Closed bfrommer closed 2 years ago
This looks somewhat familiar but I don't remember exactly what the issue was. Can you send your sessionInfo()
output?
Also, if you just type first
in the command line, which namespace does first
belong to?
Here is my sessionInfo() output:
R version 4.1.1 (2021-08-10)
Platform: x86_64-conda-linux-gnu (64-bit)
Running under: Ubuntu 20.04.3 LTS
Matrix products: default
BLAS/LAPACK: /prj/gf-biotools/programs/miniconda3/envs/r_topGo/lib/libopenblasp-r0.3.17.so
locale:
[1] LC_CTYPE=de_DE.UTF-8 LC_NUMERIC=C LC_TIME=de_DE.UTF-8 LC_COLLATE=de_DE.UTF-8
[5] LC_MONETARY=de_DE.UTF-8 LC_MESSAGES=de_DE.UTF-8 LC_PAPER=de_DE.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C LC_MEASUREMENT=de_DE.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] parallel stats4 stats graphics grDevices utils datasets methods base
other attached packages:
[1] rtracklayer_1.52.1 GenomicRanges_1.44.0 GenomeInfoDb_1.28.4 IRanges_2.26.0 S4Vectors_0.30.2
[6] BiocGenerics_0.38.0 gggenomes_0.9.4.9000 snakecase_0.11.0 jsonlite_1.7.2 tibble_3.1.5
[11] thacklr_0.0.0.9000 tidyr_1.1.4 stringr_1.4.0 readr_2.0.2 purrr_0.3.4
[16] gggenes_0.4.1 ggplot2_3.3.5 dplyr_1.0.7
loaded via a namespace (and not attached):
[1] matrixStats_0.61.0 bitops_1.0-7 fs_1.5.0 usethis_2.1.3
[5] devtools_2.4.2 bit64_4.0.5 RColorBrewer_1.1-2 rprojroot_2.0.2
[9] tools_4.1.1 utf8_1.2.2 R6_2.5.1 DBI_1.1.1
[13] colorspace_2.0-2 withr_2.4.2 tidyselect_1.1.1 prettyunits_1.1.1
[17] processx_3.5.2 bit_4.0.4 curl_4.3.2 compiler_4.1.1
[21] git2r_0.28.0 Biobase_2.52.0 cli_3.1.0 DelayedArray_0.18.0
[25] desc_1.4.0 labeling_0.4.2 scales_1.1.1 callr_3.7.0
[29] digest_0.6.28 Rsamtools_2.8.0 XVector_0.32.0 pkgconfig_2.0.3
[33] sessioninfo_1.2.1 MatrixGenerics_1.4.3 fastmap_1.1.0 rlang_0.4.12
[37] rstudioapi_0.13 BiocIO_1.2.0 farver_2.1.0 generics_0.1.1
[41] BiocParallel_1.26.2 vroom_1.5.5 RCurl_1.98-1.5 magrittr_2.0.1
[45] GenomeInfoDbData_1.2.6 Matrix_1.3-4 munsell_0.5.0 fansi_0.5.0
[49] ggfittext_0.9.1 lifecycle_1.0.1 stringi_1.7.5 yaml_2.2.1
[53] SummarizedExperiment_1.22.0 zlibbioc_1.38.0 pkgbuild_1.2.0 grid_4.1.1
[57] crayon_1.4.2 lattice_0.20-45 Biostrings_2.60.2 hms_1.1.1
[61] ps_1.6.0 pillar_1.6.4 rjson_0.2.20 pkgload_1.2.3
[65] XML_3.99-0.8 glue_1.4.2 remotes_2.4.1 BiocManager_1.30.16
[69] vctrs_0.3.8 tzdb_0.2.0 testthat_3.1.0 gtable_0.3.0
[73] assertthat_0.2.1 cachem_1.0.6 restfulr_0.0.13 GenomicAlignments_1.28.0
[77] memoise_2.0.0 ellipsis_0.3.2
When typing in first, this is my first line:
standardGeneric for "first" defined from package "S4Vectors"
Ah, ok. Try first <- dplyr::first
just before reading the gff as a workaround. I think that should do the trick.
If that works I will fix read_gff
to explicitly to dplyr::first
in the next release.
Yes, now this error is gone! But it gives me an other error?
> first <- dplyr::first
> g0 <- read_feats(ex("emales/emales.gff"))
Reading 'gff3' with `read_gff3()`:
* file_id: emales [/.../gggenomes/extdata/emales/emales.gff]
Harmonizing attribute names
* ID -> feat_id
* Name -> name
* Note -> note
Error in rename(mrna_introns, mrna_introns.. = introns) :
Object 'introns' not found
OK, seems related to the same namespace collision. Can you restart R and load S4Vectors first?
library(S4Vectors)
library(gggenomes)
read_feats(ex("emales/emales.gff"))
Thanks! It works just fine.
Great!
I'm reopening and renaming this issue until I fixed it in the package
Hello,
I have problems with loading my own gff3 files and also the emales example gff files. When I execute
I get
The same happens also with directly using read_gff3(). I hope you can help me. Thanks!