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Thread | Thread Starter | Forum | Replies | Last Post |
ATAC-seq primers | Fasteno | Sample Prep / Library Generation | 14 | 02-06-2020 07:06 AM |
ATAC-seq protocol | wen yuan | Sample Prep / Library Generation | 69 | 02-22-2018 09:01 AM |
ATAC-seq quality control | Kath | Bioinformatics | 1 | 09-07-2016 01:48 PM |
ATAC-seq QC using gel | Fasteno | Sample Prep / Library Generation | 0 | 03-12-2015 05:13 AM |
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#1 |
Junior Member
Location: Norway, Bergen Join Date: Nov 2016
Posts: 3
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Hello,
Could anyone please drop any comments on libraries that i have prepared using on-plate ATAC protocol (DOI: 10.1186/s13059-015-0840-9). Libraries seem to be overtagmented, but i would like to receive any comment considering their sequencibility and further actions of optimising tagmentation protocol. This time i used standard NEXTERA protocol(2,5ul of enzyme) and 50000 HeLa cells. Thanks in advance. |
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#2 |
Member
Location: UK Join Date: Jun 2012
Posts: 14
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Hi,
did you get any feedback on those libraries? I have got something similar but from different cells. Did you sequenced them at the end? if yes, how was the result? Thanks Dam |
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#3 |
Junior Member
Location: Norway, Bergen Join Date: Nov 2016
Posts: 3
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No, those libraries haven`t been sent for sequencing. Instead we have produced another samples. The thing is they are the way too overtagmented, so go down with incubation time(even to 5-10 minutes) or try removing permeabilization step.
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Tags |
atac-seq, library preparation |
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