Ancestry / VCFcontam

Estimate NGS cross-sample contamination from VCF files with SVM

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VCFcontam

This module implements a method for estimating the continuous fraction of contamination of NGS sequencing reads by parsing relevant information from a VCF file.

Required packages:

pip3 install cython
pip3 install wheel
pip3 install pandas pysam numpy pomegranate scikit-learn

Input:

  • A VCF file that has been bgzipped with an accompanying tabix index file.

Output:

  • A float that represents the estimated contamination fraction.

Serialized model:

A serialized (pickled) model is used as input into predictSVR.py. This serialized model must have been generated using the exact save version of scikit-learn as that used in predictSVR.py.

Usage:

The model must first be trained and the model object serialized, after which a VCF can be used as input to generate a contamination prediction.

The training data can be generated as a separate step using a collection of VCFs with known contamination fractions using the following command:

python3 VCFcontam/generate_training_data.py --inputlist <vcflistfile> --loci <bed_file_for_feature_extraction> --feature_out <output_file_name>

where the file given to --inputlist is an unheadered two-column file where the first column is the (full) path to a (bgzipped and tabix-indexed) VCF file with a known contamination level, and the second column is a float value representing the known contamination level present in that VCF file. After generating the training data, the model can be trained using the following command:

python3 VCFcontam/trainSVR.py --training_data <feature_out_from_generate_training_data> --out <serialized_model_output_name>

Alternatively, the training data feature extraction and model fitting can all be performend in a single step by supplying trainSVR.py with a --vcf_metadata flag, supplying the same two-column tab-delimited file with the paths to the VCFs and the known contamination level of the VCFs, like so:

python3 VCFcontam/trainSVR.py --vcf_metadata <vcflistfile> --extracted_features <outputfilefortestfeatures> --out <serialized_model_output_name> --loci <bed_file_for_feature_extraction>

In the above command, the extracted features are written to an outfile specified by --extracted_features, the serialized model output is written to a file specified by --out.

To estimate contamination from a VCF after training the model, use the following command:

python3 VCFcontam/predictSVR.py --model <trained_model_object_file> --vcf <vcf_file> --index <vcf_file_tbi_index> --loci <bed_file_for_feature_extraction>

Citation:

McCartney-Melstad E, Bi K, Han J, Foo CK. 2021. VCFcontam: A Machine Learning Approach to Estimate Cross-Sample Contamination from Variant Call Data. bioRxiv doi:10.1101/2021.03.12.435007

https://www.biorxiv.org/content/10.1101/2021.03.12.435007v1

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Estimate NGS cross-sample contamination from VCF files with SVM

License:MIT License


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