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And one more thing, How did you calculated the QV of corrected reads? - as far as i know the output format of corrected reads is .fasta which does not have QV. I'm sorry if i'm wrong about this.
The text was updated successfully, but these errors were encountered:
Please try again with the following: wget -O HG002.experimentalUL.corrected.fasta.gz https://zenodo.org/records/13252378/files/HG002.experimentalUL.corrected.fasta.gz?download=1
Regarding QV,
The corrected reads themselves do not carry information about their quality.
We obtained some form of measurement of the quality of reads via two ways:
Aligning the reads to a high quality assembly of the same sample (if one exists) and measure the agreement between these reads and the aligned-to segment (e.g. using bamConcordance (https://github.com/PacificBiosciences/hg002-ccs/blob/master/concordance/bamConcordance) to get some form of Phred-scaled score, or just calculate accuracy from the CIGAR string).
I've tried to download your corrected data via:
wget http://complex.zesoi.fer.hr/data/downloads/HG002.experimentalUL.corrected.fasta.gz
But it doesn't seem like work and i could not download the data. Could you check the link again?
And one more thing, How did you calculated the QV of corrected reads? - as far as i know the output format of corrected reads is .fasta which does not have QV. I'm sorry if i'm wrong about this.
The text was updated successfully, but these errors were encountered: