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when the genome contig are longer than 536,870,912 bases, samtools will fail.
ftp://ftp.ensemblgenomes.org/pub/plants/release-38/fasta/hordeum_vulgare/dna/Hordeum_vulgare.Hv_IBSC_PGSB_v2.dna.toplevel.fa.gz
I have use the genome to assemble my reads,it failed to sort the bwa output bam file. so, the samtools whether support longer contig?
The text was updated successfully, but these errors were encountered:
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when the genome contig are longer than 536,870,912 bases, samtools will fail.
I have use the genome to assemble my reads,it failed to sort the bwa output bam file.
so, the samtools whether support longer contig?
The text was updated successfully, but these errors were encountered: