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

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Learn-at-ease

Learn-at-ease

Күн бұрын

Hi,
I am Dr. Dweipayan Goswami,
Welcome to my KZbin channel "Learn at ease"
I will be uploading animated videos related to biochemistry for the Under Graduates and Graduates purely based on the information form the traditional text books
I will also upload videos in the subjects of Microbiology, Biotechnology, Immunology etc.
If you like the concept, please subscribe to my channel 'LEARN AT EASE'

Пікірлер: 20
@user-wv7dn6ux5p
@user-wv7dn6ux5p Жыл бұрын
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.
@pankajbarfal4784
@pankajbarfal4784 Ай бұрын
thank you very much sir, very informative.
@victoriaogor4525
@victoriaogor4525 Ай бұрын
Very useful sir, thanks.
@drmrunalinibr2869
@drmrunalinibr2869 Жыл бұрын
Extremely good explanation
@DweipayanG
@DweipayanG Жыл бұрын
Thank you !!
@bjjjallowjallow7844
@bjjjallowjallow7844 11 ай бұрын
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.
@blessy945
@blessy945 11 ай бұрын
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
@endalineaniefuna9304
@endalineaniefuna9304 4 ай бұрын
Thanks a lot!
@mekpath5818
@mekpath5818 Жыл бұрын
Thank you so much
@anjalighosh13
@anjalighosh13 2 ай бұрын
Sir forward primer always binds with anti sense strand and reverse primer binds with sense strand.
@repallyayyanna7849
@repallyayyanna7849 11 ай бұрын
thanks, its useful video
@kristinacasandrapava9252
@kristinacasandrapava9252 6 ай бұрын
Hi, what do you do when there are gaps between the sequences after aligning them?
@noorlutphyali7495
@noorlutphyali7495 7 ай бұрын
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 ?
@khanhammaadabdulwahab2000
@khanhammaadabdulwahab2000 5 ай бұрын
From where we can download forward and reverse sequences?
@thehippocampus9130
@thehippocampus9130 5 ай бұрын
How about for 4peaks?
@user-wv7dn6ux5p
@user-wv7dn6ux5p Жыл бұрын
please give the website link of bioedit software, bcz there is more than 3-4.
@kajalpanchal8239
@kajalpanchal8239 Жыл бұрын
Hello sir, does forward mean 5 prime to 3 prime?
@DweipayanG
@DweipayanG Жыл бұрын
Forward mean , the amplicon that u get by extension of forward primer
@Zahid.Mumtaz
@Zahid.Mumtaz 4 ай бұрын
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 6 ай бұрын
Sir i have some problems to solving Blast. Can i contact with you through mail or contact number ?
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