@@ -68,7 +68,7 @@ Bactopia on. We will look at the following inputs:
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### Illumina and/or Nanopore Reads
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- Let's start with the most common inputs, plain old FASTQ files for a _ single sample_ . Bactopia
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+ Let's start with the most common inputs, plain on FASTQ files for a _ single sample_ . Bactopia
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accepts both Illumina (pair-end or single-end) and Nanopore reads, and can even process them
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together for a hybrid assembly.
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@@ -218,7 +218,7 @@ file will be processed by Bactopia just like your normal local FASTQs.
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!!! question "Why only Experiment accessions?"
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In the grand scheme of accession hierarchies, Experiment accessions are really the only
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unique ones. For example, a multiple Run accessions can be associated with a single
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- Experiment accession. Or, multiple Experiment accessions can be associated with a single
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+ Experiment accession. Or, multiple Exeriment accessions can be associated with a single
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BioSample accession. So, by using Experiment accessions, you can be confident you are
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getting only the sequences associated with that "_ unique_ " Experiment.
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@@ -247,7 +247,7 @@ to go fetch the associated assembly and process it just like a local assembly.
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```
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!!! question "Do I need to provide the assembly version? (e.g. GCF_000000000.1)"
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- Over time I've found the assembly version to be unstable. For example, sometimes
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+ Overtime I've found the assembly version to be unstable. For example, sometimes
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an assembly might be corrected, and the previous version is not made available
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any longer. So, to avoid any issues, Bactopia will always use the latest version
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of a given NCBI Assembly accession.
@@ -623,7 +623,7 @@ With this, Nextflow will use Docker to run all the processes in Bactopia (even t
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Bactopia is installed with Conda!).
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!!! tip "Always prefer containers over Conda"
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- While I will be the first to admit that I love Conda, it is not perfect. Over time tools
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+ While I will be the first to admit that I love Conda, it is not perfect. Overtime tools
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can become broken or incompatible due to dependencies. Containers are a great way
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to avoid these issues. If you are using Bactopia, and have Docker or Singularity
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available I would recommend using them over Conda.
@@ -742,4 +742,4 @@ successfully, the appropriate results are pulled out and placed in the sample's
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The ` work ` directory can grow very large very quickly! Please keep this in mind when using
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Bactopia (_ and other Nextflow pipelines_ ). To help prevent the build up of the ` work `
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directory you can use ` --cleanup_workdir ` to automatically delete the ` work ` directory after
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- a successful run.
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+ a successful run.
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