Workflow Type: Galaxy
Open
Galaxy workflow
Inputs
ID | Name | Description | Type |
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Collection of VCFs to analyze | #main/Collection of VCFs to analyze | n/a |
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Reference genome of the MTBC ancestor | #main/Reference genome of the MTBC ancestor | n/a |
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Steps
ID | Name | Description |
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2 | Filter TB variants | We will ensure at this step that variants to build the MSA are fixed variants and that we low-confidence filter repetitive regions of the MTB genome toolshed.g2.bx.psu.edu/repos/iuc/tb_variant_filter/tb_variant_filter/0.1.3+galaxy0 |
3 | Generate the complete genome of each of the samples | The complete genome of each of the samples is generated by inserting the SNPs defined in the respective VCF in the reference genome that was used for mapping and SNP calling toolshed.g2.bx.psu.edu/repos/iuc/bcftools_consensus/bcftools_consensus/1.9+galaxy2 |
4 | Concatenate genomes to build a MSA | All genomes are concatenated in a single multifasta file. Because all o them have the same length, this may be seen as a multiple sequence alignment. toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_cat/0.1.1 |
5 | Keep only variable positions | Discard invariant positions from the MSA to simplify the file so only contains positions with at least one SNP in at least one strain. toolshed.g2.bx.psu.edu/repos/iuc/snp_sites/snp_sites/2.5.1+galaxy0 |
6 | Calculate SNP distances | From the MSA. Calculate pairwise SNP distances between samples. toolshed.g2.bx.psu.edu/repos/iuc/snp_dists/snp_dists/0.6.3+galaxy0 |
Outputs
ID | Name | Description | Type |
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{input_file} | #main/{input_file} | n/a |
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_anonymous_output_1 | #main/_anonymous_output_1 | n/a |
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_anonymous_output_2 | #main/_anonymous_output_2 | n/a |
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_anonymous_output_3 | #main/_anonymous_output_3 | n/a |
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_anonymous_output_4 | #main/_anonymous_output_4 | n/a |
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Version History
2 (earliest) Created 22nd Apr 2024 at 11:19 by Helena Rasche
Added/updated 3 files
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Created: 22nd Apr 2024 at 11:19
Last updated: 22nd Apr 2024 at 11:19
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