8.2. Human Genomic Variations - Practice Session : Types of Human Genomic Variations

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  • Опубликовано: 7 ноя 2024

Комментарии • 10

  • @ifyifemanima3972
    @ifyifemanima3972 2 года назад

    Hello, do you know the best tool for generating VCF files from multiple sequences at once?

  • @harshitpardhi4541
    @harshitpardhi4541 Год назад

    can you explain how to use snpEff to annotate vcf file of e.coli k12

  • @genomicsandbioinformatics9628
    @genomicsandbioinformatics9628 4 года назад +3

    Very informative session. Great work. Please make a tutorial on snpeff. How to customize snpeff according to our needs. I mean how can we do variant annotation on snpeff for a list of snps that we mostly get after genome wide association. Thanks

    • @kusumy2620
      @kusumy2620 3 года назад

      hey i also want to enquire the same. please help!!

  • @danhatechav
    @danhatechav 11 месяцев назад

    Thanks!

  • @felipebatalini
    @felipebatalini 2 года назад

    Exceptional! Very focused and practical!

  • @madhavanjn
    @madhavanjn 2 года назад

    Very nice bro, thank you so much.

  • @ashamerin
    @ashamerin 3 года назад

    Concise! Brilliant

  • @BrandonNewell222
    @BrandonNewell222 2 года назад

    So well done, thank you

  • @serychristianrenaud
    @serychristianrenaud 2 года назад

    Thank