4.4. Next Generation Sequencing - Practice Session : Variant Calling

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  • Опубликовано: 16 сен 2024

Комментарии • 8

  • @JenniFadoni
    @JenniFadoni 3 года назад +1

    Very clear explanation. Thank you very much

  • @camilocarias5501
    @camilocarias5501 3 года назад +1

    Hello, how do I determine the correct filtering threshold in VCFfilter? There is a minimum threshold value? Should I use 200 as a correct filtering threshold or can I use a 220 based on my first result?

  • @dylandog2841
    @dylandog2841 3 года назад +1

    From a multisample vcf file
    how can get only a subset heterozygous (1/2) using VCFfilter?

  • @elenips7231
    @elenips7231 2 года назад

    Very helpful video , thank you!! I am not really familiar with bioinformatics and in this part of my project, I am trying two compare two VCF files corresponding to the results of healthy tissue and tumor tissue. I want to compare these VCF files and remove their similarities. More specific I want to remove the information of the healthy tissue from the tumor one. Have you any suggestions on which tool I should use or any way that I can do my analysis? thank you in advance!

  • @niusha3323
    @niusha3323 3 года назад +1

    Anyone else here hopeless after the coursera project? Lol

  • @AyrodsGamgam
    @AyrodsGamgam Год назад

    bioinfo is overrated, lots of tools become obsolete,.