Oct 24, 2025

Public workspaceIDEEL: UNC Implementation of Targeted PX1 Sequencing- MIP to Nanopore

IDEEL: UNC Implementation of Targeted PX1 Sequencing- MIP to Nanopore
  • Infectious Disease Epidemiology and Ecology Lab1
  • 1Infectious Disease Epidemiology and Ecology Lab, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA
  • IDEEL
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Protocol CitationInfectious Disease Epidemiology and Ecology Lab 2025. IDEEL: UNC Implementation of Targeted PX1 Sequencing- MIP to Nanopore. protocols.io https://dx.doi.org/10.17504/protocols.io.yxmvmbbebg3p/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: October 17, 2025
Last Modified: October 24, 2025
Protocol Integer ID: 230584
Keywords: PCR, Barcoding, Nanopore Library preparation, Amplification, Adapter Ligation, targeted sequencing of the px1 locus, targeted sequencing, integrating molecular inversion probe, molecular inversion probe, nanopore the protocol, px1 locus, oxford nanopore, read sequencing, nanopore
Abstract
The protocol describes a novel workflow integrating Molecular Inversion Probes (MIPs) with Oxford Nanopore long-read sequencing for targeted sequencing of the PX1 locus.
Materials
Required Materials:

  • Molecular Grade Water (MGW)
  • Primers

P2_Px1Block3_v2_F: GACTCGCCAAGCTGAAGNNNNAGAGAACAGGAAAAAGTTTGTACGT
P2_Px1Frag3_v8_R: ACGTGTGCTCTTCCGATCTNNNNTCATCACTGTCGCTACTTTTGTC

  • ReagentGoTaq® Long PCR Master Mix, 2XPromegaCatalog #M402A
  • Illumina FWD and REV barcode primers
  • Gel electrophoresis reagents and equipment.
  • 1X TE Low EDTA Buffer
  • PromethION 2 solo and device specific flow cells
  • ONT Ligation sequencing kit (SQK-LSK114 Kit)


PCR Round 2 Primers
Forward Primers:

