Comments (8)
I have just tried the following: copy the binary from m1 to m2, and run the
m1's fastq-mcf on m2: it works. Something specific to m2 happens during the
compilation (gcc does not produce any error message during the compilation of
fastq-mcf).
Original comment by [email protected]
on 25 Mar 2013 at 10:21
from ea-utils.
Also, version ea-utils.1.1.2-484 does not have this problem on m2
Original comment by [email protected]
on 25 Mar 2013 at 10:54
from ea-utils.
is it possible for you to post the adapters files and at least a subset of the
fastq's with the incorrect behavior? i'm running those same Ubuntu gcc version
on several boxes.
Original comment by [email protected]
on 28 May 2013 at 5:11
from ea-utils.
Have you tried just getting the "latest version"? r600+ ?
Original comment by [email protected]
on 3 Jun 2013 at 1:23
from ea-utils.
Hi,
I just tested the latest SVN version, and using the same example got:
zgrep -c AAGCAGTGGTATCAACGCAGAGTACTTTTT test1.fastq.gz
817
(expected is 0, and raw data gives: 92403)
So that's much better. I still wonder why ~800 out of the 92403 adapters still
find their way to the output...
My adapter file is the following:
>MINTadapterFiveprime
AAGCAGTGGTATCAACGCAGAGTACGGGGG
>MINTadapterThreeprimeA
AAGCAGTGGTATCAACGCAGAGTACTTTTT
>PE1adapter
AGATCGGAAGAGCGGTTCAGCAGGAATGCCGAG
>PE2adapter
ACACTCTTTCCCTACACGACGCTCTTCCGATCT
>PE1PCRprimer
AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT
>PE2PCRprimer
CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT
>Illumina_Multiplexing_PCR_Primer_2.01
GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT
>C_Illumina_Multiplexing_PCR_Primer_2.01
AGATCGGAAGAGCACACGTCTGAACTCCAGTC
>adapThreep_TAGATG
AGATCGGAAGAGCACACGTCTGAACTCCAGTCACTAGATGATCTCGTATGCCGTCTTCTGCTTG
>adapThreep_CTTGTA
AGATCGGAAGAGCACACGTCTGAACTCCAGTCACCTTGTAATCTCGTATGCCGTCTTCTGCTTG
>adapThreep_GGCTAC
AGATCGGAAGAGCACACGTCTGAACTCCAGTCACGGCTACATCTCGTATGCCGTCTTCTGCTTG
>adapThreep_ATCACG
AGATCGGAAGAGCACACGTCTGAACTCCAGTCACATCACGATCTCGTATGCCGTCTTCTGCTTG
>Mint2-Threep-CDS-4M adapter
AAGCAGTGGTATCAACGCAGAGTGGCCGAGGCGGCCTTTTGTTTTTTCTTTTTTTTTTTTT
>C_adapFivep
AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCGTATCATT
>C_MINT2-Fivep-PlugOligo-3M-adapter
CCCCCGGCCGTAATGGCCACTCTGCGTTGATACCACTGCTT
>C_MINT2-Fivep-PlugOligo-1-adapter
CCCGCGTACTCTGCGTTGATACCACTGCTT
>C_MINT1adapterFiveprime
CCCCCGTACTCTGCGTTGATACCACTGCT
Best,
Original comment by [email protected]
on 3 Jun 2013 at 2:29
from ea-utils.
i'm guessing that those adapters are either a) not at the end or b) masked by
too much mismatch?
Original comment by [email protected]
on 3 Jun 2013 at 5:47
from ea-utils.
... but that's just a guess. i'd need to see the stderr output as well, and
would really like to be able to run in a debug mode on the original file, and
try to isolate the reads that are an issue, etc.
Original comment by [email protected]
on 3 Jun 2013 at 5:50
from ea-utils.
Can't reproduce. No resp in 2 months, closing.
Original comment by [email protected]
on 12 Aug 2013 at 1:24
- Changed state: WontFix
from ea-utils.
Related Issues (20)
- sam-stats fails to properly deduce unmapped reads and snp (ins/del) rate HOT 6
- --max-ns 0 does not seem to work, still getting reads with Ns HOT 6
- Add "make clean" target to Makefile HOT 3
- fastq-mcf: Allow merging multiple FASTQ input files to one (or two in case of paired-end) cleaned fastq file HOT 4
- sam-stats doesn't support -o and -O option HOT 3
- Incorrect total reads when using FIFO HOT 2
- fastq-mcf: invalid adapter file ==> Floating point exception HOT 1
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- fastq-multx when barcode is in header between # and / symbols? HOT 7
- fastq-multx supporting sequence in header HOT 1
- Compilation on Mac HOT 1
- Giant FASTQ support in stats HOT 3
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- fastq-mcf not working correctly on ubuntu 14.04 HOT 9
- error message: "fastq-mcf has stopped working" HOT 4
- gtf2bed wrong output. HOT 1
- compilation error because sparsehash/sparse_hash_map is not found HOT 1
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