This repository was archived by the owner on Aug 6, 2021. It is now read-only.
-
Notifications
You must be signed in to change notification settings - Fork 6
Barcode Discovery
Koen Herten edited this page Feb 26, 2014
·
2 revisions
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:
-
-f1
the name of the input file (mandatory)
Optional parameters: -
-min
the minimum length of the barcode (standard 6) -
-max
the maximum length of the barcode (standard 10) -
-gzip
use gzip files as input and output (standard false) -
-o
the output directory (standard the directory of execution) -
-ea
Add 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) -
-er
Replace 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) -
-barmin
The minimum occurance of a barcode before it is shown in the results (standard: 200) -
-barmax
The maximum occurance of barcodes shown in the output (increasing this number will increase ram usage, but gives a slightly better result) (standard: 100) -
-barmis
The percentage of mismatches that may occure between barcodes (integer between 1 and 10) (standard: 10)