Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • ruoft
    Junior Member
    • May 2015
    • 5

    DiffBind error- bad magic number

    Hello everyone,
    I am having problems running diffbind count function. I keep getting the following error (running in R on Mac):

    > H3K9me3 = dba.count(H3K9me3, minOverlap=2)
    Error: Error processing one or more read files. Check warnings().
    In addition: Warning messages:
    1: In mclapply(arglist, fn, ..., mc.preschedule = TRUE, mc.allow.recursive = TRUE) :
    all scheduled cores encountered errors in user code
    2: file '~/Desktop/H3K9me3_bam/Wt1_H2K9me3_chip_sorted.bam.bam' does not appear to be a BAM file (bad magic number)

    I checked the numerical code at the end of my bam file and it appears to be correct:

    00029de0 7f 02 32 f0 24 b6 00 ed 00 00 1f 8b 08 04 00 00 |..2.$...........|
    00029df0 00 00 00 ff 06 00 42 43 02 00 1b 00 03 00 00 00 |......BC........|
    00029e00 00 00 00 00 00 00 |......|
    00029e06

    I have sorted and resorted with sam tools with no change. The bam file works fine for loading into IGV and such, so it is not unreadable. Any ideas?

    Thanks so much!
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    This is presumably referring to the magic number* at the beginning of the file, which is "BAM\1". If that's there then this is likely a bug in diffbind. What version are you using (just post the output of sessionInfo()).

    *Well, "magic string"

    Comment

    • rory
      Member
      • Aug 2008
      • 28

      #3
      If you could re-post this issue to the Bioconductor support site:
      https://support.bioconductor.org/'

      we can address this there. Please do include the sessionInfo() output.

      The way you are using dba.count(), without using the summits parameter, there is a workaround you can try. If you set bUseSummarizeOverlaps=TRUE, a different method will be used to access the bam files and that might work (let us know if it does in support post).

      Cheers-
      Rory

      Comment

      • ruoft
        Junior Member
        • May 2015
        • 5

        #4
        Hello,

        Thank you so much for the responses. I did try the "bUseSummarizeOverlaps=TRUE" addition to the count function and that appears to have fixed the problem. :-) Thanks so much!


        The session info is as follows:

        R version 3.2.2 (2015-08-14)
        Platform: x86_64-apple-darwin13.4.0 (64-bit)
        Running under: OS X 10.10.3 (Yosemite)

        locale:
        [1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

        attached base packages:
        [1] stats4 parallel stats graphics grDevices utils
        [7] datasets methods base

        other attached packages:
        [1] DiffBind_1.14.6 RSQLite_1.0.0
        [3] DBI_0.3.1 locfit_1.5-9.1
        [5] GenomicAlignments_1.4.1 Rsamtools_1.20.4
        [7] Biostrings_2.36.4 XVector_0.8.0
        [9] limma_3.24.15 GenomicRanges_1.20.8
        [11] GenomeInfoDb_1.4.3 IRanges_2.2.7
        [13] S4Vectors_0.6.6 BiocGenerics_0.14.0
        [15] BiocInstaller_1.18.4

        loaded via a namespace (and not attached):
        [1] Rcpp_0.12.1 lattice_0.20-33
        [3] GO.db_3.1.2 gtools_3.5.0
        [5] digest_0.6.8 plyr_1.8.3
        [7] futile.options_1.0.0 BatchJobs_1.6
        [9] ShortRead_1.26.0 ggplot2_1.0.1
        [11] gplots_2.17.0 zlibbioc_1.14.0
        [13] annotate_1.46.1 gdata_2.17.0
        [15] Matrix_1.2-2 checkmate_1.6.2
        [17] systemPipeR_1.2.23 proto_0.3-10
        [19] GOstats_2.34.0 splines_3.2.2
        [21] BiocParallel_1.2.21 stringr_1.0.0
        [23] pheatmap_1.0.7 munsell_0.4.2
        [25] sendmailR_1.2-1 base64enc_0.1-3
        [27] BBmisc_1.9 fail_1.2
        [29] edgeR_3.10.2 XML_3.98-1.3
        [31] AnnotationForge_1.10.1 MASS_7.3-44
        [33] bitops_1.0-6 grid_3.2.2
        [35] RBGL_1.44.0 xtable_1.7-4
        [37] GSEABase_1.30.2 gtable_0.1.2
        [39] magrittr_1.5 scales_0.3.0
        [41] graph_1.46.0 KernSmooth_2.23-15
        [43] amap_0.8-14 stringi_0.5-5
        [45] hwriter_1.3.2 reshape2_1.4.1
        [47] genefilter_1.50.0 latticeExtra_0.6-26
        [49] futile.logger_1.4.1 brew_1.0-6
        [51] rjson_0.2.15 lambda.r_1.1.7
        [53] RColorBrewer_1.1-2 tools_3.2.2
        [55] Biobase_2.28.0 Category_2.34.2
        [57] survival_2.38-3 AnnotationDbi_1.30.1
        [59] colorspace_1.2-6 caTools_1.17.1

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by SEQadmin2


          I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

          Here are nine questions we think about, in roughly the order they matter, before...
          06-18-2026, 07:11 AM
        • SEQadmin2
          From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
          by SEQadmin2


          Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


          The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
          ...
          06-02-2026, 10:05 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 05:37 AM
        0 responses
        6 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-26-2026, 11:10 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-17-2026, 06:09 AM
        0 responses
        51 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-09-2026, 11:58 AM
        0 responses
        110 views
        0 reactions
        Last Post SEQadmin2  
        Working...