Mercurial > repos > rnateam > bctools
comparison merge_pcr_duplicates.xml @ 6:1bfc5a5de843 draft
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author | rnateam |
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date | Wed, 04 Nov 2015 07:18:06 -0500 |
parents | bf5b606f1aa7 |
children | 17ef0e0dae68 |
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5:e841de88235c | 6:1bfc5a5de843 |
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1 <tool id="merge_pcr_duplicates.py" name="merge_pcr_duplicates.py" version="0.1.0"> | 1 <tool id="merge_pcr_duplicates.py" name="Merge PCR duplicates" version="0.1.0"> |
2 <description>Merge PCR duplicates according to random barcode library.</description> | 2 <description>according to random barcode library.</description> |
3 <macros> | 3 <macros> |
4 <import>macros.xml</import> | 4 <import>macros.xml</import> |
5 </macros> | 5 </macros> |
6 <expand macro="requirements" /> | 6 <expand macro="requirements" /> |
7 <expand macro="stdio" /> | 7 <expand macro="stdio" /> |
33 <help><![CDATA[ | 33 <help><![CDATA[ |
34 Merge PCR duplicates according to random barcode library. | 34 Merge PCR duplicates according to random barcode library. |
35 | 35 |
36 Barcodes containing uncalled base 'N' are removed. | 36 Barcodes containing uncalled base 'N' are removed. |
37 | 37 |
38 Input: | 38 Input:: |
39 | |
39 * bed6 file containing alignments with fastq read-id in name field | 40 * bed6 file containing alignments with fastq read-id in name field |
40 * fasta library with fastq read-id as sequence ids | 41 * fasta library with fastq read-id as sequence ids |
41 | 42 |
42 Output: | 43 Output:: |
44 | |
43 * bed6 file with random barcode in name field and number of PCR duplicates as score, sorted by fields chrom, start, stop, strand, name | 45 * bed6 file with random barcode in name field and number of PCR duplicates as score, sorted by fields chrom, start, stop, strand, name |
44 | 46 |
45 Author: Daniel Maticzka | 47 Author: Daniel Maticzka |
46 Copyright: 2015 | 48 Copyright: 2015 |
47 License: Apache | 49 License: Apache |