Well PositionNameSequence
A01hybrid_dual_fw_001AATGATACGGCGACCACCGAGATCTACACGTTAAGACACACTCTTTCCCTACACGACTCGCCAAGCTGA
A02hybrid_dual_fw_002AATGATACGGCGACCACCGAGATCTACACTCTAAGTTACACTCTTTCCCTACACGACTCGCCAAGCTGA
A03hybrid_dual_fw_003AATGATACGGCGACCACCGAGATCTACACTGTACATTACACTCTTTCCCTACACGACTCGCCAAGCTGA
A04hybrid_dual_fw_004AATGATACGGCGACCACCGAGATCTACACAATACCGCACACTCTTTCCCTACACGACTCGCCAAGCTGA
A05hybrid_dual_fw_005AATGATACGGCGACCACCGAGATCTACACTGTCTATGACACTCTTTCCCTACACGACTCGCCAAGCTGA
A06hybrid_dual_fw_006AATGATACGGCGACCACCGAGATCTACACTCACTGTTACACTCTTTCCCTACACGACTCGCCAAGCTGA
A07hybrid_dual_fw_007AATGATACGGCGACCACCGAGATCTACACTTGTATTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
A08hybrid_dual_fw_008AATGATACGGCGACCACCGAGATCTACACAGACTAACACACTCTTTCCCTACACGACTCGCCAAGCTGA
A09hybrid_dual_fw_009AATGATACGGCGACCACCGAGATCTACACATTGTCAAACACTCTTTCCCTACACGACTCGCCAAGCTGA
A10hybrid_dual_fw_010AATGATACGGCGACCACCGAGATCTACACGTTCTACAACACTCTTTCCCTACACGACTCGCCAAGCTGA
A11hybrid_dual_fw_011AATGATACGGCGACCACCGAGATCTACACTTCATTCGACACTCTTTCCCTACACGACTCGCCAAGCTGA
A12hybrid_dual_fw_012AATGATACGGCGACCACCGAGATCTACACAAGCGTCAACACTCTTTCCCTACACGACTCGCCAAGCTGA
B01hybrid_dual_fw_013AATGATACGGCGACCACCGAGATCTACACCGTAGGATACACTCTTTCCCTACACGACTCGCCAAGCTGA
B02hybrid_dual_fw_014AATGATACGGCGACCACCGAGATCTACACAGTTAGCGACACTCTTTCCCTACACGACTCGCCAAGCTGA
B03hybrid_dual_fw_015AATGATACGGCGACCACCGAGATCTACACGAACGTCTACACTCTTTCCCTACACGACTCGCCAAGCTGA
B04hybrid_dual_fw_016AATGATACGGCGACCACCGAGATCTACACAGAACACTACACTCTTTCCCTACACGACTCGCCAAGCTGA
B05hybrid_dual_fw_017AATGATACGGCGACCACCGAGATCTACACTGTTGGCAACACTCTTTCCCTACACGACTCGCCAAGCTGA
B06hybrid_dual_fw_018AATGATACGGCGACCACCGAGATCTACACGGCTAATAACACTCTTTCCCTACACGACTCGCCAAGCTGA
B07hybrid_dual_fw_019AATGATACGGCGACCACCGAGATCTACACGCTAGAATACACTCTTTCCCTACACGACTCGCCAAGCTGA
B08hybrid_dual_fw_020AATGATACGGCGACCACCGAGATCTACACTGTACTAAACACTCTTTCCCTACACGACTCGCCAAGCTGA
B09hybrid_dual_fw_021AATGATACGGCGACCACCGAGATCTACACAGTTACACACACTCTTTCCCTACACGACTCGCCAAGCTGA
B10hybrid_dual_fw_022AATGATACGGCGACCACCGAGATCTACACGTACACGAACACTCTTTCCCTACACGACTCGCCAAGCTGA
B11hybrid_dual_fw_023AATGATACGGCGACCACCGAGATCTACACACTGTAAGACACTCTTTCCCTACACGACTCGCCAAGCTGA
B12hybrid_dual_fw_024AATGATACGGCGACCACCGAGATCTACACGATCATGAACACTCTTTCCCTACACGACTCGCCAAGCTGA
C01hybrid_dual_fw_025AATGATACGGCGACCACCGAGATCTACACTGCTAACGACACTCTTTCCCTACACGACTCGCCAAGCTGA
C02hybrid_dual_fw_026AATGATACGGCGACCACCGAGATCTACACTAATGCTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
C03hybrid_dual_fw_027AATGATACGGCGACCACCGAGATCTACACCTTGTTGAACACTCTTTCCCTACACGACTCGCCAAGCTGA
C04hybrid_dual_fw_028AATGATACGGCGACCACCGAGATCTACACGATACAAGACACTCTTTCCCTACACGACTCGCCAAGCTGA
C05hybrid_dual_fw_029AATGATACGGCGACCACCGAGATCTACACATACAGCGACACTCTTTCCCTACACGACTCGCCAAGCTGA
C06hybrid_dual_fw_030AATGATACGGCGACCACCGAGATCTACACCTGGATAGACACTCTTTCCCTACACGACTCGCCAAGCTGA
C07hybrid_dual_fw_031AATGATACGGCGACCACCGAGATCTACACTCATCAGCACACTCTTTCCCTACACGACTCGCCAAGCTGA
C08hybrid_dual_fw_032AATGATACGGCGACCACCGAGATCTACACTTATACCGACACTCTTTCCCTACACGACTCGCCAAGCTGA
