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. 2019 Sep 9;374(1784):20190194. doi: 10.1098/rstb.2019.0194

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© 2019 The Authors.

Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

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Figure 5. — Oxford Nanopore sequencing of gDNA. (a) Mapping of Mile-ap3a and Mile-ap3b onto a single Oxford Nanopore read. (b,c) RNAi knock-down of Mile-ap3a and in situ hybridization with a probe of Mile-ap3b. mult. aln., multiple alignments. (d,e) RNAi knock-down of Mile-ap3b and in situ hybridization with a probe of Mile-ap3a. (f) Dot plot of a nine kb section of genomic read ‘27752bc6-c8c2-433f-8100-0d294e375058’. (g) Hypothetical adhesive protein containing Mile-ap3a and Mile-ap3b and an extensive GRK low complexity region. (h) Mapping of Mile-ap2a and Mile-ap2b onto a single Oxford Nanopore read. (i,j) RNAi knock-down of Mile-ap2a and in situ hybridization with a probe of Mile-ap2b. (k) Dot plot of a 20 kb section of genomic read ‘7de1b9a2-7996-4a1a-8b10-3f661449fd01’. (l) Hypothetical adhesive protein containing Mile-ap2a and Mile-ap2b and 12 repeats of Mile-ap2a. ISH, in situ hybridization.