export Views of Rle in rtracklayer
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jason0701 ▴ 190
@jason0701-3921
Last seen 5.0 years ago
Hi list, I have a question and would like to get your help. What I would like to get is to show the read coverage in the exon regions (only) in the ucsc genome browser. My question is how to export the Views so I can load into ucsc browser. Here is what I have: # >cvg = coverage(ranges(ss)) >cvg.view = Views(cvg,rangesexon.gr)) # exon.gr is a GRanges >cvg.view Views on a 22109556-length Rle subject views: start end width [1] 22109317 22109688 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 9 9 9 ...] [2] 22084156 22084276 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 4 4 4 ...] [3] 22083039 22083195 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 3 3 4 ...] [4] 22079485 22079612 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 2 2 2 ...] [5] 22079020 22079144 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 6 5 4 ...] I don't know how to modify this view such as adding chromosome info and export this 'cvg.view' in rtracklayer. Thanks in advance. Jason > sessionInfo() R version 2.14.0 (2011-10-31) Platform: x86_64-unknown-linux-gnu (64-bit) locale: [1] C attached base packages: [1] stats graphics grDevices utils datasets methods base other attached packages: [1] rtracklayer_1.14.3 RCurl_1.7-0 bitops_1.0-4.1 [4] Rsamtools_1.6.2 Biostrings_2.22.0 GenomicFeatures_1.6.4 [7] AnnotationDbi_1.16.4 Biobase_2.14.0 GenomicRanges_1.6.3 [10] IRanges_1.12.2 BiocInstaller_1.2.1 loaded via a namespace (and not attached): [1] BSgenome_1.22.0 DBI_0.2-5 RSQLite_0.10.0 XML_3.4-3 [5] biomaRt_2.10.0 tools_2.14.0 zlibbioc_1.0.0 >
Coverage rtracklayer Coverage rtracklayer • 1.6k views
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@martin-morgan-1513
Last seen 4 months ago
United States
On 11/22/2011 09:39 AM, Jason Lu wrote: > Hi list, > > I have a question and would like to get your help. > What I would like to get is to show the read coverage in the exon > regions (only) in the ucsc genome browser. My question is how to > export the Views so I can load into ucsc browser. > Here is what I have: > > # >> cvg = coverage(ranges(ss)) >> cvg.view = Views(cvg,rangesexon.gr)) # exon.gr is a GRanges >> cvg.view > Views on a 22109556-length Rle subject > > views: > start end width > [1] 22109317 22109688 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 9 9 9 ...] > [2] 22084156 22084276 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 4 4 4 ...] > [3] 22083039 22083195 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 3 3 4 ...] > [4] 22079485 22079612 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 2 2 2 ...] > [5] 22079020 22079144 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 6 5 4 ...] > > I don't know how to modify this view such as adding chromosome info > and export this 'cvg.view' in rtracklayer. Hi Jason -- not my strength, but I think you can fl <- paste(tempfile(), "gff", sep=".") export(ranges(cvg.view), fl) at a minimum, or add annotations through arguments to specific export functions (e.g., ?export.gff) or creating a richer object, e.g., RangedData(ranges(cvf.view), space="chr1") Hope that helps, and is not too misleading, Martin > Thanks in advance. > Jason > >> sessionInfo() > R version 2.14.0 (2011-10-31) > Platform: x86_64-unknown-linux-gnu (64-bit) > > locale: > [1] C > > attached base packages: > [1] stats graphics grDevices utils datasets methods base > > other attached packages: > [1] rtracklayer_1.14.3 RCurl_1.7-0 bitops_1.0-4.1 > [4] Rsamtools_1.6.2 Biostrings_2.22.0 GenomicFeatures_1.6.4 > [7] AnnotationDbi_1.16.4 Biobase_2.14.0 GenomicRanges_1.6.3 > [10] IRanges_1.12.2 BiocInstaller_1.2.1 > > loaded via a namespace (and not attached): > [1] BSgenome_1.22.0 DBI_0.2-5 RSQLite_0.10.0 XML_3.4-3 > [5] biomaRt_2.10.0 tools_2.14.0 zlibbioc_1.0.0 >> > > _______________________________________________ > Bioconductor mailing list > Bioconductor at r-project.org > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor -- Computational Biology Fred Hutchinson Cancer Research Center 1100 Fairview Ave. N. PO Box 19024 Seattle, WA 98109 Location: M1-B861 Telephone: 206 667-2793
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@michael-lawrence-3846
Last seen 3.0 years ago
United States
On Tue, Nov 22, 2011 at 9:39 AM, Jason Lu <jasonlu68@gmail.com> wrote: > Hi list, > > I have a question and would like to get your help. > What I would like to get is to show the read coverage in the exon > regions (only) in the ucsc genome browser. My question is how to > export the Views so I can load into ucsc browser. > Here is what I have: > > # > >cvg = coverage(ranges(ss)) > Careful here: you are not distinguishing chromosomes when calculating this coverage. It's all going into one vector. Instead, you want to call coverage directly on your GRanges 'ss'. cvg <- coverage(ss) > >cvg.view = Views(cvg,rangesexon.gr)) # exon.gr is a GRanges > Since 'cvg' is now an RleList (with one element per chromosome), you want a RangesList to parallel it in your RleViewsList. cvg.view <- Views(cvg, asexon.gr, "RangesList")) I think we should try to make that easier and have Views() take a GRanges. Will make a note. > >cvg.view > Views on a 22109556-length Rle subject > > views: > start end width > [1] 22109317 22109688 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 9 9 9 > ...] > [2] 22084156 22084276 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 4 4 4 > ...] > [3] 22083039 22083195 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 3 3 4 > ...] > [4] 22079485 22079612 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 2 2 2 > ...] > [5] 22079020 22079144 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 6 5 4 > ...] > > I don't know how to modify this view such as adding chromosome info > and export this 'cvg.view' in rtracklayer. > You can now export this RleViewsList directly to a file for upload. For upload to the UCSC browser, how about: session <- browserSession() session$coverage <- cvg.view browserView(session, exon.gr[1]) That should show you the first exon. Thanks in advance. > Jason > > > sessionInfo() > R version 2.14.0 (2011-10-31) > Platform: x86_64-unknown-linux-gnu (64-bit) > > locale: > [1] C > > attached base packages: > [1] stats graphics grDevices utils datasets methods base > > other attached packages: > [1] rtracklayer_1.14.3 RCurl_1.7-0 bitops_1.0-4.1 > [4] Rsamtools_1.6.2 Biostrings_2.22.0 GenomicFeatures_1.6.4 > [7] AnnotationDbi_1.16.4 Biobase_2.14.0 GenomicRanges_1.6.3 > [10] IRanges_1.12.2 BiocInstaller_1.2.1 > > loaded via a namespace (and not attached): > [1] BSgenome_1.22.0 DBI_0.2-5 RSQLite_0.10.0 XML_3.4-3 > [5] biomaRt_2.10.0 tools_2.14.0 zlibbioc_1.0.0 > > > > _______________________________________________ > Bioconductor mailing list > Bioconductor@r-project.org > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: > http://news.gmane.org/gmane.science.biology.informatics.conductor > [[alternative HTML version deleted]]
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I want to thank Michael and Martin for being helpful. My apology for not showing the full script last email. The purpose here is to get a figure showing read coverage in the exon regions of my gene of interest (one gene). I tried some additional steps here and get an error below. # nm = "NM_000997" txs = exonsBy(txdb,by="tx",use.name=TRUE) toshow = txs[[nm]] ss <- readBamGappedAlignments("myalign.bam",param=ScanBamParam(which=t oshow)) strand(ss) = "*" cvg = coverage(ss) # cvg: SimpleRleList cvg.view <- Views(cvg, as(toshow, "RangesList")) Error in .Method(..., FUN = FUN, MoreArgs = MoreArgs, SIMPLIFY = SIMPLIFY, : all object lengths must be multiple of longest object length Also, I have been unsuccessful in exporting the RleViewsList to a file (wig or bedGraph format). Could you give a hint on this as well? Thanks again. Jason On Wed, Nov 23, 2011 at 8:20 AM, Michael Lawrence <lawrence.michael at="" gene.com=""> wrote: > > > On Tue, Nov 22, 2011 at 9:39 AM, Jason Lu <jasonlu68 at="" gmail.com=""> wrote: >> >> Hi list, >> >> I have a question and would like to get your help. >> What I would like to get is to show the read coverage in the exon >> regions (only) in the ucsc genome browser. My question is how to >> export the Views so I can load into ucsc browser. >> Here is what I have: >> >> # >> >cvg = coverage(ranges(ss)) > > Careful here: you are not distinguishing chromosomes when calculating this > coverage. It's all going into one vector. Instead, you want to call coverage > directly on your GRanges 'ss'. > > cvg <- coverage(ss) > >> >> >cvg.view = Views(cvg,rangesexon.gr)) ?# exon.gr is a GRanges > > Since 'cvg' is now an RleList (with one element per chromosome), you want a > RangesList to parallel it in your RleViewsList. > > cvg.view <- Views(cvg, asexon.gr, "RangesList")) > > I think we should try to make that easier and have Views() take a GRanges. > Will make a note. > >> >> >cvg.view >> Views on a 22109556-length Rle subject >> >> views: >> ? ? ? ?start ? ? ?end width >> ?[1] 22109317 22109688 ? 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 9 9 9 >> ...] >> ?[2] 22084156 22084276 ? 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 4 4 4 >> ...] >> ?[3] 22083039 22083195 ? 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 3 3 4 >> ...] >> ?[4] 22079485 22079612 ? 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 2 2 2 >> ...] >> ?[5] 22079020 22079144 ? 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 6 5 4 >> ...] >> >> I don't know how to modify this view such as adding chromosome info >> and export this 'cvg.view' in rtracklayer. > > > You can now export this RleViewsList directly to a file for upload. For > upload to the UCSC browser, how about: > > session <- browserSession() > session$coverage <- cvg.view > browserView(session, exon.gr[1]) > > That should show you the first exon. > >> Thanks in advance. >> Jason >> >> > sessionInfo() >> R version 2.14.0 (2011-10-31) >> Platform: x86_64-unknown-linux-gnu (64-bit) >> >> locale: >> [1] C >> >> attached base packages: >> [1] stats ? ? graphics ?grDevices utils ? ? datasets ?methods ? base >> >> other attached packages: >> ?[1] rtracklayer_1.14.3 ? ?RCurl_1.7-0 ? ? ? ? ? bitops_1.0-4.1 >> ?[4] Rsamtools_1.6.2 ? ? ? Biostrings_2.22.0 ? ? GenomicFeatures_1.6.4 >> ?[7] AnnotationDbi_1.16.4 ?Biobase_2.14.0 ? ? ? ?GenomicRanges_1.6.3 >> [10] IRanges_1.12.2 ? ? ? ?BiocInstaller_1.2.1 >> >> loaded via a namespace (and not attached): >> [1] BSgenome_1.22.0 DBI_0.2-5 ? ? ? RSQLite_0.10.0 ?XML_3.4-3 >> [5] biomaRt_2.10.0 ?tools_2.14.0 ? ?zlibbioc_1.0.0 >> > >> >> _______________________________________________ >> Bioconductor mailing list >> Bioconductor at r-project.org >> https://stat.ethz.ch/mailman/listinfo/bioconductor >> Search the archives: >> http://news.gmane.org/gmane.science.biology.informatics.conductor > >
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On Wed, Nov 23, 2011 at 7:18 AM, Jason Lu <jasonlu68@gmail.com> wrote: > I want to thank Michael and Martin for being helpful. > > My apology for not showing the full script last email. The purpose > here is to get a figure showing read coverage in the exon regions of > my gene of interest (one gene). I tried some additional steps here and > get an error below. > > # > nm = "NM_000997" > txs = exonsBy(txdb,by="tx",use.name=TRUE) > toshow = txs[[nm]] > ss <- > readBamGappedAlignments("myalign.bam",param=ScanBamParam(which=tosho w)) > strand(ss) = "*" > cvg = coverage(ss) # cvg: SimpleRleList > > cvg.view <- Views(cvg, as(toshow, "RangesList")) > Error in .Method(..., FUN = FUN, MoreArgs = MoreArgs, SIMPLIFY = SIMPLIFY, > : > all object lengths must be multiple of longest object length > > The problem here is likely that "toshow" is on a wider universe (set of sequences) than your coverage vector from the BAM file. You can use keepSeqlevels(toshow, seqlevels(ss)). You want to make sure the seqlevels are in the same order; not sure if keepSeqlevels() does this -- perhaps it should? > Also, I have been unsuccessful in exporting the RleViewsList to a file > (wig or bedGraph format). Could you give a hint on this as well? > Thanks again. > > Now that I think about it, Views are a bit of an overkill for this specific case. You could just do a cvg.select <- seqselect(cvg, as(toshow, "RangesList")) And then export that: export(cvg.select, "coverage.bedGraph") Jason > > > On Wed, Nov 23, 2011 at 8:20 AM, Michael Lawrence > <lawrence.michael@gene.com> wrote: > > > > > > On Tue, Nov 22, 2011 at 9:39 AM, Jason Lu <jasonlu68@gmail.com> wrote: > >> > >> Hi list, > >> > >> I have a question and would like to get your help. > >> What I would like to get is to show the read coverage in the exon > >> regions (only) in the ucsc genome browser. My question is how to > >> export the Views so I can load into ucsc browser. > >> Here is what I have: > >> > >> # > >> >cvg = coverage(ranges(ss)) > > > > Careful here: you are not distinguishing chromosomes when calculating > this > > coverage. It's all going into one vector. Instead, you want to call > coverage > > directly on your GRanges 'ss'. > > > > cvg <- coverage(ss) > > > >> > >> >cvg.view = Views(cvg,rangesexon.gr)) # exon.gr is a GRanges > > > > Since 'cvg' is now an RleList (with one element per chromosome), you > want a > > RangesList to parallel it in your RleViewsList. > > > > cvg.view <- Views(cvg, asexon.gr, "RangesList")) > > > > I think we should try to make that easier and have Views() take a > GRanges. > > Will make a note. > > > >> > >> >cvg.view > >> Views on a 22109556-length Rle subject > >> > >> views: > >> start end width > >> [1] 22109317 22109688 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 9 9 > 9 > >> ...] > >> [2] 22084156 22084276 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 4 4 > 4 > >> ...] > >> [3] 22083039 22083195 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 3 3 > 4 > >> ...] > >> [4] 22079485 22079612 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 2 2 > 2 > >> ...] > >> [5] 22079020 22079144 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 6 5 > 4 > >> ...] > >> > >> I don't know how to modify this view such as adding chromosome info > >> and export this 'cvg.view' in rtracklayer. > > > > > > You can now export this RleViewsList directly to a file for upload. For > > upload to the UCSC browser, how about: > > > > session <- browserSession() > > session$coverage <- cvg.view > > browserView(session, exon.gr[1]) > > > > That should show you the first exon. > > > >> Thanks in advance. > >> Jason > >> > >> > sessionInfo() > >> R version 2.14.0 (2011-10-31) > >> Platform: x86_64-unknown-linux-gnu (64-bit) > >> > >> locale: > >> [1] C > >> > >> attached base packages: > >> [1] stats graphics grDevices utils datasets methods base > >> > >> other attached packages: > >> [1] rtracklayer_1.14.3 RCurl_1.7-0 bitops_1.0-4.1 > >> [4] Rsamtools_1.6.2 Biostrings_2.22.0 GenomicFeatures_1.6.4 > >> [7] AnnotationDbi_1.16.4 Biobase_2.14.0 GenomicRanges_1.6.3 > >> [10] IRanges_1.12.2 BiocInstaller_1.2.1 > >> > >> loaded via a namespace (and not attached): > >> [1] BSgenome_1.22.0 DBI_0.2-5 RSQLite_0.10.0 XML_3.4-3 > >> [5] biomaRt_2.10.0 tools_2.14.0 zlibbioc_1.0.0 > >> > > >> > >> _______________________________________________ > >> Bioconductor mailing list > >> Bioconductor@r-project.org > >> https://stat.ethz.ch/mailman/listinfo/bioconductor > >> Search the archives: > >> http://news.gmane.org/gmane.science.biology.informatics.conductor > > > > > [[alternative HTML version deleted]]
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Hi Michael, Thanks for the quick response. I tried the keepSeqlevels and your solution using the seqselect. It works! The only caveat is that the genomic coordinates are lost in the bedGraph. Here is what I have tried # toshow = keepSeqlevels(toshow,seqlevels(ss)) cvg = coverage(ss) cvg.select=seqselect(cvg,as(toshow,"RangesList")) export(cvg.select,"test.bedGraph") # output of test.bedGraph [genomic coordinates were lost] track name="R Track" type=bedGraph chr5 0 103 0 chr5 103 104 71 chr5 104 105 72 chr5 105 106 74 chr5 106 109 76 chr5 109 110 77 I may need to do shift with each exon start positions, or you may have more elegant solutions. Thanks. Jason On Wed, Nov 23, 2011 at 11:38 AM, Michael Lawrence <lawrence.michael at="" gene.com=""> wrote: > > > On Wed, Nov 23, 2011 at 7:18 AM, Jason Lu <jasonlu68 at="" gmail.com=""> wrote: >> >> I want to thank Michael and Martin for being helpful. >> >> My apology for not showing the full script last email. The purpose >> here is to get a figure showing read coverage in the exon regions of >> my gene of interest (one gene). I tried some additional steps here and >> get an error below. >> >> # >> nm = "NM_000997" >> txs ?= exonsBy(txdb,by="tx",use.name=TRUE) >> toshow = txs[[nm]] >> ss <- >> readBamGappedAlignments("myalign.bam",param=ScanBamParam(which=tosh ow)) >> strand(ss) = "*" >> cvg ?= coverage(ss) ?# cvg: SimpleRleList >> >> cvg.view <- Views(cvg, as(toshow, "RangesList")) >> Error in .Method(..., FUN = FUN, MoreArgs = MoreArgs, SIMPLIFY = SIMPLIFY, >> ?: >> ?all object lengths must be multiple of longest object length >> > > The problem here is likely that "toshow" is on a wider universe (set of > sequences) than your coverage vector from the BAM file. You can use > keepSeqlevels(toshow, seqlevels(ss)). You want to make sure the seqlevels > are in the same order; not sure if keepSeqlevels() does this -- perhaps it > should? > >> >> Also, I have been unsuccessful in exporting the RleViewsList to a file >> (wig or bedGraph format). Could you give a hint on this as well? >> Thanks again. >> > > Now that I think about it, Views are a bit of an overkill for this specific > case. You could just do a > > cvg.select <- seqselect(cvg, as(toshow, "RangesList")) > > And then export that: > > export(cvg.select, "coverage.bedGraph") > >> Jason >> >> >> On Wed, Nov 23, 2011 at 8:20 AM, Michael Lawrence >> <lawrence.michael at="" gene.com=""> wrote: >> > >> > >> > On Tue, Nov 22, 2011 at 9:39 AM, Jason Lu <jasonlu68 at="" gmail.com=""> wrote: >> >> >> >> Hi list, >> >> >> >> I have a question and would like to get your help. >> >> What I would like to get is to show the read coverage in the exon >> >> regions (only) in the ucsc genome browser. My question is how to >> >> export the Views so I can load into ucsc browser. >> >> Here is what I have: >> >> >> >> # >> >> >cvg = coverage(ranges(ss)) >> > >> > Careful here: you are not distinguishing chromosomes when calculating >> > this >> > coverage. It's all going into one vector. Instead, you want to call >> > coverage >> > directly on your GRanges 'ss'. >> > >> > cvg <- coverage(ss) >> > >> >> >> >> >cvg.view = Views(cvg,rangesexon.gr)) ?# exon.gr is a GRanges >> > >> > Since 'cvg' is now an RleList (with one element per chromosome), you >> > want a >> > RangesList to parallel it in your RleViewsList. >> > >> > cvg.view <- Views(cvg, asexon.gr, "RangesList")) >> > >> > I think we should try to make that easier and have Views() take a >> > GRanges. >> > Will make a note. >> > >> >> >> >> >cvg.view >> >> Views on a 22109556-length Rle subject >> >> >> >> views: >> >> ? ? ? ?start ? ? ?end width >> >> ?[1] 22109317 22109688 ? 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 9 9 >> >> 9 >> >> ...] >> >> ?[2] 22084156 22084276 ? 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 4 4 >> >> 4 >> >> ...] >> >> ?[3] 22083039 22083195 ? 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 3 3 >> >> 4 >> >> ...] >> >> ?[4] 22079485 22079612 ? 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 2 2 >> >> 2 >> >> ...] >> >> ?[5] 22079020 22079144 ? 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 6 5 >> >> 4 >> >> ...] >> >> >> >> I don't know how to modify this view such as adding chromosome info >> >> and export this 'cvg.view' in rtracklayer. >> > >> > >> > You can now export this RleViewsList directly to a file for upload. For >> > upload to the UCSC browser, how about: >> > >> > session <- browserSession() >> > session$coverage <- cvg.view >> > browserView(session, exon.gr[1]) >> > >> > That should show you the first exon. >> > >> >> Thanks in advance. >> >> Jason >> >> >> >> > sessionInfo() >> >> R version 2.14.0 (2011-10-31) >> >> Platform: x86_64-unknown-linux-gnu (64-bit) >> >> >> >> locale: >> >> [1] C >> >> >> >> attached base packages: >> >> [1] stats ? ? graphics ?grDevices utils ? ? datasets ?methods ? base >> >> >> >> other attached packages: >> >> ?[1] rtracklayer_1.14.3 ? ?RCurl_1.7-0 ? ? ? ? ? bitops_1.0-4.1 >> >> ?[4] Rsamtools_1.6.2 ? ? ? Biostrings_2.22.0 ? ? GenomicFeatures_1.6.4 >> >> ?[7] AnnotationDbi_1.16.4 ?Biobase_2.14.0 ? ? ? ?GenomicRanges_1.6.3 >> >> [10] IRanges_1.12.2 ? ? ? ?BiocInstaller_1.2.1 >> >> >> >> loaded via a namespace (and not attached): >> >> [1] BSgenome_1.22.0 DBI_0.2-5 ? ? ? RSQLite_0.10.0 ?XML_3.4-3 >> >> [5] biomaRt_2.10.0 ?tools_2.14.0 ? ?zlibbioc_1.0.0 >> >> > >> >> >> >> _______________________________________________ >> >> Bioconductor mailing list >> >> Bioconductor at r-project.org >> >> https://stat.ethz.ch/mailman/listinfo/bioconductor >> >> Search the archives: >> >> http://news.gmane.org/gmane.science.biology.informatics.conductor >> > >> > > >
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At this point, cvg.select <- subsetByOverlaps(as(cvg, "GRanges"), toshow) Should work, but it is not very efficient. We just need a RleViewsList -> RangedData/GRanges coercion. On the TODO list. On Wed, Nov 23, 2011 at 9:35 AM, Jason Lu <jasonlu68@gmail.com> wrote: > Hi Michael, > > Thanks for the quick response. > I tried the keepSeqlevels and your solution using the seqselect. It > works! The only caveat is that the genomic coordinates are lost in > the bedGraph. Here is what I have tried > > # > toshow = keepSeqlevels(toshow,seqlevels(ss)) > cvg = coverage(ss) > cvg.select=seqselect(cvg,as(toshow,"RangesList")) > export(cvg.select,"test.bedGraph") > > # output of test.bedGraph [genomic coordinates were lost] > track name="R Track" type=bedGraph > chr5 0 103 0 > chr5 103 104 71 > chr5 104 105 72 > chr5 105 106 74 > chr5 106 109 76 > chr5 109 110 77 > > I may need to do shift with each exon start positions, or you may have > more elegant solutions. > Thanks. > > Jason > > > On Wed, Nov 23, 2011 at 11:38 AM, Michael Lawrence > <lawrence.michael@gene.com> wrote: > > > > > > On Wed, Nov 23, 2011 at 7:18 AM, Jason Lu <jasonlu68@gmail.com> wrote: > >> > >> I want to thank Michael and Martin for being helpful. > >> > >> My apology for not showing the full script last email. The purpose > >> here is to get a figure showing read coverage in the exon regions of > >> my gene of interest (one gene). I tried some additional steps here and > >> get an error below. > >> > >> # > >> nm = "NM_000997" > >> txs = exonsBy(txdb,by="tx",use.name=TRUE) > >> toshow = txs[[nm]] > >> ss <- > >> readBamGappedAlignments("myalign.bam",param=ScanBamParam(which=to show)) > >> strand(ss) = "*" > >> cvg = coverage(ss) # cvg: SimpleRleList > >> > >> cvg.view <- Views(cvg, as(toshow, "RangesList")) > >> Error in .Method(..., FUN = FUN, MoreArgs = MoreArgs, SIMPLIFY = > SIMPLIFY, > >> : > >> all object lengths must be multiple of longest object length > >> > > > > The problem here is likely that "toshow" is on a wider universe (set of > > sequences) than your coverage vector from the BAM file. You can use > > keepSeqlevels(toshow, seqlevels(ss)). You want to make sure the seqlevels > > are in the same order; not sure if keepSeqlevels() does this -- perhaps > it > > should? > > > >> > >> Also, I have been unsuccessful in exporting the RleViewsList to a file > >> (wig or bedGraph format). Could you give a hint on this as well? > >> Thanks again. > >> > > > > Now that I think about it, Views are a bit of an overkill for this > specific > > case. You could just do a > > > > cvg.select <- seqselect(cvg, as(toshow, "RangesList")) > > > > And then export that: > > > > export(cvg.select, "coverage.bedGraph") > > > >> Jason > >> > >> > >> On Wed, Nov 23, 2011 at 8:20 AM, Michael Lawrence > >> <lawrence.michael@gene.com> wrote: > >> > > >> > > >> > On Tue, Nov 22, 2011 at 9:39 AM, Jason Lu <jasonlu68@gmail.com> > wrote: > >> >> > >> >> Hi list, > >> >> > >> >> I have a question and would like to get your help. > >> >> What I would like to get is to show the read coverage in the exon > >> >> regions (only) in the ucsc genome browser. My question is how to > >> >> export the Views so I can load into ucsc browser. > >> >> Here is what I have: > >> >> > >> >> # > >> >> >cvg = coverage(ranges(ss)) > >> > > >> > Careful here: you are not distinguishing chromosomes when calculating > >> > this > >> > coverage. It's all going into one vector. Instead, you want to call > >> > coverage > >> > directly on your GRanges 'ss'. > >> > > >> > cvg <- coverage(ss) > >> > > >> >> > >> >> >cvg.view = Views(cvg,rangesexon.gr)) # exon.gr is a GRanges > >> > > >> > Since 'cvg' is now an RleList (with one element per chromosome), you > >> > want a > >> > RangesList to parallel it in your RleViewsList. > >> > > >> > cvg.view <- Views(cvg, asexon.gr, "RangesList")) > >> > > >> > I think we should try to make that easier and have Views() take a > >> > GRanges. > >> > Will make a note. > >> > > >> >> > >> >> >cvg.view > >> >> Views on a 22109556-length Rle subject > >> >> > >> >> views: > >> >> start end width > >> >> [1] 22109317 22109688 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 > 9 9 > >> >> 9 > >> >> ...] > >> >> [2] 22084156 22084276 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 > 4 4 > >> >> 4 > >> >> ...] > >> >> [3] 22083039 22083195 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 > 3 3 > >> >> 4 > >> >> ...] > >> >> [4] 22079485 22079612 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 > 2 2 > >> >> 2 > >> >> ...] > >> >> [5] 22079020 22079144 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 > 6 5 > >> >> 4 > >> >> ...] > >> >> > >> >> I don't know how to modify this view such as adding chromosome info > >> >> and export this 'cvg.view' in rtracklayer. > >> > > >> > > >> > You can now export this RleViewsList directly to a file for upload. > For > >> > upload to the UCSC browser, how about: > >> > > >> > session <- browserSession() > >> > session$coverage <- cvg.view > >> > browserView(session, exon.gr[1]) > >> > > >> > That should show you the first exon. > >> > > >> >> Thanks in advance. > >> >> Jason > >> >> > >> >> > sessionInfo() > >> >> R version 2.14.0 (2011-10-31) > >> >> Platform: x86_64-unknown-linux-gnu (64-bit) > >> >> > >> >> locale: > >> >> [1] C > >> >> > >> >> attached base packages: > >> >> [1] stats graphics grDevices utils datasets methods base > >> >> > >> >> other attached packages: > >> >> [1] rtracklayer_1.14.3 RCurl_1.7-0 bitops_1.0-4.1 > >> >> [4] Rsamtools_1.6.2 Biostrings_2.22.0 > GenomicFeatures_1.6.4 > >> >> [7] AnnotationDbi_1.16.4 Biobase_2.14.0 GenomicRanges_1.6.3 > >> >> [10] IRanges_1.12.2 BiocInstaller_1.2.1 > >> >> > >> >> loaded via a namespace (and not attached): > >> >> [1] BSgenome_1.22.0 DBI_0.2-5 RSQLite_0.10.0 XML_3.4-3 > >> >> [5] biomaRt_2.10.0 tools_2.14.0 zlibbioc_1.0.0 > >> >> > > >> >> > >> >> _______________________________________________ > >> >> Bioconductor mailing list > >> >> Bioconductor@r-project.org > >> >> https://stat.ethz.ch/mailman/listinfo/bioconductor > >> >> Search the archives: > >> >> http://news.gmane.org/gmane.science.biology.informatics.conductor > >> > > >> > > > > > > [[alternative HTML version deleted]]
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Thanks Michael. Hope you have a Happy Thanksgiving! Jason On Wed, Nov 23, 2011 at 4:58 PM, Michael Lawrence <lawrence.michael at="" gene.com=""> wrote: > At this point, > > cvg.select <- subsetByOverlaps(as(cvg, "GRanges"), toshow) > > Should work, but it is not very efficient. We just need a RleViewsList -> > RangedData/GRanges coercion. On the TODO list. > > On Wed, Nov 23, 2011 at 9:35 AM, Jason Lu <jasonlu68 at="" gmail.com=""> wrote: >> >> Hi Michael, >> >> Thanks for the quick response. >> I tried the keepSeqlevels and your solution using the seqselect. It >> works! The only caveat is that the genomic coordinates are lost ?in >> the bedGraph. Here is what I have tried >> >> # >> toshow = keepSeqlevels(toshow,seqlevels(ss)) >> cvg = coverage(ss) >> cvg.select=seqselect(cvg,as(toshow,"RangesList")) >> export(cvg.select,"test.bedGraph") >> >> # output of test.bedGraph [genomic coordinates were lost] >> track name="R Track" type=bedGraph >> chr5 ? ?0 ? ? ? 103 ? ? 0 >> chr5 ? ?103 ? ? 104 ? ? 71 >> chr5 ? ?104 ? ? 105 ? ? 72 >> chr5 ? ?105 ? ? 106 ? ? 74 >> chr5 ? ?106 ? ? 109 ? ? 76 >> chr5 ? ?109 ? ? 110 ? ? 77 >> >> I may need to do shift with each exon start positions, or you may have >> more elegant solutions. >> Thanks. >> >> Jason >> >> >> On Wed, Nov 23, 2011 at 11:38 AM, Michael Lawrence >> <lawrence.michael at="" gene.com=""> wrote: >> > >> > >> > On Wed, Nov 23, 2011 at 7:18 AM, Jason Lu <jasonlu68 at="" gmail.com=""> wrote: >> >> >> >> I want to thank Michael and Martin for being helpful. >> >> >> >> My apology for not showing the full script last email. The purpose >> >> here is to get a figure showing read coverage in the exon regions of >> >> my gene of interest (one gene). I tried some additional steps here and >> >> get an error below. >> >> >> >> # >> >> nm = "NM_000997" >> >> txs ?= exonsBy(txdb,by="tx",use.name=TRUE) >> >> toshow = txs[[nm]] >> >> ss <- >> >> readBamGappedAlignments("myalign.bam",param=ScanBamParam(which=t oshow)) >> >> strand(ss) = "*" >> >> cvg ?= coverage(ss) ?# cvg: SimpleRleList >> >> >> >> cvg.view <- Views(cvg, as(toshow, "RangesList")) >> >> Error in .Method(..., FUN = FUN, MoreArgs = MoreArgs, SIMPLIFY = >> >> SIMPLIFY, >> >> ?: >> >> ?all object lengths must be multiple of longest object length >> >> >> > >> > The problem here is likely that "toshow" is on a wider universe (set of >> > sequences) than your coverage vector from the BAM file. You can use >> > keepSeqlevels(toshow, seqlevels(ss)). You want to make sure the >> > seqlevels >> > are in the same order; not sure if keepSeqlevels() does this -- perhaps >> > it >> > should? >> > >> >> >> >> Also, I have been unsuccessful in exporting the RleViewsList to a file >> >> (wig or bedGraph format). Could you give a hint on this as well? >> >> Thanks again. >> >> >> > >> > Now that I think about it, Views are a bit of an overkill for this >> > specific >> > case. You could just do a >> > >> > cvg.select <- seqselect(cvg, as(toshow, "RangesList")) >> > >> > And then export that: >> > >> > export(cvg.select, "coverage.bedGraph") >> > >> >> Jason >> >> >> >> >> >> On Wed, Nov 23, 2011 at 8:20 AM, Michael Lawrence >> >> <lawrence.michael at="" gene.com=""> wrote: >> >> > >> >> > >> >> > On Tue, Nov 22, 2011 at 9:39 AM, Jason Lu <jasonlu68 at="" gmail.com=""> >> >> > wrote: >> >> >> >> >> >> Hi list, >> >> >> >> >> >> I have a question and would like to get your help. >> >> >> What I would like to get is to show the read coverage in the exon >> >> >> regions (only) in the ucsc genome browser. My question is how to >> >> >> export the Views so I can load into ucsc browser. >> >> >> Here is what I have: >> >> >> >> >> >> # >> >> >> >cvg = coverage(ranges(ss)) >> >> > >> >> > Careful here: you are not distinguishing chromosomes when calculating >> >> > this >> >> > coverage. It's all going into one vector. Instead, you want to call >> >> > coverage >> >> > directly on your GRanges 'ss'. >> >> > >> >> > cvg <- coverage(ss) >> >> > >> >> >> >> >> >> >cvg.view = Views(cvg,rangesexon.gr)) ?# exon.gr is a GRanges >> >> > >> >> > Since 'cvg' is now an RleList (with one element per chromosome), you >> >> > want a >> >> > RangesList to parallel it in your RleViewsList. >> >> > >> >> > cvg.view <- Views(cvg, asexon.gr, "RangesList")) >> >> > >> >> > I think we should try to make that easier and have Views() take a >> >> > GRanges. >> >> > Will make a note. >> >> > >> >> >> >> >> >> >cvg.view >> >> >> Views on a 22109556-length Rle subject >> >> >> >> >> >> views: >> >> >> ? ? ? ?start ? ? ?end width >> >> >> ?[1] 22109317 22109688 ? 372 [5 5 7 5 6 6 6 5 5 5 5 5 4 4 5 8 8 8 9 >> >> >> 9 9 >> >> >> 9 >> >> >> ...] >> >> >> ?[2] 22084156 22084276 ? 121 [4 4 4 3 3 3 3 3 3 3 3 3 3 4 4 4 4 4 4 >> >> >> 4 4 >> >> >> 4 >> >> >> ...] >> >> >> ?[3] 22083039 22083195 ? 157 [2 1 1 0 0 0 1 1 1 1 2 2 2 2 2 2 2 2 2 >> >> >> 3 3 >> >> >> 4 >> >> >> ...] >> >> >> ?[4] 22079485 22079612 ? 128 [0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 2 2 2 >> >> >> 2 2 >> >> >> 2 >> >> >> ...] >> >> >> ?[5] 22079020 22079144 ? 125 [6 6 6 6 7 7 7 7 7 7 7 7 7 7 6 6 6 6 6 >> >> >> 6 5 >> >> >> 4 >> >> >> ...] >> >> >> >> >> >> I don't know how to modify this view such as adding chromosome info >> >> >> and export this 'cvg.view' in rtracklayer. >> >> > >> >> > >> >> > You can now export this RleViewsList directly to a file for upload. >> >> > For >> >> > upload to the UCSC browser, how about: >> >> > >> >> > session <- browserSession() >> >> > session$coverage <- cvg.view >> >> > browserView(session, exon.gr[1]) >> >> > >> >> > That should show you the first exon. >> >> > >> >> >> Thanks in advance. >> >> >> Jason >> >> >> >> >> >> > sessionInfo() >> >> >> R version 2.14.0 (2011-10-31) >> >> >> Platform: x86_64-unknown-linux-gnu (64-bit) >> >> >> >> >> >> locale: >> >> >> [1] C >> >> >> >> >> >> attached base packages: >> >> >> [1] stats ? ? graphics ?grDevices utils ? ? datasets ?methods ? base >> >> >> >> >> >> other attached packages: >> >> >> ?[1] rtracklayer_1.14.3 ? ?RCurl_1.7-0 ? ? ? ? ? bitops_1.0-4.1 >> >> >> ?[4] Rsamtools_1.6.2 ? ? ? Biostrings_2.22.0 >> >> >> GenomicFeatures_1.6.4 >> >> >> ?[7] AnnotationDbi_1.16.4 ?Biobase_2.14.0 ? ? ? ?GenomicRanges_1.6.3 >> >> >> [10] IRanges_1.12.2 ? ? ? ?BiocInstaller_1.2.1 >> >> >> >> >> >> loaded via a namespace (and not attached): >> >> >> [1] BSgenome_1.22.0 DBI_0.2-5 ? ? ? RSQLite_0.10.0 ?XML_3.4-3 >> >> >> [5] biomaRt_2.10.0 ?tools_2.14.0 ? ?zlibbioc_1.0.0 >> >> >> > >> >> >> >> >> >> _______________________________________________ >> >> >> Bioconductor mailing list >> >> >> Bioconductor at r-project.org >> >> >> https://stat.ethz.ch/mailman/listinfo/bioconductor >> >> >> Search the archives: >> >> >> http://news.gmane.org/gmane.science.biology.informatics.conductor >> >> > >> >> > >> > >> > > >
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