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Copy file name to clipboardexpand all lines: README.md
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```
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```bash
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.
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├── .vscode
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│ ├── configurationCache.log
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│ ├── dryrun.log
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│ ├── settings.json
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│ └── targets.log
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├── VF
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│ ├── examples
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│ │ └── README.md
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│ ├── README.md
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│ └── dependencies.sh
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├── .DS_Store
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├── README.md
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└── tree.txt
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└── README.md
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```
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```
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## Framework Overview
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## Variant Filtering (VF)
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VF is a prototype software implementation of our algorithms for variant filtering in variation graphs for the problems 1 to 4.
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## VF_Experiments
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VF_Experiments is a framework to establish a benchmark for datasets and tools needed to evaluate the VF experiments and the impact of read-to-graph mappers.
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## Havg (Haplotype-annotated Variation Graph)
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Havg is used to create a variation graph that corresponds to each chromosome, annotated with a list of haplotypes per edge when the graph only contains SNP variants. This annotated graph is then used in solving problems 5 and 6.
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## hg (Haplotype-aware Graphs)
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This repository constructs an ILP solution for haplotype-aware variant selection for genome graphs under Hamming distance for solving problems 5 and 6.
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## hged (Haplotype-aware Edit Distance)
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This repository constructs an ILP solution for haplotype-aware variant selection for genome graphs under Hamming distance for solving problems 7 and 8.
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