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I'm wondering why I'm encountering numerous short sequences in the stable fa (<100bp, >10,000 sequences). Additionally, I've noticed multiple headers in a single fa sequence.
Do you recommend any quality control steps after constructing the minigraph?
I used minigraph to generate an interactive GFA file for 50 genomes:
Hi @lh3,
I'm wondering why I'm encountering numerous short sequences in the stable fa (<100bp, >10,000 sequences). Additionally, I've noticed multiple headers in a single fa sequence.
Do you recommend any quality control steps after constructing the minigraph?
I used minigraph to generate an interactive GFA file for 50 genomes:
sample stable.fa
`>Bna.1SN01.A01_49059_49213 >N1:33431 >N1:33605
TACAAACATGGCTGTGCATATGATATTATAATTGTTAGCTGGTATTCAATTGATTTTGTAAGTTATTATATACACCCCATACTCAAGACTCTTAAGAATTTGTTGTTGTTGTACGAGACTGTTAGCATGTTAAAGATTGACCCCAAAAAAAAAA
Thanks
sam
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