tag2peak Code
Extract significant peaks from CLIP tags using scan statistics
Brought to you by:
zhangchaolin
File | Date | Author | Commit |
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README | 2013-02-21 |
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[10e54e] Initial release to the public |
bedUniq.pl | 2013-02-21 |
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[10e54e] Initial release to the public |
combineTranscripts.pl | 2013-02-21 |
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[10e54e] Initial release to the public |
gene2ExonIntron.pl | 2013-02-21 |
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[10e54e] Initial release to the public |
tag2peak.pl | 2013-02-21 |
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[10e54e] Initial release to the public |
tag2profile.pl | 2013-02-21 |
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[10e54e] Initial release to the public |
tagoverlap.pl | 2013-02-21 |
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[10e54e] Initial release to the public |
A typical command line: perl ~/path/to/dir/tag2peak.pl -ss --multi-test -v gene.in.bed tag.in.bed peak.out.bed gene.in.bed is the gene annotation file. tag.in.bed is the CLIP tag file. If you do not want to distinguish exons and introns, provide a gene.in.bed file with the first 6 columns. Otherwise, provide a 12-column BED file with additional information of exon/intron structure. If your tag.in.bed file is large (e.g., > 6M tags), run with an additional option -big If you want to normalize by gene expression level, provide the abundance (linear scale) in the score (5th) column gene.in.bed file.