Selected article for: "protein sequence and supplementary table"

Author: Lara Urban; Andre Holzer; J Jotautas Baronas; Michael Hall; Philipp Braeuninger-Weimer; Michael J Scherm; Daniel J Kunz; Surangi N Perera; Daniel E Martin-Herranz; Edward T Tipper; Susannah J Salter; Maximilian R Stammnitz
Title: Freshwater monitoring by nanopore sequencing
  • Document date: 2020_2_7
  • ID: 77nsidzc_40
    Snippet: DNA extracts from each sampling batch and DI water control were separately amplified with V1-V9 full-length Figure 1b-c) , which was previously assessed using nanopore shotgun metagenomics 42 . We used common primer binding sequences 27f and 1492r, both coupled to unique 24 bp barcodes and a nanopore motor protein tether sequence (Supplementary Table 7 ). Fulllength 16S rDNA PCRs were performed with the following conditions: Table S2b ). We used .....
    Document: DNA extracts from each sampling batch and DI water control were separately amplified with V1-V9 full-length Figure 1b-c) , which was previously assessed using nanopore shotgun metagenomics 42 . We used common primer binding sequences 27f and 1492r, both coupled to unique 24 bp barcodes and a nanopore motor protein tether sequence (Supplementary Table 7 ). Fulllength 16S rDNA PCRs were performed with the following conditions: Table S2b ). We used KAPA Pure Beads (KAPA Biosystems, Wilmington, MA, USA) to concentrate full-length 16S rDNA products in 21 µL DI water. Multiplexed nanopore ligation sequencing libraries were then made by following the SQK-LSK109 protocol (Oxford Nanopore Technologies, Oxford, UK).

    Search related documents:
    Co phrase search for related documents
    • bp barcode and sequencing library: 1
    • di water and Supplementary table: 1, 2
    • di water and water control: 1
    • motor protein and Supplementary table: 1
    • rdna pcr and Supplementary table: 1
    • sequencing library and Supplementary table: 1, 2, 3, 4, 5
    • sequencing library and water control: 1
    • Supplementary table and water control: 1, 2