Nadia Davidson
Nadia Davidson
Hi, I would like to use clustering that's come from another source, and just use RATTLE for the error correction and polishing. Is this possible? If so, what format and...
index_complete.txt can't be found (but is placed in the working directory). replace exec "touch index_complete.txt" with exec "touch $output.dir/index_complete.txt" in clinker.pipe ?
> source("https://bioconductor.org/biocLite.R") Error: With R version 3.5 or greater, install Bioconductor packages using BiocManager; see https://bioconductor.org/install Hope the above makes sense.
See https://groups.google.com/forum/#!topic/corset-project/lCRQT0lUfgA
Many false positives seem to be a result of poor alignment of contigs to the genome, which are resulting is bad annoation. e.g. k49_1134199 0 chr21 44220603 3 281S16M6810N5M2435N6M6199N13M50029N16M1I6M32I32M21I4M4911N3M16052N8M8047N10M2202N2I11M1I25M3I22M6D11M750N10M1163N4M1809N3M1264N7M24156N4M6825N5M3920N2M12899N7M4539N3M7819N8M10199N7M1D1M4453N8M5667N2M11730N3M55386N4M402730N2M6445N3I6M15389N1M13514N9M1I47M2N4I126M15D1279M *...
In the stage that aligns superTranscriptome against each other.
-p assemblyFasta= in params.txt being interpreted with non-empty value. Makes the pipeline assume that an assembly has been provided. Tried setting to '',"","\'\'" etc. but that wasn't interpreted correctly by...