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Question: How to use ALLPATH-LG assembler
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Hi all the community, I actually need your help because it is the first time I have to assemble a genome.

I actually have in my possession 2 fasta file: reads1.fq and reads2.fq Those file are comming from an illumina Hiseq 3000 150bp and the genome size of my specie is around 1.5 GB.

I would like to use the programm ALLPATH-LG to do so. I read the manual before posting my question here but I still do not know what to really do. Sould I first prepare my data or is there only one commande to execute with my two fasta file and the program runs alone?

If someone could explain me more the detail the process or if someone had already used this program if he can explain me the steps of the process it would be very kind of you.

ADD COMMENTlink 20 months ago Darill • 30 • updated 20 months ago Beuss • 110
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Take a look to DISCOVAR denovo and MaSuRCA :

ADD REPLYlink 20 months ago
• 110
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Hi, thanks for you help. I'm trying to use masurca, can you tell me if my config file is correclty written please?

#PBS -S /bin/bash
#PBS -l nodes=1:ppn=8:bigmem,mem=100gb
#PBS -e /pandata/ACG-0006_0027/LOGS/ACG-006_assembly.error
#PBS -o /pandata/ACG-0006_0027/LOGS/ACG-006_assembly.out
#PBS -N ACG-006
#PBS -q q1week

PE= pe 150 22  /pandata/ACG-0006_0027/reads1.fq  /pandata/ACG-0006_0027/reads2.fq


#set this to 1 if your Illumina jumping library reads are shorter than 100bp
#this is k-mer size for deBruijn graph values between 25 and 127 are supported, auto will compute the optimal size based on the read data and GC content
#set this to 1 for all Illumina-only assemblies
#set this to 1 if you have less than 20x long reads (454, Sanger, Pacbio) and less than 50x CLONE coverage by Illumina, Sanger or 454 mate pairs
#otherwise keep at 0
#specifies whether to run mega-reads correction on the grid
#specifies queue to use when running on the grid MANDATORY
#batch size in the amount of long read sequence for each batch on the grid
#coverage by the longest Long reads to use
#this parameter is useful if you have too many Illumina jumping library mates. Typically set it to 60 for bacteria and 300 for the other organisms 
#these are the additional parameters to Celera Assembler.  do not worry about performance, number or processors or batch sizes -- these are computed automatically. 
#set cgwErrorRate=0.25 for bacteria and 0.1<=cgwErrorRate<=0.15 for other organisms.
CA_PARAMETERS =  cgwErrorRate=0.15
#minimum count k-mers used in error correction 1 means all k-mers are used.  one can increase to 2 if Illumina coverage >100
#whether to attempt to close gaps in scaffolds with Illumina data
#auto-detected number of cpus to use
#this is mandatory jellyfish hash size -- a safe value is estimated_genome_size*estimated_coverage
JF_SIZE = 200000000
#set this to 1 to use SOAPdenovo contigging/scaffolding module.  Assembly will be worse but will run faster. Useful for very large (>5Gbp) genomes from Illumina-only data

Thanks again for your help

ADD REPLYlink 20 months ago
• 30
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If this is all the data you have, you can't use Allpaths-LG, because it does requires at least two different libraries (generally one paired-end, and a second mate-pairs):

B1. Can I assemble data from ONE library using ALLPATHS-LG?

No, but we understand the need for programs that can do this, and there are some, including Velvet and ABySS. Multiple libraries enable higher assembly quality but entail more labwork.

I remember someone (maybe Brian Bushnell) posting here at BioStars about creating a "fake" mate-pairs or long reads library to be able to use Allpaths-LG with just one library.

edit: here, I found the post:

Assembler for large genome de novo assembly with Illumina paired end reads of 150 pb

ADD COMMENTlink 20 months ago h.mon 25k
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Thanks for your answer. Do you have another program to advice? I already used IDBA-UD but it is not working for this data I do not know why...

ADD REPLYlink 20 months ago
• 30

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