A genome assembler that reduces the computational time of human genome assembly from 400,000 CPU hours to 2,000 CPU hours, utilizing long erroneous 3GS sequencing reads and short accurate NGS sequencing reads.
This will open and close the file each time it is needed. Might create additional IO overhead, but ulimit can be left intact. Very handy when you're not root.
The file DBG2OLC/utility/split_reads_by_backbone.py can be changed to this (line 118 and further):
This will open and close the file each time it is needed. Might create additional IO overhead, but ulimit can be left intact. Very handy when you're not root.