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3.9 years ago
shrinka.genetics
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I am working on WGBS Data and using MethyKIt package. When I used 8 samples in groups, it worked fine. Now on another set of data, where just 1 sample in each group is there. Here I am facing a problem
myDiff=calculateDiffMeth(meth,mc.cores=2) two groups detected: will calculate methylation difference as the difference of treatment (group: 1) - control (group: 0)
NOTE: performing 'fast.fisher' instead of 'F' for two groups testing. Error in mclapply(cntlist, function(x) fast.fisher(matrix(as.numeric(x), : 'mc.cores' > 1 is not supported on Windows
How can I correct this error? So that in later steps which is working on the object myDiff can be obtained.
Regards Shrinka
then don't use Windows, run you R code in a Linux machine or use Docker
Thanks for your tip. I have done it as I put mc.cores=1, It worked.
after that step I am getting another error. Any clue how to solve this?
> annotateWithGeneParts(as(myDiff25p,"GRanges"),gene.obj)
Error in NSBS(i, x, exact = exact, strict.upper.bound = !allow.append, : subscript contains NAs In addition: Warning messages: 1: In .Seqinfo.mergexy(x, y) : The 2 combined objects have no sequence levels in common. (Use suppressWarnings() to suppress this warning.) 2: In .Seqinfo.mergexy(x, y) : The 2 combined objects have no sequence levels in common. (Use suppressWarnings() to suppress this warning.) 3: In .Seqinfo.mergexy(x, y) : The 2 combined objects have no sequence levels in common. (Use suppressWarnings() to suppress this warning.) 4: In .Seqinfo.mergexy(x, y) : The 2 combined objects have no sequence levels in common. (Use suppressWarnings() to suppress this warning.) 5: In .Seqinfo.mergexy(x, y) : The 2 combined objects have no sequence levels in common. (Use suppressWarnings() to suppress this warning.) 6: In .Seqinfo.mergexy(x, y) : The 2 combined objects have no sequence levels in common. (Use suppressWarnings() to suppress this warning.)
Thanks Shrinka
check the contig/chromosome names (for eg. chr1 vs 1 or contig 1 vs 1) in bed and cpg files used.
Sorry, not understood, where should I check this?
how did you create
gene.obj? Print few lines frommyDiff25pobject.Hello I made gene.obj by using this command, where "refseq.hg18.bed.txt" file is there with MethyKit package
gene.obj<-readTranscriptFeatures("refseq.hg18.bed.txt")
Regards
Shrinka
Post few lines from
mydiff25pobject andrefseq.hg18.bed.txt@ shrinka.geneticsHere are these. PFA first 10 lines of refseq.hg18.bed.txt file.
methylDiff object with 6 rows
385 21 9483774 9483774 + 4.462922e-04 0.0068459260 -45.83333 1032 21 9656103 9656103 + 4.325999e-04 0.0066740425 25.85200 1220 21 9674182 9674182 + 4.919951e-06 0.0001579141 38.53448 1298 21 9679300 9679300 + 1.461574e-04 0.0027225173 -48.14815 1597 21 9753103 9753103 + 2.995814e-05 0.0007255432 77.27273
1898 21 9826814 9826814 + 2.030031e-04 0.0035856587 -36.45594
sample.ids: delta21-mod gamma21-mod destranded FALSE assembly: hg18 context: CpG treament: 1 0 resolution: base [1] 11082 7 GRangesList object of length 4: $exons GRanges object with 22359 ranges and 2 metadata columns: seqnames ranges strand | score name <rle> <iranges> <rle> | <numeric> <character> [1] chr20 33506637-33506986 + | 1 NM_007186 [2] chr20 33509539-33509609 + | 2 NM_007186 [3] chr20 33511217-33511339 + | 3 NM_007186 [4] chr20 33513504-33513792 + | 4 NM_007186 [5] chr20 33514814-33514870 + | 5 NM_007186 ... ... ... ... . ... ... [22355] chr22 49561066-49561145 - | 5 NM_001130922 [22356] chr22 49561964-49562043 - | 4 NM_001130922 [22357] chr22 49563246-49563275 - | 3 NM_001130922 [22358] chr22 49567482-49567645 - | 2 NM_001130922 [22359] chr22 49568795-49568953 - | 1 NM_001130922
seqinfo: 3 sequences from an unspecified genome; no seqlengths
... <3 more elements>
I am clueless why the dimension is showing NULL NULL
Regards Shrinka
I see that
methyldiffobject has chromosome is represented by "21" (ti.e without word "chr") where as bed file (refseq.hg18.bed.txt) seems to have "chr" appended to chromosome name. Remove "chr" from the chromosome names of the bed file and recreategene.objand the run the code again.Formatting of your post is confusing and Please format the data for better understanding.
ok, how will I do that? by what command?
Regards Shrinka
On GNU-linux machine,
Use
refseq.hg18.modified.bed.txt, for building gene.obj.Btw, if you are using refseq.hg18.bed.txt from methylkit package, you must know that it is truncated bed file. Are you using this bed.txt for your work or for reproducing methylkit tutorial?
Hello I am using this bed file for my work, to analyse my data.
Thanks Shrinka
Before I comment further, could you please post the source of the bed.txt file?
I can attach it off course. I mentioned It comes with Methylkit package itself. It is in exdata folder of that package only.
Thanks Shrinka
That bed.txt file has only these chromosomes: chr20, chr21, chr22, chr21_random, chr22_random, chr22_h2_hap1. Full bed file (with all main chromosomes) is supposed to be used in the analysis, instead of truncated bed file (meant for a tutorial only) unless you are looking for DMRs in chr 20,21 and 22 only. Btw, for alignment, did you use bismark? if so, which genome fasta you have used?
No I have not used bismark, as my input file was in matrix form, text file.
Thanks Shrinka
Thanks, I will work on that and will keep posting here.
What do you mean by text matrix?
Regards Shrinka
as my input file was in matrix form, text file..this fileYes it worked
Thanks Shrinka