Originally posted by zhengz
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So when I try these commands, I get ERROR: Default MID sets gsMIDs and flMIDs do not exist in configuration file. What is odd is that they do. I don't even want to use the MIDConfig.Parse file which is why I use the -mcf command so I think it is very odd. Should I put my barcode.txt file in the config folder?
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With -s you tell sfffile to split default barcodes from default barcode file.Originally posted by aligenie View PostSo when I try these commands, I get ERROR: Default MID sets gsMIDs and flMIDs do not exist in configuration file. What is odd is that they do. I don't even want to use the MIDConfig.Parse file which is why I use the -mcf command so I think it is very odd. Should I put my barcode.txt file in the config folder?
Put your barcodes as supposed into a file, and then, in your case use e.g.
sfffile -s barcode -o myNewSFF -mcf /path/to/barcodefile *.sff
cheers,
Sven
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For some reason, that still doesn't work. Oh well, thanks for your help. Maybe I'll figure something out eventually. This is a bit of a mystery to me!Originally posted by sklages View PostWith -s you tell sfffile to split default barcodes from default barcode file.
Put your barcodes as supposed into a file, and then, in your case use e.g.
sfffile -s barcode -o myNewSFF -mcf /path/to/barcodefile *.sff
cheers,
Sven
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Hi ali,
I guess the sfffile looks for the barcode set which you define in your barcode file and the name you specify in the command line after -s. If no match, it continues to look for gsMID and rlMID. Maybe you can remove the lines after gsMID or rlMID (yes, save a copy first), and see what the error message suggests you. Hope it works out for you eventually.
A side note: I think it is better to avoid using "*.sff", which will combine the samples having the same barcode but from different physically separated Regions (Lanes) in one sff file. Better to spell out the sff file name, instead of using wildcard. But if you have no sent the results to others, no worries, you will notice the problem, and it is quick to run the sfffile command again. It finishes in a minute.Last edited by zhengz; 04-22-2011, 11:59 PM.
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
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