C09hybrid_dual_fw_033AATGATACGGCGACCACCGAGATCTACACGCTGATTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
C10hybrid_dual_fw_034AATGATACGGCGACCACCGAGATCTACACATAAGGCCACACTCTTTCCCTACACGACTCGCCAAGCTGA
C11hybrid_dual_fw_035AATGATACGGCGACCACCGAGATCTACACAAGACTAGACACTCTTTCCCTACACGACTCGCCAAGCTGA
C12hybrid_dual_fw_036AATGATACGGCGACCACCGAGATCTACACTAGCAACAACACTCTTTCCCTACACGACTCGCCAAGCTGA
D01hybrid_dual_fw_037AATGATACGGCGACCACCGAGATCTACACCAAGTAATACACTCTTTCCCTACACGACTCGCCAAGCTGA
D02hybrid_dual_fw_038AATGATACGGCGACCACCGAGATCTACACTCATGATGACACTCTTTCCCTACACGACTCGCCAAGCTGA
D03hybrid_dual_fw_039AATGATACGGCGACCACCGAGATCTACACTAGCTCTTACACTCTTTCCCTACACGACTCGCCAAGCTGA
D04hybrid_dual_fw_040AATGATACGGCGACCACCGAGATCTACACACTACATGACACTCTTTCCCTACACGACTCGCCAAGCTGA
D05hybrid_dual_fw_041AATGATACGGCGACCACCGAGATCTACACTGTGCCATACACTCTTTCCCTACACGACTCGCCAAGCTGA
D06hybrid_dual_fw_042AATGATACGGCGACCACCGAGATCTACACGACTTCCAACACTCTTTCCCTACACGACTCGCCAAGCTGA
D07hybrid_dual_fw_043AATGATACGGCGACCACCGAGATCTACACTATTCTCGACACTCTTTCCCTACACGACTCGCCAAGCTGA
D08hybrid_dual_fw_044AATGATACGGCGACCACCGAGATCTACACCACTAGATACACTCTTTCCCTACACGACTCGCCAAGCTGA
D09hybrid_dual_fw_045AATGATACGGCGACCACCGAGATCTACACCTTCGCATACACTCTTTCCCTACACGACTCGCCAAGCTGA
D10hybrid_dual_fw_046AATGATACGGCGACCACCGAGATCTACACCTAGCGATACACTCTTTCCCTACACGACTCGCCAAGCTGA
D11hybrid_dual_fw_047AATGATACGGCGACCACCGAGATCTACACTACGTTAAACACTCTTTCCCTACACGACTCGCCAAGCTGA
D12hybrid_dual_fw_048AATGATACGGCGACCACCGAGATCTACACAAGTAGTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
E01hybrid_dual_fw_049AATGATACGGCGACCACCGAGATCTACACGACGTATCACACTCTTTCCCTACACGACTCGCCAAGCTGA
E02hybrid_dual_fw_050AATGATACGGCGACCACCGAGATCTACACACGTTCAGACACTCTTTCCCTACACGACTCGCCAAGCTGA
E03hybrid_dual_fw_051AATGATACGGCGACCACCGAGATCTACACAGCTATATACACTCTTTCCCTACACGACTCGCCAAGCTGA
E04hybrid_dual_fw_052AATGATACGGCGACCACCGAGATCTACACAGTGCGAAACACTCTTTCCCTACACGACTCGCCAAGCTGA
E05hybrid_dual_fw_053AATGATACGGCGACCACCGAGATCTACACCAATGGTAACACTCTTTCCCTACACGACTCGCCAAGCTGA
E06hybrid_dual_fw_054AATGATACGGCGACCACCGAGATCTACACATTCCGATACACTCTTTCCCTACACGACTCGCCAAGCTGA
E07hybrid_dual_fw_055AATGATACGGCGACCACCGAGATCTACACAGCTGTTGACACTCTTTCCCTACACGACTCGCCAAGCTGA
E08hybrid_dual_fw_056AATGATACGGCGACCACCGAGATCTACACTTCGACTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
E09hybrid_dual_fw_057AATGATACGGCGACCACCGAGATCTACACCGAATGGTACACTCTTTCCCTACACGACTCGCCAAGCTGA
E10hybrid_dual_fw_058AATGATACGGCGACCACCGAGATCTACACTAGTGTACACACTCTTTCCCTACACGACTCGCCAAGCTGA
E11hybrid_dual_fw_059AATGATACGGCGACCACCGAGATCTACACACGCATGAACACTCTTTCCCTACACGACTCGCCAAGCTGA
E12hybrid_dual_fw_060AATGATACGGCGACCACCGAGATCTACACTTCGTACAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F01hybrid_dual_fw_061AATGATACGGCGACCACCGAGATCTACACTTCTGCTAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F02hybrid_dual_fw_062AATGATACGGCGACCACCGAGATCTACACTGGAAGCAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F03hybrid_dual_fw_063AATGATACGGCGACCACCGAGATCTACACGATGCTCAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F04hybrid_dual_fw_064AATGATACGGCGACCACCGAGATCTACACAGCCTGAAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F05hybrid_dual_fw_065AATGATACGGCGACCACCGAGATCTACACCACCAGTAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F06hybrid_dual_fw_066AATGATACGGCGACCACCGAGATCTACACGTTACACCACACTCTTTCCCTACACGACTCGCCAAGCTGA
