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When passing a sorted bed file containing more than 20 billion lines of genomic regions to getfasta, I only got the results of chr1, chr10 and chr11. The rows behind them were ignored. By the way, I'm sure the RAM is abundant (1TB 3200MHz).
I searched the closed issues and bedtools documentation but didn't get a proper answer. I know I can avoid this by separating single file to multiple small files, but I'm just curious that does bedtools have a line limit which is not described in the doc, or it's more likely to be a buffer/tmp file issue on my Ubuntu server?
Thanks for your help in advance.
The text was updated successfully, but these errors were encountered:
When passing a sorted bed file containing more than 20 billion lines of genomic regions to getfasta, I only got the results of chr1, chr10 and chr11. The rows behind them were ignored. By the way, I'm sure the RAM is abundant (1TB 3200MHz).
I searched the closed issues and bedtools documentation but didn't get a proper answer. I know I can avoid this by separating single file to multiple small files, but I'm just curious that does bedtools have a line limit which is not described in the doc, or it's more likely to be a buffer/tmp file issue on my Ubuntu server?
Thanks for your help in advance.
The text was updated successfully, but these errors were encountered: