Rsamtools: error with quickBamFlagSummary
0
1
Entering edit mode
6.4 years ago
bsmith030465 ▴ 240

Hi,

I was trying to determine if my bam file was single or pair ended. However, when I try to use Rsamtools, I get an error:

> quickBamFlagSummary(file="/Users/bsmith/Documents/run_s1_Aligned_Reads.bam")
Error: identical(length(N_1seg_rec_per_uqname) + length(N_mseg_rec_per_uqname),  .... is not TRUE

> traceback()

9: stop(msg, call. = FALSE, domain = NA)
8: stopifnot(identical(length(N_1seg_rec_per_uqname) + length(N_mseg_rec_per_uqname), 
   length(N_rec_per_uqname)))
7: quickBamFlagSummary(res0, param = param, main.groups.only = main.groups.only)
6: quickBamFlagSummary(res0, param = param, main.groups.only = main.groups.only)
5: quickBamFlagSummary(file, param = param, main.groups.only = main.groups.only)
4: quickBamFlagSummary(file, param = param, main.groups.only = main.groups.only)
3: .local(file, ..., param = param, main.groups.only = main.groups.only)
2: quickBamFlagSummary(file = "/Users/bsmith/Documents/run_s1_Aligned_Reads.bam")
1: quickBamFlagSummary(file = "/Users/bsmith/Documents/run_s1_Aligned_Reads.bam")

Is there something I need to do differently? Its a RNA seq data, if that helps any...

thanks!

Rsamtools RNA-Seq • 1.0k views
ADD COMMENT

Login before adding your answer.

Traffic: 2648 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