If I am working on Sanger sequencing results for a certain type of viruses, by assays that target parts of the genome, so I am using few assays for each sample, got a couple of sequencing reads for each sample. Then, assembly, MSA, then phylogenetics: Please, is there any recommended minimum sequence length (seq, bases number) for each read to consider it successful?, for example if after trimming of the low quality ends, I got read with 35 bp length?? can I consider it a successful sequencing? and can I use that read in MSA etc? of note, the other reads are of hundreds length.