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  • SDPA_Pet
    replied
    Originally posted by flxlex View Post
    The page you mention contains the default settings, yes. Unfortunately, you can't get these from the log files.

    However, I agree with @maubp that the reviewer's request is nonsensical. What is the point of describing parameters if you don't change them? Newbler has a few dozen parameters, if you really want to spend a lot of time, see section 4.1 in the same PDF.
    Thanks. I know it's nonsense. So, if I don't want to give them these default settings, how should I reply them? You know, you are supposed to answer all the reviewers concerns.

    Leave a comment:


  • flxlex
    replied
    The page you mention contains the default settings, yes. Unfortunately, you can't get these from the log files.

    However, I agree with @maubp that the reviewer's request is nonsensical. What is the point of describing parameters if you don't change them? Newbler has a few dozen parameters, if you really want to spend a lot of time, see section 4.1 in the same PDF.

    Leave a comment:


  • SDPA_Pet
    replied
    Originally posted by GenoMax View Post
    @SDPA_Pet: Even though you used the GUI, newbler probably wrote a log file somewhere of what was happening. Find and look through that file to see if you can get the command line/options the program used.
    I am using Newbler 2.6. Can you check the link that I paste. Is the table on Page 28 listing the default settings?

    Leave a comment:


  • GenoMax
    replied
    @SDPA_Pet: Even though you used the GUI, newbler probably wrote a log file somewhere of what was happening. Find and look through that file to see if you can get the command line/options the program used.

    Leave a comment:


  • maubp
    replied
    Originally posted by [email protected] View Post
    Hi,can anyone tell me how i can convert any fastq to BAM ?

    Thanks
    rinku
    That has nothing to do with this thread about Newbler default settings. Please search the forum - this is probably a read mapping question.

    Leave a comment:


  • rinku.y8448@gmail.com
    replied
    Hi,can anyone tell me how i can convert any fastq to BAM ?

    Thanks
    rinku

    Leave a comment:


  • maubp
    replied
    As long as you list the full version number, I agree "default parameters" ought to be enough.

    (The reasoning being defaults and settings do change, so without the version number you can't infer the settings - moreover without the version number you would struggle to get the same results even if the settings hadn't changed).

    If this was at the command line, you could give the actual command in your supplementary materials to appease the reviewers.

    Leave a comment:


  • SDPA_Pet
    replied
    Well, I was using GUI version.

    Leave a comment:


  • Brian Bushnell
    replied
    Why don't you just list the version you used and the command line?

    Leave a comment:


  • Bukowski
    replied
    If you run Newbler at the command line it will probably spit out a help screen, and the default values, most command line tools will do this.

    Leave a comment:


  • SDPA_Pet
    replied
    I find their manual and a table on page 28. I was wondering if this is the default settings.

    Here is manual link



    Please help me and see if the table on Page 28 is the assemble default settings.

    thanks.

    Leave a comment:


  • SDPA_Pet
    replied
    Newbler default settings? -- Any papers

    Hi, I assembled my 454 metagenomic seqs with Newbler default setting. In my manuscripts, I wrote "assembled using Newbler with default settings. The reviewers asked me to list some details. I search a lot of papers. They all write same as me assembled with Newbler with default settings.

    Can anyone find a paper for me with using 454 metagemonics sequencings and list some details with default setting. It doesn't have to be really detailed info.

    Thanks,
    Ben

    Leave a comment:


  • SDPA_Pet
    started a topic Newbler default settings? -- Any papers

    Newbler default settings? -- Any papers

    Hi, I assembled my 454 metagenomic seqs with Newbler default setting. In my manuscripts, I wrote "assembled using Newbler with default settings. The reviewers asked me to list some details. I search a lot of papers. They all write same as me assembled with Newbler with default settings.

    Can anyone find a paper for me with using 454 metagemonics sequencings and list some details with default setting. It doesn't have to be really detailed info.

    Thanks,
    Ben

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