Paired-End Read Trimming with Trimmomatic | Paired End Reads | Single Sample

Поделиться
HTML-код
  • Опубликовано: 1 окт 2024

Комментарии • 6

  • @vetlove4056
    @vetlove4056 3 месяца назад

    I am not getting equal reads in output fastq files how to do this I'm totally confused please guide mee please i beg

  • @DrSmoothPuller
    @DrSmoothPuller 5 месяцев назад

    i followed exactly the same steps, I saw some differences, first, after I click enter when i type in nano trim_reads.sh, it won't create additional terminal window as you did, you have two tabs in parallel, while i only have one. sec, i need to use Ctr+O instead of Ctr+S to save sh file, after the saving, it won;t to back to the original nano trim_reads.sh terminal window, i need to create a new terminal window and use chmod +x trim_reads.sh and ./trim_reads.sh, after that summary part crushed, saying A fatal error has been detected by the Java Runtime Environment:
    #
    # SIGSEGV (0xb) at pc=0x000000010c9d7648, pid=10860, tid=10243, what does this mean? thank you for help

    • @bioinformaticscoach
      @bioinformaticscoach  5 месяцев назад

      Perhaps you can book a session so that we discuss more on the issue.

  • @relvant3026
    @relvant3026 Год назад

    I don't understand why did not perform fastqc in the first place

  • @kahlonmultiinsights2023
    @kahlonmultiinsights2023 Год назад

    Thanks, please provide the bash codes in free

  • @kahlonmultiinsights2023
    @kahlonmultiinsights2023 Год назад

    Is it necessary to creat trimmed_unpaired?