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  • solaymane
    replied
    hello i am new member beginner to the field

    Leave a comment:


  • RogerH
    replied
    I recently used fastx_trimmer on my data and I can only recommend it.

    Leave a comment:


  • dgtnk
    replied
    perl is OK
    fastx_trimmer provided by FASTX_Toolkit may be faster.

    Leave a comment:


  • empyrean
    replied
    i use perl.. keep the right end.. and trim the left end.. i already trimmed adapters..

    Leave a comment:


  • maubp
    replied
    Do you mean keep the left end, or keep the right end?

    What is your favourite scripting language (since there are lots of options here, Perl, Python, Ruby, etc)?

    Leave a comment:


  • empyrean
    started a topic Cut the reads.. paired end fastq file

    Cut the reads.. paired end fastq file

    hi.. i have the following 150bp reads.. i would like to cut the bases which are more than 100bp. Also i would like to cut from begining of the read. please let me know any script or program which can do this.

    Code:
    @HWI-DO4456:7:000000000-Z07CL:1:1:15052:1479 1:N:0:GGCTAC
    TCCTCAGATTTTTTAGAAAGAGGAGTCTGCTTATAAGATAATGGCATCATTTTGATAGAATCTCCTCGCATTGTTGTAAAACTAATAACAAAGAAGGTTGGTTTTTGTGGTTTTGGTCTCCCGGCCTGAATCCAAGCTTGATGAATACGAA
    +
    @CCFFFFFHHHHHJJIJJJJJJIJJJJJJJJJIJJJIJJJIJJJJJJJJJJJJIJJJJJJIJGJJJJJJFHHFFFFFEEEEDEDDDDDDDCDDCBDD>@CB?BDDDDDDDCBDDDBBCDDDDDDDBDDDDDDDDDCBCDCBCDDDDEDDDD
    @HWI-D04456:7:000000000-Z07CL:1:1:17590:1511 1:N:0:GGCTAC
    TTAATTATACTTGTTGGTTTTGGTGGCGGATTAACATGGGGAGCAGTCGCTCTTCGTTGGGGTAAATAAGGACTGAGAGAAAAAAAGGAGTGTATTTTGTGAAGGTAGGGGCACAGTACCGTTGAAGCGTCTAATGAACGTGGAGGGATGG
    +

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  • seqadmin
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