ATACseqQC and Rsamtools scanBam
0
0
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

software error • 587 views
ADD COMMENT
0
Entering edit mode

Hi,

Could you use samtools to show the top 10 lines of your bam file like this:

 samtools view path/to/your/bam | head -n 10
ADD REPLY

Login before adding your answer.

Traffic: 863 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6