch]

[1.1]

Added

• Support for tab-delimited (\t) files in csv_2_json endpoint

  Fixed

• Do not crash when parsing Variant CSV files with no assertion criteria

This version is a:

• [ ] MAJOR - when you make incompatible API changes
• [x] MINOR - when you add functionality in a backwards compatible manner
• [ ] PATCH - when you make backwards compatible bug fixes or documentation/instructions

[codecov-commenter]

Codecov Report

Base: 98.03% // Head: 98.03% // No change to project coverage :thumbsup:

Coverage data is based on head (2c47437) compared to base (4d66d42). Patch coverage: 100.00% of modified lines in pull request are covered.

Additional details and impacted files

```diff @@ Coverage Diff @@ ## main #50 +/- ## ======================================= Coverage 98.03% 98.03% ======================================= Files 9 9 Lines 254 254 ======================================= Hits 249 249 Misses 5 5 ``` | Flag | Coverage Δ | | |---|---|---| | unittests | `98.03% <100.00%> (ø)` | | 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/50?src=pr&el=tree&utm_medium=referral&utm_source=github&utm_content=comment&utm_campaign=pr+comments&utm_term=Clinical-Genomics) | Coverage Δ | | |---|---|---| | [preClinVar/\_\_version\_\_.py](https://codecov.io/gh/Clinical-Genomics/preClinVar/pull/50/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)` | | 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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[northwestwitch]

I'm going to close this and create a major version 2.0, since I'll be introducing breaking changes to keep up with changes in the ClinVar API introduced on 2022-11-21