Hi Rahul,
How large was your genome? How much memory was needed for your run? I received this error message at the start of Step 2:
"Could not allocate space for sequence"
Unconfigured Ad
Collapse
X
-
Dear All,
I ran Repeatscout successfully, Commands I used:
Code:1225 ##RepeatSout Run 1226 #step1 1227 build_lmer_table -l 14 -sequence Final_assembly.fasta -freq Final_assembly.freq 1228 #step2 1229 RepeatScout -sequence Final_assembly.fasta -output Final_assembly_repeats.fasta -freq Final_assembly.freq -l 14 1230 #step3 1231 cat Final_assemblyf_repeats.fasta | filter-stage-1.prl > Final_assembly_repeats_filtered_stg1.fasta 1232 #step4 1233 RepeatMasker -pa 20 -s -lib Final_assembly_repeats_filtered_stg1.fasta Final_assembly.fasta & 1234 #step5 1235 cat Final_assembly_repeats_filtered_stg1.fasta | filter-stage-2.prl --cat=Final_assembly.fasta.out --thresh=3 > Final_assembly_repeats_filtered_stg2_thresh3.fasta 1236 #step6 1237 RepeatMasker -pa 20 -s -lib Final_assembly_repeats_filtered_stg2_thresh3.fasta Final_assembly.fasta &
Leave a comment:
-
-
Thats true and it works fine, but RepeatModeler also uses RepeatMasker and eventually the rmblast package, so you might have to face the same problems as described before.
Leave a comment:
-
-
Hello,
This is not a direct answer to your question, but there is a tool from the Repeat Masker group.
Its called Repeat Modeler, this tool integrates Repeat Scout, RECON and TRF.
It creates a de-novo repeat library and then annotates the sequences.
Repeat Modeler
--
pg
Leave a comment:
-
-
I don't know if its still an actual problem, but I had it too and was able to solve it on my system (ubuntu11, 64bit).
The libs RepeatMasker is looking for are not the downloaded ones, but the blast dbs that should have been created by rmblast. rmblast itself is looking for a libpcre.so.0 file which it could not find on my system. The file is known to cause problems with some progs as symlinks are not made correctly during updates.
Therefore I just created symlinks manually in my /lib/ and /lib32/ folder to the actual file (so just type "sudo ln -s /lib/libpcre.so.3 /lib/libpcre.so.0" and "sudo ln -s /lib32/libpcre.so.3 /lib32/libpcre.so.0") and afterwards everything worked fine for me
@edge: you don't need to change anything in the .prl file, but you need to rename the trf404-linux64 (or else) executable to simply to trf.Last edited by WhatsOEver; 04-20-2012, 01:27 AM.
Leave a comment:
-
-
same thing happened to me -- the filtered output file is empty after running for a very long time. it was run on a repeat-rich genome.
could it be that i don't have nseg and TRF properly installed? there is no output about those two programs that i can see...
Leave a comment:
-
-
repeatscout
hello everyone
i m try to work with repeatscout but every time when i m runninf filter-stage-1.prl, the filtered library generated is created empty( no data)..... any solution???
Leave a comment:
-
-
Hi Zimbobo,
Can I ask you how you edit the perl script, filter-stage-1.prl to allow it point to the TRF path that we install?
Which line of filter-stage-1.prl that we need to edit the path of TRF?
My server keep on shown the below message:
"No such file or directory at ./filter-stage-1.prl line 110"
Thanks a lot for your sharing and guiding.
Leave a comment:
-
-
I actually followed those instructions.
RepeatMasker is complaining still about missing libraries (ie Libraries/RepeatMasker.lib etc) and advises to get something from www.girinst.org.
The whole point of running RepeatScout for me is to build my own library. Is there a flag to teach RepeatMasker not to look for those libraries or is there a reason RepeatMasker must have those libraries?
Leave a comment:
-
-
RepeatMasker & RepeatScout
Hello there,
I was wondering whether anybody on this list could knows how to run RepeatScout (1.0.5) and RepeatMasker (3.2.8).
Basically I have a new genome, and want to use RepeatScout to make a
library for RepeatMasker.
Here is what I do:
build_lmer_table -sequence genome.fa -freq genome.fq
RepeatScout -sequence genome.fa -output repeats.fa -freq genome.fq
filter-stage-1.prl repeats.fa &> repeats.fa.filter_1
RepeatMasker genome.fa -e abblast -lib repeats.fa.filter_1
Now:
Do I use the correct file for -lib?
RepeatMasker is still complaining about not finding Libraries/RepeatMasker.lib
and Libraries/RepeatmaskerLib.embl.
Thanks a lot in advance for any help.Tags: None
-
Latest Articles
Collapse
-
by SEQadmin2
Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
...-
Channel: Articles
06-02-2026, 10:05 AM -
-
by SEQadmin2
With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.
Introduction
Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...-
Channel: Articles
05-22-2026, 06:42 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, Today, 10:09 AM
|
0 responses
8 views
0 reactions
|
Last Post
by SEQadmin2
Today, 10:09 AM
|
||
|
Started by SEQadmin2, Yesterday, 08:59 AM
|
0 responses
14 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 08:59 AM
|
||
|
Started by SEQadmin2, 06-02-2026, 12:03 PM
|
0 responses
22 views
0 reactions
|
Last Post
by SEQadmin2
06-02-2026, 12:03 PM
|
||
|
Started by SEQadmin2, 06-02-2026, 11:40 AM
|
0 responses
19 views
0 reactions
|
Last Post
by SEQadmin2
06-02-2026, 11:40 AM
|
Leave a comment: