Genome Assembly Overview Part 5

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  • เผยแพร่เมื่อ 11 ธ.ค. 2024
  • Overview of genome assembly theory

ความคิดเห็น • 9

  • @samanthabalgobin4115
    @samanthabalgobin4115 3 ปีที่แล้ว +2

    I was very lost in my bioinfomatics comp methods course because I didn't understand what was happening under the hood with the assemblers. Now that I understand the graph theory, everything is starting to flow. Thank you so much for this breakdown. Please continue to post, your videos are saving students who are unfairly paying exorbitant tuition for half assed teaching.

  • @gracesun6971
    @gracesun6971 2 ปีที่แล้ว

    Thank you for sharing the videos. They are not only well explained, but also very interesting.

  • @vishalguptabt
    @vishalguptabt 4 ปีที่แล้ว

    Great job Loren! Thanks for sharing.

  • @joshuathomas8673
    @joshuathomas8673 2 ปีที่แล้ว

    Very clear videos. Thanks a lot!

  • @dundalkholly
    @dundalkholly 4 ปีที่แล้ว

    Great series. Thank you very much

  • @mailaralingams7896
    @mailaralingams7896 5 ปีที่แล้ว

    thank you so muh dear.. it helps lot

  • @Phieliefant
    @Phieliefant 4 ปีที่แล้ว +1

    This might be a stupid question, but I am relatively new to metagenomics and aim to fully understand how genome assemblers work. I am wondering why you would want to break up a contig into its k-mers and then find the eulerian path to just to reconstruct the contig again? I think, I might have missed something. Any answer would be appreciated, thank you.

    • @Phieliefant
      @Phieliefant 4 ปีที่แล้ว

      I mean read, not contig, sorry.

    • @chandankumar-gn5pk
      @chandankumar-gn5pk 3 ปีที่แล้ว +2

      So here comes the indexing part of assembler, many reads might have similar short sequences in between, making k-mers out of reads and than indexing those reads helps in time and memory consumption of an algorithm, coz if we have the information of the index of that k-mer we don't need to reestablish memory for that!