F07hybrid_dual_fw_067AATGATACGGCGACCACCGAGATCTACACGCGTTAGTACACTCTTTCCCTACACGACTCGCCAAGCTGA
F08hybrid_dual_fw_068AATGATACGGCGACCACCGAGATCTACACTGACGTTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
F09hybrid_dual_fw_069AATGATACGGCGACCACCGAGATCTACACTAGGCGTAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F10hybrid_dual_fw_070AATGATACGGCGACCACCGAGATCTACACAAGTGAGCACACTCTTTCCCTACACGACTCGCCAAGCTGA
F11hybrid_dual_fw_071AATGATACGGCGACCACCGAGATCTACACCCGGAATAACACTCTTTCCCTACACGACTCGCCAAGCTGA
F12hybrid_dual_fw_072AATGATACGGCGACCACCGAGATCTACACAATAGGCAACACTCTTTCCCTACACGACTCGCCAAGCTGA
G01hybrid_dual_fw_073AATGATACGGCGACCACCGAGATCTACACTTCAGGTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
G02hybrid_dual_fw_074AATGATACGGCGACCACCGAGATCTACACTAATCGCTACACTCTTTCCCTACACGACTCGCCAAGCTGA
G03hybrid_dual_fw_075AATGATACGGCGACCACCGAGATCTACACCTTAGGTGACACTCTTTCCCTACACGACTCGCCAAGCTGA
G04hybrid_dual_fw_076AATGATACGGCGACCACCGAGATCTACACTTGATCTCACACTCTTTCCCTACACGACTCGCCAAGCTGA
G05hybrid_dual_fw_077AATGATACGGCGACCACCGAGATCTACACTCTTACTGACACTCTTTCCCTACACGACTCGCCAAGCTGA
G06hybrid_dual_fw_078AATGATACGGCGACCACCGAGATCTACACGAGTACACACACTCTTTCCCTACACGACTCGCCAAGCTGA
G07hybrid_dual_fw_079AATGATACGGCGACCACCGAGATCTACACACGTTACAACACTCTTTCCCTACACGACTCGCCAAGCTGA
G08hybrid_dual_fw_080AATGATACGGCGACCACCGAGATCTACACTGGTAAGCACACTCTTTCCCTACACGACTCGCCAAGCTGA
G09hybrid_dual_fw_081AATGATACGGCGACCACCGAGATCTACACGATAGCACACACTCTTTCCCTACACGACTCGCCAAGCTGA
G10hybrid_dual_fw_082AATGATACGGCGACCACCGAGATCTACACGACTTAGGACACTCTTTCCCTACACGACTCGCCAAGCTGA
G11hybrid_dual_fw_083AATGATACGGCGACCACCGAGATCTACACAGTCGTTAACACTCTTTCCCTACACGACTCGCCAAGCTGA
G12hybrid_dual_fw_084AATGATACGGCGACCACCGAGATCTACACCGTGATTAACACTCTTTCCCTACACGACTCGCCAAGCTGA
H01hybrid_dual_fw_085AATGATACGGCGACCACCGAGATCTACACTCAGTAGAACACTCTTTCCCTACACGACTCGCCAAGCTGA
H02hybrid_dual_fw_086AATGATACGGCGACCACCGAGATCTACACATGTGTCTACACTCTTTCCCTACACGACTCGCCAAGCTGA
H03hybrid_dual_fw_087AATGATACGGCGACCACCGAGATCTACACCAGAATATACACTCTTTCCCTACACGACTCGCCAAGCTGA
H04hybrid_dual_fw_088AATGATACGGCGACCACCGAGATCTACACTAAGTCTGACACTCTTTCCCTACACGACTCGCCAAGCTGA
H05hybrid_dual_fw_089AATGATACGGCGACCACCGAGATCTACACATCGACATACACTCTTTCCCTACACGACTCGCCAAGCTGA
H06hybrid_dual_fw_090AATGATACGGCGACCACCGAGATCTACACACAGCTGTACACTCTTTCCCTACACGACTCGCCAAGCTGA
H07hybrid_dual_fw_091AATGATACGGCGACCACCGAGATCTACACATCACAAGACACTCTTTCCCTACACGACTCGCCAAGCTGA
H08hybrid_dual_fw_092AATGATACGGCGACCACCGAGATCTACACGTCGAATTACACTCTTTCCCTACACGACTCGCCAAGCTGA
H09hybrid_dual_fw_093AATGATACGGCGACCACCGAGATCTACACTGCCGATTACACTCTTTCCCTACACGACTCGCCAAGCTGA
H10hybrid_dual_fw_094AATGATACGGCGACCACCGAGATCTACACACTAATGCACACTCTTTCCCTACACGACTCGCCAAGCTGA
H11hybrid_dual_fw_095AATGATACGGCGACCACCGAGATCTACACCTAGTAGGACACTCTTTCCCTACACGACTCGCCAAGCTGA
H12hybrid_dual_fw_096AATGATACGGCGACCACCGAGATCTACACTTAAGCCAACACTCTTTCCCTACACGACTCGCCAAGCTGA


