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  "Type": "Package",
  "Title": "An R package to automate the analysis of double-strand break\nrepair during meiosis",
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  "Authors@R": "c(person(given = \"Lucy\",\nfamily = \"McNeill\",\nrole = c(\"aut\", \"cre\", \"cph\"),\nemail = \"luc.mcneill@gmail.com\",\ncomment = c(ORCID = \"0000-0003-1752-4882\")),\nperson(given = \"Wayne\",\nfamily = \"Crismani\",\nrole = c(\"rev\", \"ctb\"),\ncomment = c(ORCID = \"0000-0003-0143-8293\")))",
  "Description": "Synapsis is a Bioconductor software package for automated\n(unbiased and reproducible) analysis of meiotic\nimmunofluorescence datasets. The primary functions of the\nsoftware can i) identify cells in meiotic prophase that are\nlabelled by a synaptonemal complex axis or central element\nprotein, ii) isolate individual synaptonemal complexes and\nmeasure their physical length, iii) quantify foci and\nco-localise them with synaptonemal complexes, iv) measure\ninterference between synaptonemal complex-associated foci. The\nsoftware has applications that extend to multiple species and\nto the analysis of other proteins that label meiotic prophase\nchromosomes. The software converts meiotic immunofluorescence\nimages into R data frames that are compatible with machine\nlearning methods. Given a set of microscopy images of meiotic\nspread slides, synapsis crops images around individual single\ncells, counts colocalising foci on strands on a per cell basis,\nand measures the distance between foci on any given strand.",
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  "License": "MIT + file LICENSE",
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  "Repository": "https://bioc.r-universe.dev",
  "Date/Publication": "2026-04-28 12:57:20 UTC",
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    "User": "root"
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