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seq2R

Simple Method to Detect Compositional Changes in Genomic Sequences

This software is useful for loading '.fasta' or '.gbk' files, and for retrieving sequences from 'GenBank' dataset <https://www.ncbi.nlm.nih.gov/genbank/>. This package allows to detect differences or asymmetries based on nucleotide composition by using local linear kernel smoothers. Also, it is possible to draw inference about critical points (i. e. maximum or minimum points) related with the derivative curves. Additionally, bootstrap methods have been used for estimating confidence intervals and speed computational techniques (binning techniques) have been implemented in 'seq2R'.

Versions across snapshots

VersionRepositoryFileSize
2.0.1 rolling linux/jammy R-4.5 seq2R_2.0.1.tar.gz 92.4 KiB
2.0.1 rolling linux/noble R-4.5 seq2R_2.0.1.tar.gz 93.3 KiB
2.0.1 rolling source/ R- seq2R_2.0.1.tar.gz 36.1 KiB
2.0.1 latest linux/jammy R-4.5 seq2R_2.0.1.tar.gz 92.4 KiB
2.0.1 latest linux/noble R-4.5 seq2R_2.0.1.tar.gz 93.3 KiB
2.0.1 latest source/ R- seq2R_2.0.1.tar.gz 36.1 KiB
2.0.1 2026-04-26 source/ R- seq2R_2.0.1.tar.gz 36.1 KiB
2.0.1 2026-04-23 source/ R- seq2R_2.0.1.tar.gz 36.1 KiB
2.0.1 2026-04-09 windows/windows R-4.5 seq2R_2.0.1.zip 268.5 KiB
2.0.1 2025-04-20 source/ R- seq2R_2.0.1.tar.gz 36.1 KiB

Dependencies (latest)

Imports