Unconfigured Ad
Collapse
X
-
these are the instructions from Readme.txt:Originally posted by ECO View PostMaybe report what errors you encountered...?
MacOSX: Copy the libtbb.dylib from ./lib into your lib searchpath.
I copied ibtbb.dylib to /usr/local/bin
but I am not able to figure out from the instructions what are the next steps after copying this file to /usr/local/bin.
I tried to run it:
far --adapters adapters.fasta --source test.fa --target test_result.fa --format fasta --log-level ALL --cut-off 4 --min-overlap 6
-bash: far: command not found
thanks
Comment
-
-
Guys, where's the OS X binary? Anyway, I'm trying to build my own TBB and FAR. Meanwhile, you should check if link path of libtbb.dylib is properly set:Originally posted by ECO View PostI can't get it to run either. Seems there are either files missing and/or it's not compiled correctly for OSX...shame, seems like a cool utility!
The first line should be the path you want it to be (i.e. /usr/local/lib). You may change it byCode:$ otool -L libtbb.dylib
In precompiled far you should change it by issuingCode:$ install_name_tool -id /usr/local/lib/libtbb.dylib libtbb.dylib
This hopefully should work (although it is hard to guess without the error you get).Code:$ install_name_tool -change /path/to/libtbb.dylib /usr/local/lib/libtbb.dylib far
@joseph: your far installation should be in a directory in the PATH env variable :-)
Comment
-
-
I tried to install dawe's precompiled binary (Thanks for sharing!!!). It is for OSX correct?
I ran:
Then I made a couple short test files if fasta format because it is the most simple.Code:sudo tar xvzf far.tgz -C /usr/local
And this is what I get:
Not sure what a segmentation fault is, but could it be that the precompiled binary dawe posted isn't exactly right for my computer?Code:$ far -s fartest.fasta -t fartestout.fa -f fasta -a IlluminaAdapters.fa source file was set to fartest.fasta. No 2nd input file specified! (Run is not paired) target file was set to fartestout.fa. File format was set to FASTA Will do demultiplexing and adapter removal... Adapter file: IlluminaAdapters.fa Nr. of allowed indels + mismatches per 10 bases: 2 Allowed number of uncalled bases was set to 0 Chosen scoring scheme: match = 3 ,mismatch = -3 ,gap opening = -20 Trimming from right end. Minimum required overlap: 10 Overlap will be treated as standard overlap. Segmentation fault
--------------
Ethan
Comment
-
-
Hi Ethan
it worked fine for me
these are the files:Code:far --source myfile.fastq --target myoutput.fastq --format fastq --adapters adapters.fasta --nr-threads 4 far --source SRR309288.fastq --target SRR309288_far_trim --format fastq --adapters adapter.fa --nr-threads 2 source file was set to SRR309288.fastq. No 2nd input file specified! (Run is not paired) target file was set to SRR309288_far_trim. File format was set to FASTQ-illumina15 Will do demultiplexing and adapter removal... Adapter file: adapter.fa Nr. of allowed indels + mismatches per 10 bases: 2 Allowed number of uncalled bases was set to 0 Chosen scoring scheme: match = 3 ,mismatch = -3 ,gap opening = -20 Trimming from right end. Minimum required overlap: 10 Overlap will be treated as standard overlap. Adapter sequences are: adapter TCGTATGCCGTCTTCTGCTTGT No barcodes file specified... Minimum required readlength: 18 Using 2 threads. Writing omitted read ids to: SRR309288.fastq.omitted Using no phred-quality trimming. Starting processing (algorithm: needleman-wunsch)... Done. Calculation Time: 28 minutes 53 seconds. Step 1 - filtering input files: =============================== Input file contained 13823407 reads. Discarded in total 309069 reads due to containing uncalled bases. Discarded