@@ -18,7 +18,7 @@ families and the number of ancient sequences found.
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Execute quicksand like this::
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- nextflow run mpieva/quicksand -r v2.1 \
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+ nextflow run mpieva/quicksand -r v2.2 \
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-profile singularity \
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--split split/ \
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--db refseq/kraken/Mito_db_kmer22/ \
@@ -29,7 +29,7 @@ The output files are grouped by family-level in the :code:`out/` directory. Extr
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after the KrakenUniq run are stored in :code: `out/{family}/1-extracted/ ` while mapped, deduped and filtered sequences are saved to the
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:code: `out/{family}/best/{step}/ ` directory after the respective processing step::
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- quicksand_v2.1
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+ quicksand_v2.2
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├── out
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│ └── {family}
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│ ├── 1-extracted
@@ -65,7 +65,7 @@ file-names and should be unique!::
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and start the execution with::
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- nextflow run mpieva/quicksand -r v2.1 \
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+ nextflow run mpieva/quicksand -r v2.2 \
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-profile singularity \
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--split split/ \
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--db refseq/kraken/Mito_db_kmer22/ \
@@ -77,7 +77,7 @@ The output file structure remains the same as before. For families specified in
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appear in the :code: `out/{family}/fixed/{step}/ ` directory, together with additional output-files
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that are useful in additional downstream-analyses, such as the extracted deaminated reads::
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- quicksand_v2.1
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+ quicksand_v2.2
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├── out
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│ └── {family}
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│ ├── 1-extracted
@@ -122,14 +122,14 @@ After collecting the reference genome(s) for the Suidae family, prepare a fresh
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and rerun the pipeline with::
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- nextflow run mpieva/quicksand -r v2.1 \
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+ nextflow run mpieva/quicksand -r v2.2 \
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-profile singularity \
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--rerun \
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--fixed fixed-references.tsv
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The (additional) output files are the ones created by the :code: `--fixed ` flag::
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- quicksand_v2.1
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+ quicksand_v2.2
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├── out
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│ └── {family}
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│ ├── 1-extracted
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