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Mutational antigenic profiling of ZIKV E protein

Experiments by Caroline Kikawa, Jackson Barr Stuart and Leslie Goo. Analysis by Jesse Bloom and Caroline Kikawa.

Results

For a summary of the results, see selections_analysis.ipynb.

Other results are placed in ./results/, although not all files are tracked in the GitHub repo.

  • Barcoded subamplicon sequencing reads are processed into codon counts, and stored in ./results/codoncounts/
  • For individual and median antibody escape values, see differential selection measurements, placed in ./results/diffsel/.
  • PDB files with reassigned B-factors with antibody escape are placed in ./results/reassignedpdb/.

For the data and analysis used in the neutralization assays and visualizations for the paper, see the notebooks and results in ./paper_figures/, and for documentation of the SRA sequencing submission, see ./sra_submission/

Running analysis

First activate the conda environment for the analysis. If you have prebuilt the relevant environments, you can do this just with:

conda activate zikv_dmstools2

or:

conda activate neutcurve

Otherwise, first build the conda environments from the environments/environment_dmstools2.yml or environments/environment_neutcurve.ymlfile, then activate it as above.

After you have activated the either conda environment, simply run the Python Jupyter notebooks: use environment_dmstools2 to run selections_analysis.ipynb or polyclonal_analysis.ipynb. On the Hutch cluster, you will first want to grab a node with 16 cores before doing this. For the notebooks within ./paper_figures/, use environment_neutcurve.

Input data

The input data are in ./data/:

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