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. Author manuscript; available in PMC: 2024 Apr 29.
Published in final edited form as: Nat Protoc. 2021 Oct 18;16(12):5377–5397. doi: 10.1038/s41596-021-00608-z

Table 2.

Troubleshooting table.

Step Problem Possible reasons Solutions
14 No nuclei pellet Spin conditions Extend spin time or speed
38 Loss of nucleosomal banding Chromatin integrity disrupted during cell collection Try alternative methods of cell dissociation during collection to maintain high viability
Over-tagmentation Scale down reaction size relative to cell number or increase the starting number of cells
Decrease transposition incubation time
Accumulation of large size fragments Under-tagmentation Reduce cell numbers or scale up reaction size relative to cell number
Increase transposition incubation time
69 Low yield Insufficient lysis Additional pipetting following addition of lysis buffer
Inaccurate cell count Repeat cell counting, confirming single cell suspension has been achieved and viability is high (>80%)