generate_complement

Generate the complementary sequence of a nucleic acid sequence, with an option to reverse it.

Accurate calculation of nucleic acid melting temperature (Tm) is fundamental to many molecular biology applications, and this software scales Tm analysis from individual sequences to genome‑wide thermodynamic profiling. This package extends Tm analysis from simple sequence level computation to comprehensive genome-wide thermodynamic profiling. It takes multiple input formats including sequence strings, FASTA files, genomic coordinates. The implementation provides three Tm calculation methods: the Wallace rule (Thein & Wallace, 1986), empirical GC‑content formulas (Marmur, 1962; Schildkraut, 2010; Wetmur, 1991; Untergasser, 2012; von Ahsen, 2001), and nearest‑neighbor thermodynamics (Breslauer, 1986; Sugimoto, 1996; Allawi, 1998; SantaLucia, 2004; Freier, 1986; Xia, 1998; Chen, 2012; Bommarito, 2000; Turner, 2010; Sugimoto, 1995; Allawi, 1997; SantaLucia, 2005). Twenty-seven nearest-neighbor parameter sets are provided, covering DNA, RNA and RNA/DNA hybrid duplexes. These include sets obtained by melting-temperature optimization that are fitted directly at a stated sodium concentration (Weber, 2015; Ferreira, 2019; Basilio Barbosa, 2019), which replace salt correction rather than being corrected; salt correction is skipped automatically when the requested condition matches the one a set was fitted at. Corrections are otherwise supported for salt ions (SantaLucia, 1996, 1998; Owczarzy, 2004, 2008) and for chemical conditions such as dimethyl sulfoxide and formamide. This package returns result as a GRanges object for interoperability with Bioconductor workflows and downstream multi-omics analyses. Data-level integration reconciles Tm windows with external multi-omics GRanges objects through overlap, nearest-feature, windowed-count, and binned-average strategies, returning a single unified GRanges object ready for downstream analysis. Visualization-level integration renders multiple feature layers as independent concentric tracks on a shared genomic axis, each retaining its native coordinate resolution. Group comparison supports Wilcoxon rank-sum and Student's t-tests with multiple available correction methods for contrasting Tm and other features across region classes.

Junhui Li

TmCalculator

Genome-Wide Nucleic Acid Melting Temperature Profiling and
Multi-Omics Integration

Lihua Julie Zhu

generate_complement function

<dl><dt>input_seq</dt>
<dd>Input sequence(s) in 5' to 3' direction. Must be provided as either:
- A character string (e.g., c("ATGCG", "GCTAG"))</dd>
<dt>reverse</dt>
<dd>Logical. If TRUE, the complementary sequence is reversed (3' to 5').
If FALSE (default), the complementary sequence is in the same direction (5' to 3').</dd></dl>

Arguments

Author

Generate complementary sequence — generate_complement

<dl>

<dt>input_seq</dt>
<dd>Input sequence(s) in 5' to 3' direction. Must be provided as either:
- A character string (e.g., c("ATGCG", "GCTAG"))</dd>


<dt>reverse</dt>
<dd>Logical. If TRUE, the complementary sequence is reversed (3' to 5').
If FALSE (default), the complementary sequence is in the same direction (5' to 3').</dd>

</dl>

generate_complement: Generate complementary sequence

Description

Usage

Value

Arguments

Author

References

Examples