@@ -18,7 +18,7 @@ families and the number of ancient sequences found.
1818
1919Execute quicksand like this::
2020
21- nextflow run mpieva/quicksand -r v2.1 \
21+ nextflow run mpieva/quicksand -r v2.2 \
2222 -profile singularity \
2323 --split split/ \
2424 --db refseq/kraken/Mito_db_kmer22/ \
@@ -29,7 +29,7 @@ The output files are grouped by family-level in the :code:`out/` directory. Extr
2929after the KrakenUniq run are stored in :code: `out/{family}/1-extracted/ ` while mapped, deduped and filtered sequences are saved to the
3030:code: `out/{family}/best/{step}/ ` directory after the respective processing step::
3131
32- quicksand_v2.1
32+ quicksand_v2.2
3333 ├── out
3434 │ └── {family}
3535 │ ├── 1-extracted
@@ -65,7 +65,7 @@ file-names and should be unique!::
6565
6666and start the execution with::
6767
68- nextflow run mpieva/quicksand -r v2.1 \
68+ nextflow run mpieva/quicksand -r v2.2 \
6969 -profile singularity \
7070 --split split/ \
7171 --db refseq/kraken/Mito_db_kmer22/ \
@@ -77,7 +77,7 @@ The output file structure remains the same as before. For families specified in
7777appear in the :code: `out/{family}/fixed/{step}/ ` directory, together with additional output-files
7878that are useful in additional downstream-analyses, such as the extracted deaminated reads::
7979
80- quicksand_v2.1
80+ quicksand_v2.2
8181 ├── out
8282 │ └── {family}
8383 │ ├── 1-extracted
@@ -122,14 +122,14 @@ After collecting the reference genome(s) for the Suidae family, prepare a fresh
122122
123123and rerun the pipeline with::
124124
125- nextflow run mpieva/quicksand -r v2.1 \
125+ nextflow run mpieva/quicksand -r v2.2 \
126126 -profile singularity \
127127 --rerun \
128128 --fixed fixed-references.tsv
129129
130130The (additional) output files are the ones created by the :code: `--fixed ` flag::
131131
132- quicksand_v2.1
132+ quicksand_v2.2
133133 ├── out
134134 │ └── {family}
135135 │ ├── 1-extracted
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