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<div id="termynal" data-termynal>
<span data-ty="input">bitia run "samtools convert < foo.fa|http://y.com/foo.fa >"</span>
<span data-ty="progress"></span>
</div>
- Checks for the input file `foo.fa` in the current working directory
- Download the input file from the given link `http://example.com/foo.fa` and name it `foo.fa`
- Add the given command `samtools convert <foo.fa|http://example.com/foo.fa` into a pipeline file.
- Extract the current working directory with the pipeline as a zip file that contains a unique hash and send it to the server `public.bitia.link`
- The BiTIA runner in the server will execute the pipeline by:
- Installing the given command `samtools`
- Downloading the given input file from the link `http://example.com/foo.fa` and name it `foo.fa`
- Executing the command `samtools convert foo.fa`
<div id="termynal" data-termynal>
<span data-ty="input">bitia run "samtools convert < foo.fa|http://y.com/foo.fa >"</span>
<span data-ty="progress"></span>
</div>
for `pipeline.sh`:
```bash
#!/usr/bin/env bash
fastqc *.gz
for file in *_1.fastq.gz
do
trim_galore --cores 8 --gzip --fastqc --max_n 2 --output_dir Trimmed_Data/ --paired $file ${file%_1.fastq.gz}_2.fastq.gz
done
hisat2-build -p 8 ./Homo_sapiens/UCSC/hg38/Sequence/WholeGenomeFasta/genome.fa index
```
- Extract the current working directory with the `pipeline.sh` as a zip file containing a unique hash and send it to the public `server.bitia.link`
- The BiTIA runner in the server will execute the pipeline .
- Installing the given commands `fastqc`, `trim_galore`,`hisat2`.