Question: How can I assembly big genome by abyss with 128 Gb ram
gravatar for Mbillah
13 days ago by
Mbillah100 wrote:

I tried to get 140 million read assembly by abyss-pe, But memory could not load it(sparsehash fatal error). As a result I divided my fastq file and created two contig file (70 million reads). is there any quality problem? and now I want to make this contig file one. how can I do this? Can I continue to work with the combined contig file?

assembly • 139 views
ADD COMMENTlink modified 13 days ago by jean.elbers450 • written 13 days ago by Mbillah100

I wouldn't divide up the fastq.

Soapdenovo2 might be more memory efficient for you.

Minia certainly will be, but assemblies are poor in my experience.

Good luck.

If you're really struggling and those tools don't work I could perhaps run assemblies for you if you gave me the exact commands to run.

ADD REPLYlink written 12 days ago by colindaven830

Although Minia alone really produces too fragmented assemblies, the GATB-Minia-Pipeline results in better assemblies and keep memory usage low.

ADD REPLYlink written 12 days ago by h.mon21k
gravatar for jean.elbers
13 days ago by
jean.elbers450 wrote:

ABySS offers a bloom filter (, so you could redo the assembly using the bloom filter to reduce memory usage.

ADD COMMENTlink written 13 days ago by jean.elbers450
Please log in to add an answer.


Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1469 users visited in the last hour