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The BASH scripts were used in bioinformatical analysis of next-generation sequencing data from DNase I digested genomes.
Aggregated_Plot: Distinct binding profile of transcription factors was visualized while aggregated DNase I cleavage was plotted to distance from motif centers.
Cleavage_Heatmap: Distinct binding profile of transcription factors was visualized while DNase I cleavage was plotted to distance from motif centers on heatmap.
Conservation_Plot: Sequence conservation of motif instances was plotted to distance from motif centers.
Cut_Counts_and_Density: Frequency of DNase I cleavage was calculated as counts of sequencing tags at each nucleotide, and density file of DNase I cleavage was generated across the genome.
DESeq: Sequencing data of multiple microbial cultures were compared with the R package "DESeq" to test for differential sensitivity to DNase I cleavage.
FIMO: Genome was scanned with FIMO (Find Individual Motif Occurences) of the MEME Suite to locate potential motif instances of the known transcription factors.
Footprints_Location: Footprints were summarized according to their relative distances from the nearest transcription start sites, gene start sites, or sigma factor binding sites.
Fragment_VPlot: Distinct binding profile of transcription factors was visualized as V-shape gaps while lengths of paired-end sequencing fragments were plotted to distance from motif centers.
Genome_Alignment: Sequencing reads were aligned to unique positions on microbial genome with Burrows-Wheeler Aligner.
MEME: Motifs of transcription factors were detected with MEME (Multiple Em for Motif Elicitation) of the MEME Suite, the motif-based sequence analysis tools.
SPP: DNase I hypersensitive sites were located with the R package "SPP" as regions condensed with sequencing tags.