Hi, I have a whole c hromosome sequenced. as a result, I got a gapped sequence, some parts with 500-600 reads, and some contigs with only 8-9 reads. How reliable are these parts? Is there a minimum number of reads what I can accept as a good result, or I can take the 8-9x read parts as well if I want to submit a new sequence?
SEQUENCING - how to understand the results?
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