VCF parser using the Python pandas library for interactive analysis
VCF header parsing requires the tabix -H command which is broken in tabix version 1.2.X Please update your tabix version to 1.3.pandasVCF handles both multi-sample and single-sample VCF files. Please see ipynb/ for usage. pandasVCFmulti and pandasVCFsingle are now depracated.
pandasVCFmulti now handles both multi-sample and single-sample VCF files. Please see http://nbviewer.ipython.org/github/erscott/pandasVCF/blob/master/ipynb/multi_sample_ex.ipynb for usage. pdVCFsingle.py is now depracated and will be removed in the near future.
Command line support will be added in the near future.
pdVCFsingle.py can now parse a dataframe with a single individual, either from a multi-sample VCF or a single-sample VCF. Missing genotype calls maked with '.' are dropped when add_variant_annotations are called. 100,000 variants are parsed in ~10sec.