Entering edit mode
gleuzzi.gl
•
0
@gleuzzigl-23377
Last seen 4.6 years ago
Hi all,
I am new person in NGS analysis. I am using ATACseqQC as suggest in the tutorial pubblished recently April 2020 to asses my ATAC-seq data.
In terestingly I found that when I use the following code across all my BAM files, it returns always with the same tags.
possibleTag <- combn(LETTERS, 2)
possibleTag <- c(paste0(possibleTag[1, ], possibleTag[2, ]),
paste0(possibleTag[2, ], possibleTag[1, ]))
library(Rsamtools)
bamTop100 <- scanBam(BamFile(bamfile, yieldSize = 100),
param = ScanBamParam(tag=possibleTag))[[1]]$tag
tags <- names(bamTop100)[lengths(bamTop100) == 100]
tags
[1] "PG" "YT"
[1] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[6] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[11] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[16] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[21] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[26] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[31] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[36] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[41] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[46] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[51] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[56] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[61] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[66] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[71] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[76] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[81] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[86] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[91] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
[96] "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates" "MarkDuplicates"
>
Any suggestions?
I really appreciate any help. Thanks a lot
Hi,
Could you use samtools to show the top 10 lines of your bam file like this: