Comments (1)
I got it to work! I went back and installed the tool through Git and was able to set the two files to 5x coverage! (I also had to unzip the files, but it worked!)
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Related Issues (20)
- Lower than expected coverage for illumina paired end reads HOT 9
- Suggestion: replace needletail by noodles and niffler HOT 1
- `HashSet` is slow HOT 3
- Compress output when requested HOT 5
- Input parameter for number of bases in addition to coverage and genome size HOT 6
- Calculate genome size from an index file HOT 1
- Add number and fraction options
- Docker image issue HOT 9
- Suggestion: Raise warning when desired level of coverage is not possible HOT 1
- Feature: Min/max coverage threshold HOT 2
- Multi-threading approach HOT 7
- Does rasusa outputs reads that still cover the entire original genome? HOT 1
- Random sampling based on bases for the metagenomic dataset HOT 1
- illumina read input error HOT 2
- Question: there is a way to start from a bam file instead of a fastq? HOT 1
- Generating only half of the target depth HOT 6
- Error: unable to gather read lengths for the first input file HOT 2
- Error HOT 1
- Error when using --output twice HOT 2
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