- Implemented method to check for overlap with genomic region for SVs and SNVs - Added ability to specify header, e.g., useful for reproducing VCF header
**Bugfixes**
- Fixed convert_files.py script to use new BaseFile methods
0.2.1
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**Bugfixes**
- Fixed (and renamed) method for getting file extension in BaseFile - Generalized support for compression file extensions
0.2.0
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**Features and Enhancements**
- Added Factera file type and parser - Added PavFinder VCF file type and parser - Refactored BaseFile to be more consistent and stable - Common instantiation method to ensure consistent attributes - add_obj now checks if obj is a CancerApiObject - Added buffersize option for files for autoflushing - Converted files automatically write out to disk
**Bugfixes**
- Fixed bugs relating to file conversion
0.1.5
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**Bugfixes**
- Fixed uninitialized attributes in BaseFile
0.1.4
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**Features and Enhancements**
- Moved garbage collection (for reduced memory usage) to `clear_storelist` method
**Bugfixes**
- The files submodule would incorrectly append to the same file between different runs. This has been fixed.