error when I use groHMM on data outside of the tutorial
0
1
Entering edit mode
Deleted ▴ 70
@jsalsager-14698
Last seen 11 months ago
United States

Hi,

When I tried the groHMM package tutorial, I was able to get everything to work. When I try it with real data, I keep getting this error "the score must be numeric, without any NA's". I appreciate any help because I have been searching the internet and trying to figure this out on my own for several days. 

For data processing, I used cutadapt to remove adapters and low quality reads. I aligned to hg19 with bwa, and coverted the resulting sam file to a bam file with samtools. When I load it into R for groHMM analysis, this is what happens:

 

> SRR5364056 <- as(readGAlignments("SRR5364056.bam"), "GRanges")
> writeWiggle(reads=SRR5364056, file="SRR5364056_Plus.wig", fileType="wig", strand="+",
+ reverse=FALSE)
Error in .local(object, con, format, ...) : 
  The score must be numeric, without any NA's
In addition: Warning messages:
1: In mclapply(readsList, function(x) { :
  all scheduled cores encountered errors in user code
2: In DataFrame(..., check.names = FALSE) : NAs introduced by coercion
> writeWiggle(reads=SRR5364056, file="SRR5364056_Minus.wig", fileType="wig", strand="-",
+ reverse=TRUE)
Error in .local(object, con, format, ...) : 
  The score must be numeric, without any NA's
In addition: Warning messages:
1: In mclapply(readsList, function(x) { :
  all scheduled cores encountered errors in user code
2: In DataFrame(..., check.names = FALSE) : NAs introduced by coercion

> sessionInfo()
R version 3.5.1 (2018-07-02)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: Ubuntu 16.04.5 LTS

Matrix products: default
BLAS: /usr/lib/libblas/libblas.so.3.6.0
LAPACK: /usr/lib/lapack/liblapack.so.3.6.0

locale:
 [1] LC_CTYPE=en_US.UTF-8       LC_NUMERIC=C              
 [3] LC_TIME=en_US.UTF-8        LC_COLLATE=en_US.UTF-8    
 [5] LC_MONETARY=en_US.UTF-8    LC_MESSAGES=en_US.UTF-8   
 [7] LC_PAPER=en_US.UTF-8       LC_NAME=C                 
 [9] LC_ADDRESS=C               LC_TELEPHONE=C            
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C       

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

other attached packages:
 [1] groHMM_1.14.0               rtracklayer_1.40.6         
 [3] GenomicAlignments_1.16.0    Rsamtools_1.32.3           
 [5] Biostrings_2.48.0           XVector_0.20.0             
 [7] SummarizedExperiment_1.10.1 DelayedArray_0.6.5         
 [9] BiocParallel_1.14.2         matrixStats_0.54.0         
[11] Biobase_2.40.0              GenomicRanges_1.32.6       
[13] GenomeInfoDb_1.16.0         IRanges_2.14.11            
[15] S4Vectors_0.18.3            BiocGenerics_0.26.0        
[17] MASS_7.3-50                

loaded via a namespace (and not attached):
 [1] zlibbioc_1.26.0        lattice_0.20-35        tools_3.5.1           
 [4] grid_3.5.1             Matrix_1.2-14          GenomeInfoDbData_1.1.0
 [7] bitops_1.0-6           RCurl_1.95-4.11        compiler_3.5.1        
[10] XML_3.98-1.16         
> SRR5364056
GRanges object with 18253707 ranges and 0 metadata columns:
             seqnames            ranges strand
                <Rle>         <IRanges>  <Rle>
         [1]    chr10       67286-67336      +
         [2]    chr10       82341-82391      +
         [3]    chr10       84427-84477      +
         [4]    chr10       84434-84484      +
         [5]    chr10       84564-84614      +
         ...      ...               ...    ...
  [18253703]     chrY 59360648-59360698      +
  [18253704]     chrY 59360705-59360755      +
  [18253705]     chrY 59360705-59360755      +
  [18253706]     chrY 59360705-59360755      +
  [18253707]     chrY 59360706-59360756      +
  -------
  seqinfo: 93 sequences from an unspecified genome
> 

 

Thanks a million! 

grohmm groseq next-generation sequencing R • 1.4k views
ADD COMMENT
2
Entering edit mode

Hello,

Can you try including just the standard chromosomes and then execute the writeWiggle step

gr <- keepStandardChromosomes(SRR5364056)

or if you are using  R 3.4.4

gr <- keepStandardChromosomes(SRR5364056, pruning.mode="coarse")

 

 

 

ADD REPLY
0
Entering edit mode

THANK YOU!!!!!!!

ADD REPLY

Login before adding your answer.

Traffic: 550 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