Comments (2)
I think it's due to the FM Index occupying too much memory, which is not highly optimized for big genomes. You can try removing -F
, which should use lesser RAM.
Besides, -V 0
is not necessary, which check the whole sequences before computing reverse complement sequences.
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Wow that made a big difference - only 2.6GB now. Thanks as always for the awesome tools @shenwei356
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Related Issues (20)
- Seqkit seq -r -p -t dna of file containing 16bp multiple sequences creates concatenated rev comp sequence. HOT 1
- Default to not removing ‘*’ for seqkit sum of peptides? HOT 2
- `seqkit subseq` with bed file does properly handle uppercase and lowercase accession (not case-sensitive?) HOT 4
- using seqkit locate for k-mer counting HOT 2
- Remove reads with certain amount of ambiguous bases HOT 2
- seqkit 2.5.0 reports wrong version number (2.4.0) HOT 2
- Possible bug in seqkit stats HOT 2
- Allow grep to handle pair suffix in ID HOT 2
- Fast way to run seqkit locate HOT 1
- Issue with sequence of length 1 and quality '+' HOT 3
- convert paired-end FASTQ to FASTA and split in one step HOT 3
- Exit status 141 running sample and head HOT 1
- Add average quality score to `stats` HOT 5
- Add subseq selected coordinates to FASTA? HOT 2
- [INFO] read BED file ... [ERRO] chr1: bad start: 144008994
- Retrieve the nucleotide sequences initially used from the SeqIDs of the protein sequences (question) HOT 9
- seqkit common/seqkit grep HOT 3
- How to calculate the length of GC content? HOT 2
- [feature suggestion] Reverse translate protein search expression into nucleotide regex or degenerate base sequence HOT 2
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