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Building a better pangenome #306
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Hi @George-du, there are several possibilities:
I would recommend the first option, though I am aware of the computational overhead. |
Thank you for your reply, I will take your suggestion and feel that adding the new function of PGGB to add new samples will be very helpful and useful. |
A future option would be to only generate alignments that would be induced
by the addition of the new samples. This would be helpful because most of
the runtime is dependent upon the quadratic, all2all alignment.
…On Tue, Jun 20, 2023, 05:23 George-du ***@***.***> wrote:
Thank you for your reply, I will take your suggestion and feel that adding
the new function of *PGGB* to add new samples will be very helpful and
useful.
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Sounds great, thanks so much for your help. |
Hi, I'm curious if I described the problem clearly and if there are some suggestions about the solution to this problem? |
Hi, developers! |
Hi, @subwaystation @ekg , I tried the above strategy on human chromosome 13, but the smoothxg step is still giving errors at the moment. Are there any some suggestions about this problem or can I just use the results before the smoothxg step?
the command: the error message:
the command: the error message: I'm looking forward to your reply. |
Can you try the same command lines, but installing PGGB via Docker/Singularity? |
Hi, developers! I will try to install PGGB via Docker/Singularity, Do I need to install a specific version? |
The latest version available, thanks! |
Got that. I'll try it again. |
Hi, @subwaystation @ekg @AndreaGuarracino, I installed the latest PGGB (pggb 8eaf354) using Singularity with non-root privileges, but still get a similar error. The details of the reported error are as follows: 1.re-run the smoothxg program without the -Q Consensus_ parameter and the -O 0:(mash length: 50kb/10kb) the command:10kb 50kb the error message:10kb 50kb 2. re-run the PGGB pipeline using Singularity: the command:RUN_PGGB="singularity exec /home/Software/pggb/pggb.simg pggb" the error message:[wfmash::skch::Map::mapQuery] count of mapped reads = 13369, reads qualified for mapping = 13641, total input reads = 13641, total input bp = 24623027601 Do you have any suggestions for these reported errors? Thanks! I'm looking forward to your reply. |
It looks like two different issues. If you re run do you ever get the exact same error in smooth and lace? |
@ekg @subwaystation @AndreaGuarracino Hi, developers! The second attempt is the result of running the PGGB process completely from scratch using the Singularity image (non-root install), which produces an error after the wfmash step , so it could not run to the smoothxg step. The first attempt was based on the output of the Linux installation version (the smoothxg step was incorrect), and then this step was re-executed using the smoothxg software in Singularity Images. It really is two different issue. Thanks in advance! |
Hi @George-du, |
Dear @subwaystation @AndreaGuarracino, Here is the raw data I used for the above pipeline, please help me check the exact errors. Thanks! |
Dear @subwaystation @AndreaGuarracino,
Here is the raw data I used in the above pipeline, please help me check the exact error. Thanks!
(https://sandbox.zenodo.org/record/1234413)
At 2023-08-17 20:58:03, "Simon Heumos" ***@***.***> wrote:
Hi @George-du,
would it be possible to share your input data or a tiny subset of it, which produces the issues? Thanks!
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Dear @subwaystation @AndreaGuarracino, Can the data be downloaded and used properly? |
@George-du, thank you for the data. I am running
It is taking a while. At the moment it is at the 2nd round of SPOA, without issues. |
Dear @AndreaGuarracino @subwaystation, Wow, that sounds good. The version of the software I'm using in the PGGB pipeline is as follows. Additionally, I found that some of the chromosome Smoothxg steps were taking an extraordinarily long time to run and ended up generating errors (chr15 ; ~1 month ; Command terminated by signal 7 ) . The detail is as follows: The software version of PGGB pipeline: The commands and results are as follows (chr15 ; ~1 month ; Command terminated by signal 7) : Looking forward to the resolution of this issue. Thanks in advance. |
Is there a possibility for you @George-du to run our latest Docker image? |
Dear @subwaystation, I will contact the administrator and try to run the latest Docker image. Thanks. |
@George-du, I was able to finish PGGB. It seems the problem is specific to your installation and/or cluster. I've used general:
input-fasta: /lizardfs/guarracino/bug_smoothxg/chr13.pan.new.fa.gz
output-dir: /lizardfs/guarracino/bug_smoothxg/xxx
temp-dir: /scratch
resume: false
compress: false
threads: 48
poa_threads: 48
wfmash:
version: v0.10.4-7-g0981b92
segment-length: 50000
block-length: 250000
map-pct-id: 98
n-mappings: 236
no-splits: false
sparse-map: false
mash-kmer: 19
mash-kmer-thres: 0.001
exclude-delim: false
no-merge-segments: false
seqwish:
version: v0.7.9-2-gf44b402
min-match-len: 311
sparse-factor: 0
transclose-batch: 10000000
smoothxg:
version: v0.7.0-18-g4ff4cf2
skip-normalization: false
n-haps: 236
path-jump-max: 0
edge-jump-max: 0
poa-length-target: 700,900,1100
poa-params: 1,19,39,3,81,1
poa_padding: 0.001
run_abpoa: false
run_global_poa: false
pad-max-depth: 100
write-maf: false
consensus-spec: false
consensus-prefix: Consensus_
block-id-min: .9800
block-ratio-min: 0
odgi:
version: v0.8.3-26-gbc7742ed
viz: true
layout: true
stats: false
gfaffix:
version: v0.1.5
reduce-redundancy: true
vg:
version: v1.50.1
deconstruct: false |
Wow, I'll reinstall the latest version of PGGB and test it out. |
Hi, How to add new sample genomes and contigs to an existing pan-genome producted by PGGB, and whether it can be done directly using the Minigraph or GraphAligner tool. Any suggestions on how to do this.
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