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Thanks for developing Strainy!
I'm trying to use amplicon-based Nanopore reads to figure out strain abundances in bacterial samples. The pool has 740 strains and each sample may contain ~10 of them. I have the reference sequences of all these strains. I've been calculating the abundances based the alignments after stringent filtering to exclude potential sequencing errors. I'd like to try Strainy to see if I can get better results.
Since I already have the strain references, I will use these sequences as the input to Strainy, but wonder whether Strainy has the resolution to distinguish two strains if they differ only at a couple of SNVs.
The text was updated successfully, but these errors were encountered:
weishwu
changed the title
Work with known strain references
Work with 740 known strain references with high similarity
Nov 8, 2024
weishwu
changed the title
Work with 740 known strain references with high similarity
amplicon ONT sequencing of 740 known strains
Nov 8, 2024
A couple of SNVs would be tricky for strainy. If they are close enough on the same unitig, strainy may be able to phase that unitig but if they are far apart, it would be more difficult.
If that doesn't work, you may try using one of the single strain references as the input.
Thanks for developing Strainy!
I'm trying to use amplicon-based Nanopore reads to figure out strain abundances in bacterial samples. The pool has 740 strains and each sample may contain ~10 of them. I have the reference sequences of all these strains. I've been calculating the abundances based the alignments after stringent filtering to exclude potential sequencing errors. I'd like to try Strainy to see if I can get better results.
Since I already have the strain references, I will use these sequences as the input to Strainy, but wonder whether Strainy has the resolution to distinguish two strains if they differ only at a couple of SNVs.
The text was updated successfully, but these errors were encountered: