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Barcode Discovery
Koen Herten edited this page Feb 26, 2014
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This program searches for possible barcodes and barcode enzyme combinations.
Designed for the discovery of sequencing errors, or unused barcodes when a large
proportion of the demultiplex is undetermined.
Mandatory parameters:
-
-f1the name of the input file (mandatory)
Optional parameters: -
-minthe minimum length of the barcode (standard 6) -
-maxthe maximum length of the barcode (standard 10) -
-gzipuse gzip files as input and output (standard false) -
-othe output directory (standard the directory of execution) -
-eaAdd enzymes from the given file (keeps the standard enzymes, and add the new) (enzyme file: no header, enzyme name tab cutsites (multiple cutsites are comma separeted)) (example: enzyme ApeKI and restriction site G^CWGC: "ApeKI \tab CAGC,CTGC") (only use once, not use -er) -
-erReplace enzymes from the given file (do not keep the standard enzymes) (enzyme file: no header, enzyme name tab cutsites (multiple cutsites are comma separeted)) (example: enzyme ApeKI and restriction site G^CWGC: "ApeKI \tab CAGC,CTGC") (only use once, not use -ea) -
-barminThe minimum occurance of a barcode before it is shown in the results (standard: 200) -
-barmaxThe maximum occurance of barcodes shown in the output (increasing this number will increase ram usage, but gives a slightly better result) (standard: 100) -
-barmisThe percentage of mismatches that may occure between barcodes (integer between 1 and 10) (standard: 10)