Reverse Primers

Well PositionNameSequence
A01hybrid_dual_rev_001CAAGCAGAAGACGGCATACGAGATGTTAAGACGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A02hybrid_dual_rev_002CAAGCAGAAGACGGCATACGAGATTCTAAGTTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A03hybrid_dual_rev_003CAAGCAGAAGACGGCATACGAGATTGTACATTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A04hybrid_dual_rev_004CAAGCAGAAGACGGCATACGAGATAATACCGCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A05hybrid_dual_rev_005CAAGCAGAAGACGGCATACGAGATTGTCTATGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A06hybrid_dual_rev_006CAAGCAGAAGACGGCATACGAGATTCACTGTTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A07hybrid_dual_rev_007CAAGCAGAAGACGGCATACGAGATTTGTATTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A08hybrid_dual_rev_008CAAGCAGAAGACGGCATACGAGATAGACTAACGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A09hybrid_dual_rev_009CAAGCAGAAGACGGCATACGAGATATTGTCAAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A10hybrid_dual_rev_010CAAGCAGAAGACGGCATACGAGATGTTCTACAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A11hybrid_dual_rev_011CAAGCAGAAGACGGCATACGAGATTTCATTCGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
A12hybrid_dual_rev_012CAAGCAGAAGACGGCATACGAGATAAGCGTCAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B01hybrid_dual_rev_013CAAGCAGAAGACGGCATACGAGATCGTAGGATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B02hybrid_dual_rev_014CAAGCAGAAGACGGCATACGAGATAGTTAGCGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B03hybrid_dual_rev_015CAAGCAGAAGACGGCATACGAGATGAACGTCTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B04hybrid_dual_rev_016CAAGCAGAAGACGGCATACGAGATAGAACACTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B05hybrid_dual_rev_017CAAGCAGAAGACGGCATACGAGATTGTTGGCAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B06hybrid_dual_rev_018CAAGCAGAAGACGGCATACGAGATGGCTAATAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B07hybrid_dual_rev_019CAAGCAGAAGACGGCATACGAGATGCTAGAATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B08hybrid_dual_rev_020CAAGCAGAAGACGGCATACGAGATTGTACTAAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B09hybrid_dual_rev_021CAAGCAGAAGACGGCATACGAGATAGTTACACGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B10hybrid_dual_rev_022CAAGCAGAAGACGGCATACGAGATGTACACGAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B11hybrid_dual_rev_023CAAGCAGAAGACGGCATACGAGATACTGTAAGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
B12hybrid_dual_rev_024CAAGCAGAAGACGGCATACGAGATGATCATGAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C01hybrid_dual_rev_025CAAGCAGAAGACGGCATACGAGATTGCTAACGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C02hybrid_dual_rev_026CAAGCAGAAGACGGCATACGAGATTAATGCTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C03hybrid_dual_rev_027CAAGCAGAAGACGGCATACGAGATCTTGTTGAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C04hybrid_dual_rev_028CAAGCAGAAGACGGCATACGAGATGATACAAGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C05hybrid_dual_rev_029CAAGCAGAAGACGGCATACGAGATATACAGCGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C06hybrid_dual_rev_030CAAGCAGAAGACGGCATACGAGATCTGGATAGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C07hybrid_dual_rev_031CAAGCAGAAGACGGCATACGAGATTCATCAGCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C08hybrid_dual_rev_032CAAGCAGAAGACGGCATACGAGATTTATACCGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C09hybrid_dual_rev_033CAAGCAGAAGACGGCATACGAGATGCTGATTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C10hybrid_dual_rev_034CAAGCAGAAGACGGCATACGAGATATAAGGCCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C11hybrid_dual_rev_035CAAGCAGAAGACGGCATACGAGATAAGACTAGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
C12hybrid_dual_rev_036CAAGCAGAAGACGGCATACGAGATTAGCAACAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D01hybrid_dual_rev_037CAAGCAGAAGACGGCATACGAGATCAAGTAATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D02hybrid_dual_rev_038CAAGCAGAAGACGGCATACGAGATTCATGATGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D03hybrid_dual_rev_039CAAGCAGAAGACGGCATACGAGATTAGCTCTTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D04hybrid_dual_rev_040CAAGCAGAAGACGGCATACGAGATACTACATGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D05hybrid_dual_rev_041CAAGCAGAAGACGGCATACGAGATTGTGCCATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D06hybrid_dual_rev_042CAAGCAGAAGACGGCATACGAGATGACTTCCAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D07hybrid_dual_rev_043CAAGCAGAAGACGGCATACGAGATTATTCTCGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D08hybrid_dual_rev_044CAAGCAGAAGACGGCATACGAGATCACTAGATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D09hybrid_dual_rev_045CAAGCAGAAGACGGCATACGAGATCTTCGCATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D10hybrid_dual_rev_046CAAGCAGAAGACGGCATACGAGATCTAGCGATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D11hybrid_dual_rev_047CAAGCAGAAGACGGCATACGAGATTACGTTAAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
D12hybrid_dual_rev_048CAAGCAGAAGACGGCATACGAGATAAGTAGTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E01hybrid_dual_rev_049CAAGCAGAAGACGGCATACGAGATGACGTATCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E02hybrid_dual_rev_050CAAGCAGAAGACGGCATACGAGATACGTTCAGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E03hybrid_dual_rev_051CAAGCAGAAGACGGCATACGAGATAGCTATATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E04hybrid_dual_rev_052CAAGCAGAAGACGGCATACGAGATAGTGCGAAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E05hybrid_dual_rev_053CAAGCAGAAGACGGCATACGAGATCAATGGTAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E06hybrid_dual_rev_054CAAGCAGAAGACGGCATACGAGATATTCCGATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E07hybrid_dual_rev_055CAAGCAGAAGACGGCATACGAGATAGCTGTTGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E08hybrid_dual_rev_056CAAGCAGAAGACGGCATACGAGATTTCGACTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E09hybrid_dual_rev_057CAAGCAGAAGACGGCATACGAGATCGAATGGTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E10hybrid_dual_rev_058CAAGCAGAAGACGGCATACGAGATTAGTGTACGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E11hybrid_dual_rev_059CAAGCAGAAGACGGCATACGAGATACGCATGAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
E12hybrid_dual_rev_060CAAGCAGAAGACGGCATACGAGATTTCGTACAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F01hybrid_dual_rev_061CAAGCAGAAGACGGCATACGAGATTTCTGCTAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F02hybrid_dual_rev_062CAAGCAGAAGACGGCATACGAGATTGGAAGCAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F03hybrid_dual_rev_063CAAGCAGAAGACGGCATACGAGATGATGCTCAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F04hybrid_dual_rev_064CAAGCAGAAGACGGCATACGAGATAGCCTGAAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F05hybrid_dual_rev_065CAAGCAGAAGACGGCATACGAGATCACCAGTAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F06hybrid_dual_rev_066CAAGCAGAAGACGGCATACGAGATGTTACACCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F07hybrid_dual_rev_067CAAGCAGAAGACGGCATACGAGATGCGTTAGTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F08hybrid_dual_rev_068CAAGCAGAAGACGGCATACGAGATTGACGTTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F09hybrid_dual_rev_069CAAGCAGAAGACGGCATACGAGATTAGGCGTAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F10hybrid_dual_rev_070CAAGCAGAAGACGGCATACGAGATAAGTGAGCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F11hybrid_dual_rev_071CAAGCAGAAGACGGCATACGAGATCCGGAATAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
F12hybrid_dual_rev_072CAAGCAGAAGACGGCATACGAGATAATAGGCAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G01hybrid_dual_rev_073CAAGCAGAAGACGGCATACGAGATTTCAGGTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G02hybrid_dual_rev_074CAAGCAGAAGACGGCATACGAGATTAATCGCTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G03hybrid_dual_rev_075CAAGCAGAAGACGGCATACGAGATCTTAGGTGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G04hybrid_dual_rev_076CAAGCAGAAGACGGCATACGAGATTTGATCTCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G05hybrid_dual_rev_077CAAGCAGAAGACGGCATACGAGATTCTTACTGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G06hybrid_dual_rev_078CAAGCAGAAGACGGCATACGAGATGAGTACACGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G07hybrid_dual_rev_079CAAGCAGAAGACGGCATACGAGATACGTTACAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G08hybrid_dual_rev_080CAAGCAGAAGACGGCATACGAGATTGGTAAGCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G09hybrid_dual_rev_081CAAGCAGAAGACGGCATACGAGATGATAGCACGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G10hybrid_dual_rev_082CAAGCAGAAGACGGCATACGAGATGACTTAGGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G11hybrid_dual_rev_083CAAGCAGAAGACGGCATACGAGATAGTCGTTAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
G12hybrid_dual_rev_084CAAGCAGAAGACGGCATACGAGATCGTGATTAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H01hybrid_dual_rev_085CAAGCAGAAGACGGCATACGAGATTCAGTAGAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H02hybrid_dual_rev_086CAAGCAGAAGACGGCATACGAGATATGTGTCTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H03hybrid_dual_rev_087CAAGCAGAAGACGGCATACGAGATCAGAATATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H04hybrid_dual_rev_088CAAGCAGAAGACGGCATACGAGATTAAGTCTGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H05hybrid_dual_rev_089CAAGCAGAAGACGGCATACGAGATATCGACATGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H06hybrid_dual_rev_090CAAGCAGAAGACGGCATACGAGATACAGCTGTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H07hybrid_dual_rev_091CAAGCAGAAGACGGCATACGAGATATCACAAGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H08hybrid_dual_rev_092CAAGCAGAAGACGGCATACGAGATGTCGAATTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H09hybrid_dual_rev_093CAAGCAGAAGACGGCATACGAGATTGCCGATTGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H10hybrid_dual_rev_094CAAGCAGAAGACGGCATACGAGATACTAATGCGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H11hybrid_dual_rev_095CAAGCAGAAGACGGCATACGAGATCTAGTAGGGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT
H12hybrid_dual_rev_096CAAGCAGAAGACGGCATACGAGATTTAAGCCAGTGACTGGAGTTCAGACGTGTGCTCTTCCGAT


