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Description
Example for sample 1000392567 sequenced in the run 180321_M02081_0277_000000000-BN2F5-4:
There is a three nucleotide deletion in the consensus:
>v3_consensus
TGTACAAGACCCAACAACAATACAAGAAGAAGTATACATATAGGACCAGGGARARCATTT
TATGGAACA---AYARKAGGAGATATAAGACAAGCACATTGT
This deletion is only present in low frequency haplotypes:
>v3_haplotype_1-support_0.57
TGTACAAGACCCAACAACAATACAAGAAGAAGTATACATATAGGACCAGGGAGAGCATTT
TATGGAACAGACATAATAGGAGATATAAGACAAGCACATTGT
>v3_haplotype_2-support_0.20
TGTACAAGACCCAACAACAATACAAGAAGAAGTATACATATAGGACCAGGGAAAGCATTT
TATGGAACAGACATAATAGGAGATATAAGACAAGCACATTGT
>v3_haplotype_3-support_0.12
TGTACAAGACCCGGCAAGAAGAAAATAAGAATGATACATATAGGACCAGGGAGAACATTT
TATGGAACA---ACAGGAGGAGATATAAGACAAGCACATTGT
...
Is it maybe because that deletion is present at a frequency >15% and somehow "overwrites" the nucleotides at that position?
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