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It enables\nusers to import SNP count data from variant files, perform\nallele-specific read count extraction, and statistically detect\nSNPs showing significant differences in allele expression\nbetween biological conditions or sample groups. This package\ncontains tools for calculating SNP-index and Delta SNP-index\nfrom VCF-derived allele depth data with statistical testing and\nfiltering, including sliding-window analysis of genomic\nregions.", "License": "GPL-3", "Encoding": "UTF-8", "NeedsCompilation": "no", "Packaged": { "Date": "2026-05-19 05:49:38 UTC", "User": "root" }, "RoxygenNote": "7.3.3", "Author": "Sayanti Guha Majumdar [aut, cre], Saima Bano [aut], Nandita\nBanerjee [aut], Rahul Kumar Tiwari [aut], Dipro Sinha [aut],\nSubham Ghosh [aut], Sanjeev Kumar [aut]", "Repository": "https://cran.r-universe.dev", "Date/Publication": "2026-03-19 15:00:22 UTC", "RemoteUrl": "https://github.com/cran/DESNP", "RemoteRef": "HEAD", "RemoteSha": "056b8fae83e010176fe9d2de47bd18e9c1cb88ca", "MD5sum": "91411963bc92a350fc76dcbc7bf8f678", "_user": "cran", "_type": "src", "_file": "DESNP_0.1.0.tar.gz", "_fileid": "54174b6946b702cda49a1d47c7f491ed4bed643b627f6b0c9303cff58e51bb19", "_filesize": 197460, "_sha256": 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