vcfpy 0.3.0

Why another VCF parser for Python!

I’ve been using PyVCF with quite some success in the past. However, the main bottleneck of PyVCF is when you want to modify the per-sample genotype information. There are some issues in the tracker of PyVCF but none of them can really be considered solved. I tried several hours to solve these problems within PyVCF but this never got far or towards a complete rewrite…

For this reason, VCFPy was born and here it is!

What’s the State?

VCFPy is the result of two full days of development plus some maintenance work later now (right now). I’m using it in several projects but it is not as battle-tested as PyVCF.

Why Python 3 Only?

As I’m only using Python 3 code, I see no advantage in carrying around support for legacy Python 2 and maintaining it. At a later point when VCFPy is known to be stable, Python 2 support might be added if someone contributes a pull request.

HEAD

• Reader and Writer can now be used as context manager (with with)

• Including license in documentation, including Biopython license

• Adding support for writing bgzf files (taken from Biopython)

• Adding support for parsing arrays in header lines

• Removing example-4.1-bnd.vcf example file because v4.1 tumor derival lacks ID field

• Adding AltAlleleHeaderLine, MetaHeaderLine, PedigreeHeaderLine, and SampleHeaderLine

• Renaming SimpleHeaderFile to SimpleHeaderLine

• Warn on missing FILTER entries on parsing

• Reordered parameters in from_stream and from_file (#18)

• Renamed from_file to from_stream (#18)

• Renamed Reader.jump_to to Reader.fetch

• Adding header_without_lines function

• Generally extending API to make it esier to use

• Upgrading dependencies, enabling pyup-bot

• Greatly extending documentation

0.2.1 (2016-09-19)

• First release on PyPI