in total 0 reads due to having low quality. Used 13823407 reads from input file. 12037203 reads remaining ( 85.1741 % of input reads ) Statistics on each output file: =============================== File: SRR309288_far_trim.fastq Nr. of reads dropped due to being shorter than minLength: 1477135 Nr. of reads written to the file: 12037203 Writing length distributions of reads (for each file) Statistics on adapter removal (input files): ============================================ Adapter removal_count adapter 10847050 Min-/Max-/Mean-/Median-overlap length: 10 / 23 / 12 / 11
Code:> head -20 SRR309288.fastq @SRR309288.1 ILLUMINA-432AEC_0016:4:1:959:1667 length=36 NNNNNNNNCNNNNTNATGTTGACATCTCGTATGCCG +SRR309288.1 ILLUMINA-432AEC_0016:4:1:959:1667 length=36 #################################### @SRR309288.2 ILLUMINA-432AEC_0016:4:1:959:8156 length=36 NNNNNNNNCNNNNNNTATGCCGTCTTCGGCTTGCAA +SRR309288.2 ILLUMINA-432AEC_0016:4:1:959:8156 length=36 #################################### @SRR309288.3 ILLUMINA-432AEC_0016:4:1:959:1631 length=36 NNNNNNNNCNNNNTNATGTTGACATCTCGTATGCCG +SRR309288.3 ILLUMINA-432AEC_0016:4:1:959:1631 length=36 #################################### @SRR309288.4 ILLUMINA-432AEC_0016:4:1:960:2745 length=36 NNNNNNNNCNNANANCATCTCGTATGCCGTCTTCTG +SRR309288.4 ILLUMINA-432AEC_0016:4:1:960:2745 length=36 ########(##'#1#4366.???>><>?>???>?>7 @SRR309288.5 ILLUMINA-432AEC_0016:4:1:960:1472 length=36 NNNNNNNNTNNANTNAGAAGGCATCTCGTATGCCGT +SRR309288.5 ILLUMINA-432AEC_0016:4:1:960:1472 length=36 #################################### > head -20 SRR309288_far_trim head: SRR309288_far_trim: No such file or directory boyce-162-119:FAR jdhahbi$ head -20 SRR309288_far_trim.fastq @SRR309288.531 ILLUMINA-432AEC_0016:4:1:1019:15214 length=36 CACCCGTAGAACCGACCTTGCATC + GFEGGFFAFDAECDCFFFDFEEGE @SRR309288.532 ILLUMINA-432AEC_0016:4:1:1019:12253 length=36 CTGAGCCGAGAATGGGGATC + FF5FFFDFEDBADDD-DCAD @SRR309288.533 ILLUMINA-432AEC_0016:4:1:1019:9688 length=36 GCATTGTGGTTCAGTGGTAGAATTCTCGATCTCGTA + :E?EEAEEEEBE?D?EEA?ED=DEE5EE-:DD-DDA @SRR309288.534 ILLUMINA-432AEC_0016:4:1:1019:6554 length=36 TAGCTTATCAGACTGATGTTGACATC + FGGGGGGFGDEGGGGGGGGGFGGGGG @SRR309288.535 ILLUMINA-432AEC_0016:4:1:1019:15771 length=36 TAGCTTATCAGACTGATGTTGACATC + GFGFFFA?DFE-BEDBFDFFF?F:EF
Comment
-
-
@All,
are you happy with FAR or are you using other tools for (illumina) adpator/quality clipping?
I am trying to figure out which is the "best" one, in terms of flexibility and good results.
Currently I am playing around with far (surely developed for Mac as the Makefile needs to be fixed for compiling on linux). It seems quite flexible, "verbose" and it works on PE data directly.
Sven
Comment
-
Latest Articles
Collapse
-
by SEQadmin2
Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
...-
Channel: Articles
07-09-2026, 11:10 AM -
-
by SEQadmin2
Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.
There is no single reason why many patients don’t respond to treatment as expected. Cancer is...-
Channel: Articles
07-08-2026, 05:17 AM -
-
by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
-
Channel: Articles
07-01-2026, 11:43 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 07-13-2026, 10:26 AM
|
0 responses
24 views
0 reactions
|
Last Post
by SEQadmin2
07-13-2026, 10:26 AM
|
||
|
Started by SEQadmin2, 07-09-2026, 10:04 AM
|
0 responses
34 views
0 reactions
|
Last Post
by SEQadmin2
07-09-2026, 10:04 AM
|
||
|
Started by SEQadmin2, 07-08-2026, 10:08 AM
|
0 responses
21 views
0 reactions
|
Last Post
by SEQadmin2
07-08-2026, 10:08 AM
|
||
|
Started by SEQadmin2, 07-07-2026, 11:05 AM
|
0 responses
34 views
0 reactions
|
Last Post
by SEQadmin2
07-07-2026, 11:05 AM
|
Comment