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Thank you very much for the development of metawrap.
I have completed the analysis according to the tutorial, and I have a question about Step 8.
Assume that I have 3 samples (for example, sample A, sample B, sample C). At the beginning, all R1 and R2 are concatenated, and the BIN_REASSEMBLY folder is generated in Step 8, and the reassembled_bins in it is used for taxonomic naming in Step 9.
Then my question is, if BIN_REASSEMBLY/reassembled_bins/bin.1.strict.fa is the combined assembly result containing all these three samples, how to split bin.1.strict.fa into results like
bin.1.strict_sample A.fa
bin.1.strict_sample B.fa
bin.1.strict_sample C.fa
according to the marker or index?
Because I found that the classified microorganisms (based on Step 9) represented by bin1 have differences in abundance in the heat map of bin_abundance_heatmap.png (via Step 7), and I want to compare it with the reference genome to see the differences at the nucleotide level.
Hope to get your advice. Thank you in advance for taking the time to check
Best regards,
Chris
The text was updated successfully, but these errors were encountered:
Dear Developers
Thank you very much for the development of metawrap.
I have completed the analysis according to the tutorial, and I have a question about Step 8.
Assume that I have 3 samples (for example, sample A, sample B, sample C). At the beginning, all R1 and R2 are concatenated, and the BIN_REASSEMBLY folder is generated in Step 8, and the reassembled_bins in it is used for taxonomic naming in Step 9.
Then my question is, if BIN_REASSEMBLY/reassembled_bins/bin.1.strict.fa is the combined assembly result containing all these three samples, how to split bin.1.strict.fa into results like
bin.1.strict_sample A.fa
bin.1.strict_sample B.fa
bin.1.strict_sample C.fa
according to the marker or index?
Because I found that the classified microorganisms (based on Step 9) represented by bin1 have differences in abundance in the heat map of bin_abundance_heatmap.png (via Step 7), and I want to compare it with the reference genome to see the differences at the nucleotide level.
Hope to get your advice. Thank you in advance for taking the time to check
Best regards,
Chris
The text was updated successfully, but these errors were encountered: