ExomeCopy package error
0
0
Entering edit mode
Guest User ★ 13k
@guest-user-4897
Last seen 10.2 years ago
Hi, I am testing ExomeCopy on a set of illumina sequencing data generated after agilent custum gene set capture, only 35 gene exons overall (~ 300 Mb total). 1-My first question would be : is the method reliable for smaller capture? 2-Secondly., I sucessfully used the method on the data provided with the vignette. I then tried with my own set of data in total 10 samples, across 2282 rows , I have calculated the GC and bg values nad went on to the next step where I ran exomeCopy on one sample and one chromosome ###this seems to work for certains samples, expect the warning for small subset > fit <- exomeCopy(rdata["Chr10"], sample.name = exome.samples[10], + X.names = c("bg", "GC", "GC.sq", "width"), S = 0:6, + d = 2) Warning message: In exomeCopy(rdata["Chr10"], sample.name = exome.samples[10], X.names = c("bg", : exomeCopy was tested for thousands of ranges covering a targeted region on a single chromosome. The results might not be reliable for less than a hundred ranges. ###then I try with another sample and got this error message Error in if (goto.cnv < 1/(nstates - 1)) { : missing value where TRUE/FALSE needed I am not sure where this comes from and would like some help on this > fit <- exomeCopy(rdata["Chr10"], sample.name = exome.samples[7], + X.names = c("bg", "GC", "GC.sq", "width"), S = 0:6, + d = 2) Error in if (goto.cnv < 1/(nstates - 1)) { : missing value where TRUE/FALSE needed In addition: Warning message: In exomeCopy(rdata["Chr10"], sample.name = exome.samples[7], X.names = c("bg", : exomeCopy was tested for thousands of ranges covering a targeted region on a single chromosome. The results might not be reliable for less than a hundred ranges. > exome.samples [1] "sample9" "sample8" "sample7" "sample6" "sample5" "sample1" [7] "sample16" "sample15" "sample14" "sample13" example if my data ##### RangedData with 2282 rows and 15 value columns across 18 spaces space ranges | sample9 sample8 sample7 <factor> <iranges> | <integer> <integer> <integer> 1 Chr1 [115247069, 115247168] | 4369 4446 3675 2 Chr1 [115247169, 115247268] | 8222 8081 6978 3 Chr1 [115247269, 115247368] | 9548 10026 8690 -- output of sessionInfo(): R version 2.15.0 (2012-03-30) Platform: x86_64-unknown-linux-gnu (64-bit) locale: [1] LC_CTYPE=en_GB.UTF-8 LC_NUMERIC=C [3] LC_TIME=en_GB.UTF-8 LC_COLLATE=en_GB.UTF-8 [5] LC_MONETARY=en_GB.UTF-8 LC_MESSAGES=C [7] LC_PAPER=C LC_NAME=C [9] LC_ADDRESS=C LC_TELEPHONE=C [11] LC_MEASUREMENT=en_GB.UTF-8 LC_IDENTIFICATION=C attached base packages: [1] stats graphics grDevices utils datasets methods base other attached packages: [1] exomeCopy_1.2.0 Rsamtools_1.8.6 Biostrings_2.24.1 [4] GenomicRanges_1.8.13 IRanges_1.14.4 BiocGenerics_0.2.0 loaded via a namespace (and not attached): [1] bitops_1.0-4.1 stats4_2.15.0 tools_2.15.0 zlibbioc_1.2.0 -- Sent via the guest posting facility at bioconductor.org.
Sequencing exomeCopy Sequencing exomeCopy • 1.2k views
ADD COMMENT

Login before adding your answer.

Traffic: 639 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