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Old 01-14-2013, 11:25 AM   #1
Location: NYC

Join Date: Jun 2010
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Default Plasmid library sequencing-which platform (if any)?

Hi everyone

I was hoping to pick your brains for a second. We have a plasmid library in e coli. We would like to obtain sequences form hundred of individual plasmids, starting from the backbone (meaning from an arbitrary primer) into the inserts.

The classical way to do this is miniprep and sanger sequencing of individual colonies. At the numbers that we would like to do, the price goes well into NGS territory.

I've been trying to find an NGS platform that would provide similar information from a plasmid prep of pooled colonies. But all the methods I've seen involve library prep and introducing an adapter that will serve as the primer for sequencing. Simple shotgun sequencing (by illumina for instance) of such a sample would give us the information, but only <5% of the reads would be informative (the rest would be backbone).

I just know that I haven't looked at all the miriad methods that have been developed. Is there a technology that will give you sequence from an arbitrary primer? Around 400bp would be great, but we could live with less.

Thanks in advance!
zaratieg is offline   Reply With Quote
Old 01-14-2013, 11:33 AM   #2
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How big are your inserts? Because even if <5% of reads were informative, that may be enough. A single lane on a HiSeq gives well over 100 million reads anymore, so if only 5% of reads are informative, that is still several million informative reads. Even if you have a couple hundred plasmids, you will have tens of thousands of 100 bp reads covering that.
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Old 01-14-2013, 03:04 PM   #3
Location: NYC

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Thank you Chadn, that's what I was figuring. I was wondering if there was a more elegant/less brute force approach, but i guess that we are at a point where it really is economical to kill flies with a 155 howitzer.
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Old 01-15-2013, 10:52 AM   #4
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Location: Purdue University, West Lafayette, Indiana

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You could just pool the plasmids and amplify the inserts using vector primers, then create libraries from the amplified DNA.

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Old 01-22-2013, 12:01 PM   #5
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As another poster mentioned, PCR amplify your insert, if you really want to avoid backbone. You can even put Illumina adaptors at the ends of your PCR primers, so you don't have to do any kind of library prep.
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