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#1 |
Junior Member
Location: Madison, WI, USA Join Date: Jan 2011
Posts: 6
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Hi all,
I am working on a mammalian genome project. We have an assembly from PacBio reads with N50 = 6.2 Mb. We would like to generate some long-range data that could be used for scaffolding. I am aware of several options, including Nanopore, Hi-C (with Dovetail or Phase Genomics), optical maps (Bionano), and synthetic long reads (10X). Can you share your experiences with these technologies? We need help choosing which one(s) to use. Thanks. Yury |
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#2 |
Jafar Jabbari
Location: Melbourne Join Date: Jan 2013
Posts: 1,230
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You already have a good N50 with long reads. The options are combination of 10x Link reads, Hi-C and optical mapping. Searching " Vertebrate Genomes Project Plans to Combine Technologies for 'Near Gapless' Assemblies" should give more ideas but you might be asked to create an account to access it.
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#3 |
Junior Member
Location: Madison, WI, USA Join Date: Jan 2011
Posts: 6
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Thanks for the tip, nucacidhunter!
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#4 |
Junior Member
Location: USA, NC Join Date: Apr 2019
Posts: 6
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As nucacidhunter mentioned, I would highly recommend you work with the VGP group. I've work with the VGP and had excellent results for my de novo projects. They even do the hybrid assemblies!
If your budget is tight, I would add HiC data from Phase Genomics or Arima Genomics. If phasing information is important, then add some 10X Genomics data (https://www.10xgenomics.com/solutions/assembly/). |
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Tags |
10x, hi-c, nanopore, optical mapping, scaffolding |
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