Moderator: h.mon
h.mon ♦ 3.9k
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Posts by h.mon
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Comment:
C: Problem with SMART
... Did you `hmmpress` you HMM profile?
**edit**: in general, you should provide more details, such as command used, which HMM profile, and so forth. ...
written 4 days ago by
h.mon ♦ 3.9k
1
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105
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... You could try [MITObom][1] or [Arc][2], using your drafts as starting points.
[1]: https://github.com/chrishah/MITObim
[2]: https://ibest.github.io/ARC/ ...
written 9 days ago by
h.mon ♦ 3.9k
1
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1
answer
147
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1
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... Read ["Tutorial: How To Ask Good Questions On Technical And Scientific Forums"][1], and then elaborate a bit more your question.
[1]: https://www.biostars.org/p/75548/ ...
written 11 days ago by
h.mon ♦ 3.9k
1
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1
answer
140
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1
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Comment:
C: inversion detection in sequencing
... You probably mean Lumpy? Or is there a Lumy as well? ...
written 15 days ago by
h.mon ♦ 3.9k
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113
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... It should not make any difference for single-end data, but you can easily test: just run htseq-count with both options, one at a time.
The `--pos` argument is used to determine how paired reads are sorted on the sam/bam file, to select internally how to find read pairs. ...
written 15 days ago by
h.mon ♦ 3.9k
0
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1
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139
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1
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... What was your previous bowtie2 command? The command you posted seems pretty standard, I wonder what you were trying before. ...
written 15 days ago by
h.mon ♦ 3.9k
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65
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... Basically, you are using the wrong tool for the task you want. Try Mauve, BWA (not sure if it handles 40K long sequences, though) or even Blast.
**edit**: also, see [this][1] thread.
[1]: https://www.biostars.org/p/67632/ ...
written 15 days ago by
h.mon ♦ 3.9k
1
vote
1
answer
139
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1
answers
... I assume you have RNAseq data? Check [this][1] answer, and do the same: use BBDuk to check for rRNA contamination on your samples. You may also use SortMeRNA for this, I think it is slightly more sensitive, but a lot slower. Either way, you will know how bad your rRNA contamination was, and both pro ...
written 16 days ago by
h.mon ♦ 3.9k
1
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0
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110
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... My only suggestion at this point is for you to type all the command from the beginning (do not copy / paste), and use tab completion where appropriate to avoid errors. ...
written 16 days ago by
h.mon ♦ 3.9k
0
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1
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152
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1
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... Did you apply any quality filters to avoid spurious SNPs? And please, update your question, describing what you did in more detail. ...
written 17 days ago by
h.mon ♦ 3.9k
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For C: RCurl instalation problem
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For C: RCurl instalation problem
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For A: Script for extracting data from a tab-delimited file
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For A: RNAseq design: differential expression between sexes in several species
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