A step-by-step guide to ChIP-seq data analysis

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  • Опубліковано 27 січ 2025

КОМЕНТАРІ •

  • @ManchesterBCF
    @ManchesterBCF 9 років тому +12

    A very clear and informative tutorial. Just to add that the latest version of the peak caller (MACS2) specifically handles paired-end mapped reads. This results in a more accurate estimation of the mean DNA fragment size that can lead to a better estimation of the peak summit.

  • @ziqifu2232
    @ziqifu2232 3 роки тому

    Extremely helpful and detailed introduction to sequencing! Thank you.

  • @peipeiguo3169
    @peipeiguo3169 6 років тому +1

    thank you for this great presentation!
    Very clear, practical and informative.

  • @thirupugal
    @thirupugal 6 років тому +2

    Very informative, thank you

  • @susanhsiao7867
    @susanhsiao7867 6 років тому +1

    Thank you. It is exactly what I need.

  • @elviskim9806
    @elviskim9806 6 років тому +1

    amazing tutorial

  • @MAISARAHABSAMAD
    @MAISARAHABSAMAD 7 років тому +1

    Thank you so much for this tutorial

  • @cathytang2558
    @cathytang2558 4 роки тому +1

    Thanks, explain the overall workflow very well. Just wondering if anyone has any recommendations about a tutorial that explains everything in terms of the command-line/ programming environment so that we can plot whatever we want.

    • @TheRookieAnalyst
      @TheRookieAnalyst 4 роки тому +1

      You can try making use of the Biostar Handbook_2nd edition by Dr. Istvan Albert. It contains practical guide into the command line/programing environment using different OS as case study. All the best.

  • @sunnyyoda5511
    @sunnyyoda5511 6 років тому +1

    THANK YOU, Thank You, Thank you, thank you

  • @patriziopanelli7259
    @patriziopanelli7259 4 роки тому

    Hello, How do you normalized the Chip-seq samples? thanks

  • @ShahzadNSyed
    @ShahzadNSyed 6 років тому +1

    thank you!

  • @jamescameron159
    @jamescameron159 2 роки тому

    Can anyone link me to the fastq files used here?