Tag: KaryoploteR
Bioconductor – karyoploteR
DOI: 10.18129/B9.bioc.karyoploteR This package is for version 3.13 of Bioconductor; for the stable, up-to-date release version, see karyoploteR. Plot customizable linear genomes displaying arbitrary data Bioconductor version: 3.13 karyoploteR creates karyotype plots of arbitrary genomes and offers a complete set of functions to plot arbitrary data on them….
Two transects reveal remarkable variation in gene flow on opposite ends of a European toad hybrid zone
Abbott R, Albach D, Ansell S, Arntzen JW, Baird SJE, Bierne N, Zinner D (2013) Hybridization and speciation. J Evolut Biol 26:229–246. doi.org/10.1111/j.1420-9101.2012.02599.x Article CAS Google Scholar Arntzen JW (2019) An amphibian species pushed out of Britain by a moving hybrid zone. Mol Ecol 28:5145–5154 Article PubMed PubMed Central Google…
Newly identified sex chromosomes in the Sphagnum (peat moss) genome alter carbon sequestration and ecosystem dynamics
Yu, Z., Loisel, J., Brosseau, D. P., Beilman, D. W. & Hunt, S. J. Global peatland dynamics since the Last Glacial Maximum. Geophys. Res. Lett. 37, L13402 (2010). van Breemen, N. How Sphagnum bogs down other plants. Trends Ecol. Evol. 10, 270–275 (1995). Article Google Scholar Johnson, M. G. et…
A chromosome-level genome assembly of Plantago ovata
Genome assembly and chromosome identification A Plantago ovata genome reference was generated by utilizing a total of 5.98 M (7 cells, 40.21 Gb, N50 = 10.45 Kb, 50 bp–121.17 Kb) PacBio long reads and 636.5 million (47.74 Gb) Hi-C short-reads. PacBio reads were used to assemble contigs, while Hi-C reads were used to achieve chromosome-level assembly. The final…
karyoploteR: uncircle your genomes
Hi all, I’d like to present karyoploteR, an R/Bioconductor package we have developed to plot any data on any genome in non-circular layouts. The goal of this project was to develop a tool as flexible as Circos, but easier to use and representing genomes as straight lines instead of circles,…
Color label of rainfall plot drawn by KaryoploteR
You can use the standard legend() command as outlined in this issue here: support.bioconductor.org/p/124328/ Minimal example based on bernatgel.github.io/karyoploter_tutorial//Examples/Rainfall/Rainfall.html : library(karyoploteR) somatic.mutations <- read.table(file=”ftp://ftp.sanger.ac.uk/pub/cancer/AlexandrovEtAl/somatic_mutation_data/Pancreas/Pancreas_raw_mutations_data.txt”, header=FALSE, sep=”t”, stringsAsFactors=FALSE) somatic.mutations <- setNames(somatic.mutations, c(“sample”, “mut.type”, “chr”, “start”, “end”, “ref”, “alt”, “origin”)) somatic.mutations <- split(somatic.mutations, somatic.mutations$sample) sm <- somatic.mutations[[“APGI_1992”]] sm.gr <- toGRanges(sm[,c(“chr”, “start”, “end”,…