seqsumm_out.txt.
runSeqsumm(summ.win=50, file=NULL, folder=NULL, output.file="seqsumm_out.txt", samtools.path="samtools")readSeqsumm will look for seqsumm_out.txt.
seqsumm_out.txt (or the indicated name), which will be read by the function readSeqsumm, is generated in the indicated folder. Therefore, you only need to call this function once, unless you want to generate a new file with other input/parameters.
The output file has chromosome, window, mean GC and mean mapping quality columns, and either a count column for single-end alignments or five count columns for paired-end alignments:
- Type 1. Mapped with correct orientation and within insert size.
- Type 2. Mapped with correct orientation and uniquely, but wrong insert size.
- Type 3. Mapped within the insert size but wrong orientation.
- Type 4. Mapped uniquely, but wrong orientation and insert size.
- Type 5. One of the mates in unmapped.
See seqsumm_HCC1143 for an example table generated by the function.
The function does not return anything.
file.copy(file.path(system.file(package="seqCNA"), "extdata/test.sam"), tempdir())
tempdir()
window.size = 50
runSeqsumm(window.size, folder=tempdir())
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