NAME
ataqv - QC metrics for ATAC-seq dataDESCRIPTION
ataqv 1.3.0: QC metrics for ATAC-seq data Usage: ataqv [options] organism alignment-filewhere:
- organism is the subject of the experiment, which determines the list of autosomes (see "Reference Genome Configuration" below).
- alignment-file is a BAM file with duplicate reads marked.
- A BED file of peaks called for alignments in the BAM file. Specify "auto" to use the BAM file name with ".peaks" appended, or if the BAM file contains read groups, to assume each read group has a peak file whose name is the read group ID with ".peaks" appended. If you specify a single filename instead of "auto" with read groups, the same peaks will be used for all reads -- be sure this is what you want.
- A BED file of transcription start sites for the experiment organism. If supplied, a TSS enrichment score will be calculated according to the ENCODE data standards. This calculation requires that the BAM file of alignments be indexed.
- If a TSS enrichment score is requested, it will be calculated for a region of "size" bases to either side of transcription start sites. The default is 1000bp.
- A BED file containing excluded regions. Peaks or TSS overlapping these will be ignored. May be given multiple times.
- The JSON file to which metrics will be written. The default filename will be based on the BAM file, with the suffix ".ataqv.json".
- If given, problematic reads will be logged to a file per read group, with names derived from the read group IDs, with ".problems" appended. If no read groups are found, the reads will be written to one file named after the BAM file.
- If given, output a subset of metrics that should be less redundant. If this flag is used, the same flag should be passed to mkarv when making the viewer.
- A label to be used for the metrics when there are no read groups. If there are read groups, each will have its metrics named using its ID field. With no read groups and no --name given, your metrics will be named after the alignment file.
- Even if read groups are present in the BAM file, ignore them and combine metrics for all reads under a single sample and library named with the --name option. This also implies that a single peak file will be used for all reads; see the --peak option.
- Data is single-nucleus, with the barcode stored in this BAM tag. In this case, metrics will be collected per barcode.
- A short description of the experiment.
- A URL for more detail on the experiment (perhaps using a DOI).
- Use this description for all libraries in the BAM file, instead of using the DS field from each read group.
- Organism
- Autosomal References
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- fly
- 2R 2L 3R 3L 4
- human
- 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22
- mouse
- 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19
- rat
- 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
- worm
- I II III IV V
- yeast
- I II III IV V VI VII VIII IX X XI XII XIII XIV XV XVI
- The default autosomal reference lists contain names with "chr" prefixes ("chr1") and without ("1"). If you need a different set of autosomes, you can supply a list with --autosomal-reference-file.
- A file containing autosomal reference names, one per line. The names must match the reference names in the alignment file exactly, or the metrics based on counts of autosomal alignments will be wrong.
- If the reference name for mitochondrial DNA in your alignment file is not "chrM",. use this option to supply the correct name. Again, if this name is wrong, all the measurements involving mitochondrial alignments will be wrong.
September 2022 | ataqv 1.3.0 |