How to correctly analyze raw sequence files of bacterial 16s rRNA partial gene sequence

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  • Опубликовано: 7 окт 2022
  • Hi,
    I am Dr. Dweipayan Goswami,
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Комментарии • 20

  • @victoriaogor4525
    @victoriaogor4525 14 дней назад

    Very useful sir, thanks.

  • @user-wv7dn6ux5p
    @user-wv7dn6ux5p 10 месяцев назад +1

    Thank you so much for making this fantastic video. I have watched 10 videos by after this video all doubts become clear. if it is possible, please make some video on shotgun whole genome sequencing of bacteria.

  • @dr.mdashrafulislam2864
    @dr.mdashrafulislam2864 Год назад

    need more video about analysis. thank you very much

  • @repallyayyanna7849
    @repallyayyanna7849 10 месяцев назад

    thanks, its useful video

  • @endalineaniefuna9304
    @endalineaniefuna9304 2 месяца назад +1

    Thanks a lot!

  • @anjalighosh13
    @anjalighosh13 21 день назад

    Sir forward primer always binds with anti sense strand and reverse primer binds with sense strand.

  • @mekpath5818
    @mekpath5818 Год назад +1

    Thank you so much

  • @bjjjallowjallow7844
    @bjjjallowjallow7844 9 месяцев назад +2

    how did you get the chromatogram in bioedit. i am only getting the sequence in bioedit and did not know how you opened both the bioedit and chromatogram to delete uncorrect nucleotides.

  • @drmrunalinibr2869
    @drmrunalinibr2869 Год назад +1

    Extremely good explanation

  • @kristinacasandrapava9252
    @kristinacasandrapava9252 4 месяца назад

    Hi, what do you do when there are gaps between the sequences after aligning them?

  • @blessy945
    @blessy945 9 месяцев назад

    sir the lesson is useful. can u also make a video on "how to align our trimmed consensus 16s rRNA sequence with BLAST hit sequences, including some whole genome sequences hits in MEGA software". Thank you

  • @khanhammaadabdulwahab2000
    @khanhammaadabdulwahab2000 3 месяца назад

    From where we can download forward and reverse sequences?

  • @user-wv7dn6ux5p
    @user-wv7dn6ux5p 10 месяцев назад

    please give the website link of bioedit software, bcz there is more than 3-4.

  • @noorlutphyali7495
    @noorlutphyali7495 6 месяцев назад

    The quary length in this example is 403 , i used the same step and i get 665, please i want to ask is this query length acceptable to be be submitted to NCBI to register the bacteria ?

  • @kajalpanchal8239
    @kajalpanchal8239 Год назад +1

    Hello sir, does forward mean 5 prime to 3 prime?

    • @DweipayanG
      @DweipayanG  Год назад

      Forward mean , the amplicon that u get by extension of forward primer

  • @thehippocampus9130
    @thehippocampus9130 3 месяца назад

    How about for 4peaks?

  • @Zahid.Mumtaz
    @Zahid.Mumtaz 2 месяца назад

    Please guide me, I am stuck as my consensus sequence is coming in this form. what to do? Example
    >Consensus -------------------------------------------CTGCCAGTAAGACAGGGATAACGCCCGGAAAC-GAAGCAAATAACGCATA--AACCACTCCGCCAGGGGAG-ACGATCGAAAGACGGAAACGCAAAGCAATT---GACGGGCCCCCGCA-CAAGAGCTAGAGCATGAGGTA-AAGGCGAACCAACGCAAAGAACCATACCAGACCTG-GACA-TCATCGGACA-ACT----CT-AGACCAAAAAACAAGGCTCAACCC-GGAGGGTAAGCGGAAACTCGCCAGCCCGAAA-CACCCAGATAATCC-------------------

  • @rupahalder6723
    @rupahalder6723 5 месяцев назад

    Sir i have some problems to solving Blast. Can i contact with you through mail or contact number ?