Question: Hybrid assembly of PacBio and Illumina reads
1
gravatar for int11ap1
4.1 years ago by
int11ap1420
Barcelona
int11ap1420 wrote:

I have a ~30X PacBio dataset and ~40X Illumina dataset, besides of a mate-pair dataset. I am trying to assemble them (the expected genome size is around ~230Mb, it's a plant) in a server with 160Gb of RAM. However, I am having problems with ALLPATHS (lack of memory at the step of CorrectLongReads).

  • Is that possible to assemble my data in a cluster with 160Gb of RAM?

  • Is that possible with ALLPATHS?

pacbio illumina • 3.5k views
ADD COMMENTlink modified 4.0 years ago by Josué Barrera10 • written 4.1 years ago by int11ap1420
2
gravatar for genomax
4.1 years ago by
genomax89k
United States
genomax89k wrote:

Have you seen this wiki page from PacBio?

As for the first question you have already answered that. There is no substitute for RAM. If the server does not have enough then finding alternate hardware may be the only option.

ADD COMMENTlink modified 4.1 years ago • written 4.1 years ago by genomax89k
1
gravatar for Josué Barrera
4.0 years ago by
Mexico
Josué Barrera10 wrote:

Given the ammount of Illumina and PacBio data you have, I would suggest a hybrid assembly using DBG2OLC. It gave me good results with 100x Illumina + 30x PacBio data, and it is memory efficient, so you could probably run it in your 160Gb RAM cluster. I would then use a scaffolding step using your mate-pair data to improve the assembly obtained from DBG2OLC and a final base correction using Pilon.

ADD COMMENTlink written 4.0 years ago by Josué Barrera10

How would you use mate-pairs reads after DBG2OLC?

ADD REPLYlink written 2.3 years ago by Ric300
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