1. Add a rule that generates [FastQC](https://www.bioinformatics.babraham.ac.uk/projects/fastqc/) reports for the two input fastq.gz files.
* The tool `fastqc` is available from the `bioconda` conda channel.
* An example command-line to use `fastqc` is
```
$ fastqc chip-seq/H3K4-TC1-ST2-D0.12.fastq.gz
```
* The output are two files in the same directory as the input file, `H3K4-TC1-ST2-D0.12_fastqc.html` and `H3K4-TC1-ST2-D0.12_fastqc.zip`.
* You might want to copy at least the html file to the `output` directory.
* Do not forget to add at least one of the output files to the summary rule or explicitly specify it on the command-line.
2. Add a rule that generates alignment statistics for the two bam files with [Picard](https://broadinstitute.github.io/picard/)[CollectAlignmentSummaryMetrics](https://broadinstitute.github.io/picard/command-line-overview.html#CollectAlignmentSummaryMetrics).
* The tool `picard` is available from the `bioconda` conda channel.