[Bioc-devel] proposal for additional seqlevelsStyle
hi Herv?, i didn't know about this new sequence style until Vince posted his message and we briefly talked about it at the European BioC meeting this week in Brussels. however, i didn't know that the style was specific to a particular assembly. i have no use case of this at the mome moment, i.e., i have not encountered myself any annotation or BAM file with chromosome names written that way, so i don't know how pressing this issue is, maybe Vince can tell us how spread such chromosome naming style may become in the near future. naively, i'd think that it would be matter of adding a reference-specific column, i.e., 'GRCh38.p13', 'GRCh37.p13', etc., but i can imagine that maybe the "reference style" concept might not be the appropriate placeholder to map all different chromosome names of all different individual human genomes uploaded to NCBI. maybe we should wait until we have a specific use case .. Vince? robert.
On 12/11/19 10:06 PM, Pages, Herve wrote:
Hi Vince, Robert, Looks like Vince wants the RefSeq accession e.g. NC_000017.11 for chrom 17 in the GRCh38. @Robert: Is this what you're also interested in? The problem is that the RefSeq accessions are specific to a particular assembly (e.g. NC_000017.11 for chrom 17 in GRCh38 but NC_000017.10 for the same chrom in GRCh37). Currently seqlevelsStyle() doesn't know how to distinguish between different assemblies of the same organism. Not saying it couldn't but it would require some thinking and some significant refactoring. It wouldn't be just a matter of adding a column to genomeStyles()$Homo_sapiens. H. On 12/10/19 14:19, Robert Castelo wrote:
I second this, and would suggest to name the style as 'GRC' for "Genome Reference Consortium". thanks Vince for bringing this up, being able to easily switch between genome styles is great. if 'paste0()' in R is one of the most influential contributions to statistical computing https://urldefense.proofpoint.com/v2/url?u=https-3A__simplystatistics.org_2013_01_31_paste0-2Dis-2Dstatistical-2Dcomputings-2Dmost-2Dinfluential-2Dcontribution-2Dof-2Dthe-2D21st-2Dcentury&d=DwICAg&c=eRAMFD45gAfqt84VtBcfhQ&r=BK7q3XeAvimeWdGbWY_wJYbW0WYiZvSXAJJKaaPhzWA&m=LCcYSINIz3XXhf8i-26IegXRLkTO1NgVbvzgvnPA3dc&s=b0_SIu8orJ7ZcCS3TIodFvGTPibt9R8vFL5Y40YSx3Q&e= i think that 'seqlevelsStyle()' from the GenomeInfoDb package is one of the most influential contributions to human genetics, if you think about the time invested by researchers in parsing and changing between different styles of chromosome names :) robert. On 06/12/2019 15:03, Vincent Carey wrote:
I raised this issue previously with little response. I'd propose that we add a column or two to genomeStyles()$Homo_sapiens
head(genomeStyles()$Homo_sapiens, 2)
?? circular auto?? sex NCBI UCSC dbSNP Ensembl 1??? FALSE TRUE FALSE??? 1 chr1?? ch1?????? 1 2??? FALSE TRUE FALSE??? 2 chr2?? ch2?????? 2 that includes the values for "NCBI reference sequence names" See https://urldefense.proofpoint.com/v2/url?u=https-3A__www.ncbi.nlm.nih.gov_nuccore_568815581&d=DwICAg&c=eRAMFD45gAfqt84VtBcfhQ&r=BK7q3XeAvimeWdGbWY_wJYbW0WYiZvSXAJJKaaPhzWA&m=LCcYSINIz3XXhf8i-26IegXRLkTO1NgVbvzgvnPA3dc&s=3Jy-MH7heIcrc_A4qm_izduLvBoPWHSeq4gdxf5nv24&e= for one report on chr17, and https://urldefense.proofpoint.com/v2/url?u=https-3A__www.ncbi.nlm.nih.gov_assembly_GCF-5F000001405.39&d=DwICAg&c=eRAMFD45gAfqt84VtBcfhQ&r=BK7q3XeAvimeWdGbWY_wJYbW0WYiZvSXAJJKaaPhzWA&m=LCcYSINIz3XXhf8i-26IegXRLkTO1NgVbvzgvnPA3dc&s=y6ut_Xcc4rSbXanckiJhiwLsL0W8neJfKWQa6wnG3aM&e= for a table that includes the Genbank labels. Should I just file a PR at https://urldefense.proofpoint.com/v2/url?u=https-3A__github.com_Bioconductor_GenomeInfoDb_&d=DwICAg&c=eRAMFD45gAfqt84VtBcfhQ&r=BK7q3XeAvimeWdGbWY_wJYbW0WYiZvSXAJJKaaPhzWA&m=LCcYSINIz3XXhf8i-26IegXRLkTO1NgVbvzgvnPA3dc&s=KMzfo3_8kkJ-wdvRCNP5rUjTVMW87brj07yHaKL5Qb0&e= after testing?
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Robert Castelo, PhD Associate Professor Dept. of Experimental and Health Sciences Universitat Pompeu Fabra (UPF) Barcelona Biomedical Research Park (PRBB) Dr Aiguader 88 E-08003 Barcelona, Spain telf: +34.933.160.514 fax: +34.933.160.550