Hello, I am new in bioinformatics and I don´t have much idea in working with bacteria DNA data. I made 2 runs of Iluminaseq of different soil samples and i recieved all the results with the feature analysis done. Now i want to merge all the samples but i don´t know how to proceed. I obtained for the two runs a denoising_table.qza with the frecuencies of the ASVs which IDs are indentified like this (6e7604ec6f61c2fee0d97a8d8b3d057d...), a feature_table.qza in which features are identified like this (ASV1,ASV2...), a feature_sequence.qza that has a fasta document that especifies the secuence of each ASV identified in the same way as the feature_table and finally the taxonomy asigned to each ASV.
If I use the denoising tables to merge de runs i obtain the result that i want buecause the IDs of both tables refer to the same secuences but I dont know how to merge the secuences as they are identified with other labels (ASV1,ASV2...). If anyone can tell me how I should proceed I would appreciate it.