Troubleshooting
Section 1: Preparation of PCR2 Primer plates
To allow for high levels of combinations of indexing primers, we generate multiple forward primer plates (12) from a single 96-well plate. By using these 12 plates in combination with a single 96-well plate of reverse primers, we can index 1,152 samples. Additional primers can be designed to increase this multiplexing. Here we present one plate of forward and one plate of reverse primers to allow for this level of combination.

To generate forward primer plates, we shift the column to the right one column when replating to a new plate (e.g. column 1 becomes column 2 and column 12 becomes column 1). See the figure below. Be sure to uniquely label the plate so you know which primers are used in library preparation.

Primer plate

Note
We do NOT do this for reverse primers.

Section 2: Generate Primers mix
10m
Spin lyophilized Primer.

Centrifigation
Resuspend in MGW using the provided volume for a Concentration100 micromolar (µM) stock.

Vortex and spin down briefly.

Centrifigation
Let the mixture sit for about Duration00:10:00 for complete dissolution.

10m
Prepare the stock primer pool (Concentration100 micromolar (µM) ) by mixing 1 volume of P2_Px1Block3_v2_F with 1 volume of P2_Px1Frag3_v8_R.

Dilute primer pool with MGW to obtain Concentration25 micromolar (µM) working solution: 1 volume of stock + 3 volumes of MGW.

Section 3: PCR1
Pre-set the thermocycler before starting master mix preparation using the programme below.
ABCD
StepTemperature (oC)Time (minute)Number of cycles
Step1 (preheat)95holdNA
Step2 (Activation)9502:00NA
Step3 (Denaturation)9400:30x32
Step4 (Annealing)6508:00x32^ go to step 3
Step5 (final Extension)7210:00NA
Step64holdNA
All sample plates and controls are to be kept on cold blocks - switch out cold blocks if they are getting warm.

All reagents are to be kept TemperatureOn ice and the tube used to prepare the master mix should also remain TemperatureOn ice .

Centrifuge sample plates at Centrifigation4000 rpm, 00:01:00 .

1m
Centrifigation
Prepare the master mix using the template (here 96 reactions) below and adjust it to the number of reactions.
ABC
Master Mixx1x96*1.1
Gotaq101056
Molecular grade water5.2549.12
Primer pool (P2_Px1Block3_v2_F and P2_Px1Frag3_v8_R)0.884.48
template DNA4
Divide the total master mix volume by 12 and aliquot the designated volume of into 12 tube strip on cold block to allow for multichannel pipetting.

Using a multichannel, pipette Amount16 µL of master mix into each well of 96 well plate..

Pipetting
Using a multichannel, plate Amount4 µL of sample into each well on the PCR1 plate.

Note
Add at least one positive control (lab strain, 4uL) and one PCR1 negative control (MGW, 4uL).

Pipetting
Centrifuge the plate at Centrifigation4000 rpm, 00:01:00 .

1m
Centrifigation
Place the plate in the thermocycler and start running the pre-set PCR program.

PCR
Section 4: PCR2 or barcoding PCR
Once the first PCR is complete, pre-set the thermocycler before starting the master mix preparation for PCR2 using the programme below.
ABCD
StepTemperature (oC)Time (minute)Number of cycles
Step198holdNA
Step2980:30NA
Step3950:10x10
Step4628:0x10
Step5720:20x10
Step6721:0NA
Step74holdNA
Prepare the master mix for PCR2 using the template (here 96 reactions) below and adjust it to the number of reactions.
ABC
Master mixx1x96*1.1
Gotaq101056
Molecular grade water6633.6
Divide the total master mix volume by 12 and aliquot the designated volume (Amount140.8 µL for 96 sample run) into 12 tube strip on cold block to allow for multichannel pipetting.

Using a multichannel, pipette Amount16 µL of master mix into each well.

Pipetting
Spin down the forward and reverse PCR2 primer plates needed for the experiment at Centrifigation4000 rpm, 00:01:00 and add Amount1 µL of forward primer and Amount1 µL of reverse primer into each well using the multichannel.

Note
On your sample sheet, please denote the name of the forward and reverse primer plate used and the well of the sample to be sure you know the correct index for the sample you are genotyping.

1m
Centrifigation
Pipetting
In the post-PCR lab, add Amount2 µL of the PCR1 product to the master mix using a multichannel.

Pipetting
Optional: shake the plate gently on a shaker for Duration00:01:00 to mix the master mix added to the samples.

1m
Optional
Centrifuge the plate at Centrifigation4000 rpm, 00:01:00 .

1m
Centrifigation
Place the plate in the thermocycler and start running the pre-set PCR program.

Note
Check a random set of 10 wells per plate for amplification by gel electrophoresis based on your lab protocol (including the NTC and positive control).

PCR
Section 5: PCR Product Pooling and Cleanup
Pool Amount5 µL of PCR2 product into a single Eppendorf tube. If the pool is very large, Amount3 µL is sufficient.

Pipetting
Bring Ampure Beads to TemperatureRoom temperature . The Bailey Lab makes their own bead solution with Spherotech beads (DIY).

Add an equal volume of beads to the pool (1X bead clean). Let it incubate for at least Duration00:10:00 at TemperatureRoom temperature . For a higher yield, place the tube on a Hula Mixer or invert it in your hand.

Incubation
Pipetting
Place the pool on a magnet and wait until the beads have pelletted on the magnet and the solution is clear. Prepare enough fresh 80% ethanol to cover the beads for 2 washes.

Remove the supernatant and reserve it in another tube.

Wash with 80% ethanol for at least Duration00:00:30 . Discard the ethanol.

Wash
Repeat the above step for a second wash.

Wash
Remove the ethanol and let the beads dry for around Duration00:01:00 (do not let the beads dry until cracking).

1m
Elute in Amount51 µL of 1X low EDTA TE Buffer. If the pool is very large, use your discretion and elute in a higher volume (we eluted in Amount150 µL with 6 96-well plates of sample). Incubate at TemperatureRoom temperature for Duration00:10:00 .

10m
Incubation
Pipetting
Pellet the beads on a magnet and remove the elution into another tube.

Quantify the elution with a Qubit fluorometer.

Section 6: Nanopore Library preparation
36m 30s

Note
We use the SQK-LSK114 Kit (Ligation Sequencing) and have adapted this protocol from the Ligation Sequencing Amplicons V14 protocol from Nanopore. We use the P2 sequencing machine, but this protocol could be adapted for Minion.

End Prep

Transfer 200 fmol of cleaned DNA into a PCR tube or plate. Calculation for fmol can be done on this website: https://www.promega.com/resources/tools/biomath/ (1 pmol = 1,000 fmol). Adjust the volume to Amount50 µL with nuclease-free water.

Pipetting
Add the following to a PCR tube:
AB
ReagentVolume
DNA Template50 uL
Ultra II End Prep Reaction Buffer7 uL
Ultra II End Prep Enzyme Mix3 uL
Total60uL
Pipetting
Mix thoroughly by pipetting.

Pipetting
Mix
Incubate at Temperature20 °C for Duration00:05:00 and Temperature65 °C for Duration00:05:00 .

10m
Incubation
Spin down and transfer the sample to a clean 1.5ml Eppendorf tube

Centrifigation
Pipetting
Bring beads to TemperatureRoom temperature and add Amount60 µL to the DNA sample.

Pipetting
Temperature
Incubate for Duration00:10:00 at TemperatureRoom temperature . For increased yield, place the tube on a Hula Mixer or invert in your hand. Meanwhile, prepare Amount1 mL of 80% ethanol.

10m
Incubation
Temperature
Pellet on a magnet and remove the supernatant - keep the supernatant for extra security.

Wash with Amount500 µL of 80% ethanol. Remove after Duration00:00:30 .

30s
Wash
Repeat the above step for a total of 2 washes.

Wash
Let the beads dry for around Duration00:01:00 . Do not let the beads crack on the side of the tube.

1m
Elute in Amount61 µL of nuclease-free water. Let it incubate at TemperatureRoom temperature for Duration00:05:00 .

5m
Incubation
Temperature
Pellet on the magnet and remove the elution.

Quantify the End-prepped DNA with a qubit fluorometer. This library can be stored at Temperature4 °C for short-term storage, or at Temperature-20 °C or Temperature-80 °C for long-term storage.

Adapter Ligation

Thaw the Short Fragment Buffer (SFB) and the Elution Buffer (EB) at TemperatureRoom temperature . Place the Ligation Adapter (LA), Ligation Buffer (LNB), and Quick T4 Ligase TemperatureOn ice .

Temperature
Mix the following in a 1.5 ml Eppendorf tube, mixing 10-20 times after each addition:
AB
ReagentVolume
End-prepped DNA60 uL
Ligation Buffer (LNB)25 uL
NEBNext Quick T4 Ligase10 uL
Ligation Adapter (LA)5 uL
Total100 uL
Mix
Mix well by pipetting. Incubate at TemperatureRoom temperature for at least Duration00:10:00 . A longer incubation of Duration00:20:00 will increase the amount of ligated adapters.

Incubation
Pipetting
Mix
Bring the beads to TemperatureRoom temperature and resuspend.

Temperature
Add Amount60 µL of beads and mix by inverting. Incubate for Duration00:10:00 at TemperatureRoom temperature . For higher yield, invert in your hand or place on a Hula mixer.

10m
Incubation
Pipetting
Mix
Pellet on a magnet and remove the supernatant.

Wash with Amount250 µL of the Short Fragment buffer. Remove after around Duration00:00:30 .

Wash
Repeat the above step for a total of 2 washes.

Wash
Allow beads to dry on the magnet, and pipette out any residual buffer. Do not let beads dry to the point of cracking.

Elute in Amount25 µL of the Elution Buffer (EB). Incubate for Duration00:10:00 at TemperatureRoom temperature .

Incubation
Temperature
Pellet on a magnet and pipette the elution into a tube (ideally a screw cap tube for best storage).

Pipetting
Quantify the library with a qubit fluorometer. Be sure that you have at least 120 fmol of DNA, which is around Amount25 ng of DNA for a 4CAST library. This library can be stored at Temperature4 °C for short-term storage, or at Temperature-20 °C or Temperature-80 °C for long-term storage.

Section 7: Nanopore sequencing
1h 15m
Loading the Flow Cell

Take the Promethion Flow Cell you plan to use out of the Temperature4 °C refrigerator at least Duration00:20:00 before use. It is highly recommended to do a flow cell check before any sequencing.

Determine 100 - 120 fmols of library and add to an Eppendorf tube (Nanopore recommends 20 fmol for sequencing; however, this leads to underloading of the flow cell in most cases. If you have less than 100 fmols, add the entire library). Amount25 ng of 4CAST Library is around 120 fmols.

Pipetting
Bring up the 100 - 120 fmols of library to Amount32 µL with the elution buffer (EB).

After Duration00:20:00 at TemperatureRoom temperature , gently insert the flow cell into one of the ports of the P2. The lights will turn blue if inserted correctly, and red if inserted incorrectly.

In a 1.5 Eppendorf tube, mix the following to create the flow cell priming mix:
AB
ReagentVolume
Flow Cell Flush (FCF)1170 uL
Flow Cell Tether (FCT)30 uL
Total1200 uL
Mix
Set a P1000 pipette to 200. Open the inlet port and place the tip inside the port. Turn the dial until it shows 220-230. A small amount of buffer should enter the tip. Discard the tip and buffer.

Load Amount500 µL of the flow cell priming mix into the inlet port. Load by slowly twisting the dial in the counterclockwise direction. Wait Duration00:05:00 .

5m
Pipetting
While the priming mix is incubating, prepare the library:
AB
Reagent Volume
Sequencing Buffer (SB) 100 uL
Library Beads (LIB) 68 uL
DNA Library 32 uL
Total 200 uL
Incubation
After the 5-minute incubation, add another Amount500 µL of flow cell priming mix to the inlet port.

Pipetting
Immediately add the Amount200 µL of the library slowly into the inlet port.

Pipetting
Close the inlet port and wait for the library to incubate for Duration00:10:00 before starting any sequencing.

10m
Incubation
Flow cell wash

A flow cell wash should be done as soon as possible after the sequencing run is complete.

Wash
Place the Wash Mix (WMX) TemperatureOn ice , and thaw the Wash Diluent (DIL) at TemperatureRoom temperature .

Vortex the Wash Diluent thoroughly.

Mix
Make the Flow Cell Wash Mix by adding the following to a 1.5ml Eppendorf tube:
AB
Reagent Volume
Wash Diluent (DIL) 398 uL
Wash Mix (WMX) 2 uL
Pipette to mix and place TemperatureOn ice .

Pipetting
Mix
Stop the sequencing run on Minknow, and leave the flow cell in the port.

Make sure the inlet port is closed, and remove waste from port 2 or port 3.

Open the inlet port and set the P1000 to 200. Remove the air bubble by turning the wheel until it reaches 220-230, and a small volume of buffer enters the pipette tip.

Load Amount400 µL of the Flow Cell Wash Mix into the inlet port. Incubate for Duration01:00:00 .

1h
Incubation
Pipetting
After 1 hour, remove the waste again from ports 2 or 3. Make sure the inlet port is closed.

Remove the air bubble if it is present after removing the waste. Then add Amount500 µL of Storage Buffer (S). The flow cell can now be placed back into a Temperature4 °C refrigerator for long-term storage. Incubate the flow cell at least DurationOvernight before doing another flow cell check.

Incubation
Pipetting