Hello everyone!
I want to analyze my PAR-CLIP data utilizing wavClusteR. So when I try to create count table from my bam file (prepared by CLC WB) by command below
countTable <- getAllSub( Bam, minCov = 10 )
I have the error like that:
Error in { :
task 1 failed - "solving row 140: range cannot be determined from the supplied arguments (too many NAs)"
My bam:
> Bam
GRanges object with 872714 ranges and 2 metadata columns:
seqnames ranges strand | qseq MD
<Rle> <IRanges> <Rle> | <DNAStringSet> <character>
[1] chr1 [ 57283, 57298] + | CAGTCATTCCGAACAA 16
[2] chr1 [ 57283, 57298] - | CAGTCATTCCGAACAA 16
[3] chr1 [612758, 612776] + | CCGGAGGCTGAGGTGGGAG 19
[4] chr1 [612758, 612776] - | CCGGAGGCTGAGGTGGGAG 19
[5] chr1 [629167, 629204] + | ATTATTATAA...CAATCTTCCT 19T18
... ... ... ... . ... ...
[872710] KI270751.1 [39996, 40045] - | CAGGTCGCTG...AGAAAGGGAC 50
[872711] KI270751.1 [64988, 65049] + | TTTCTGACCT...AGACGTAAAC 55A6
[872712] KI270751.1 [64988, 65049] - | TTTCTGACCT...AGACGTAAAC 55A6
[872713] KI270756.1 [45603, 45618] + | TCCGTTCCACTTTATT 9T6
[872714] KI270756.1 [45603, 45618] - | TCCGTTCCACTTTATT 9T6
-------
seqinfo: 524 sequences from an unspecified genome; no seqlengths
I tried to realignment my fastq files using Tophat2, Bowtie2 nevetheless I have the same error.
Can you recommend the align tools and the exact parameters I need to use to get acceptable for wavClusteR bam files.
Thank you in advance,
Alexandr Gopanenko