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I have a large sequencing library that I needed to split into 10 smaller files so I could run FastK on different nodes. Following the instructions in the README, I ran FastK on the split files with the following command:
I noticed that there are no k-mers with a count lower than 4 in the merged library histogram. I repeated the process a few times, combining different files, and the merged histograms consistently lack smaller k-mer counts (i.e., they start at 4 or 5). I’m unsure if this behavior is expected, as I do not understand why there are no single-occurrence k-mers. Is this a bug, or am I misunderstanding or misusing the tool?
Thanks for your assistance!
The text was updated successfully, but these errors were encountered:
Dear Gene,
I have a large sequencing library that I needed to split into 10 smaller files so I could run
FastK
on different nodes. Following the instructions in the README, I ranFastK
on the split files with the following command:This produced a
*.hist
and a*.ktab
file for each*.split.fastq
file. I looked at the k-mer count histogram for each split file:Histex -G library_split_01.hist > library_split_01.histogram
I then merged the split files using
Fastmerge
, and generated histograms for the merged k-mer database:I noticed that there are no k-mers with a count lower than 4 in the merged library histogram. I repeated the process a few times, combining different files, and the merged histograms consistently lack smaller k-mer counts (i.e., they start at 4 or 5). I’m unsure if this behavior is expected, as I do not understand why there are no single-occurrence k-mers. Is this a bug, or am I misunderstanding or misusing the tool?
Thanks for your assistance!
The text was updated successfully, but these errors were encountered: