Course: Analyzing amplicon sequencing data with Qiime 2 - Pt. 1

  Рет қаралды 18,173

Institute for Systems Biology

Institute for Systems Biology

Күн бұрын

Пікірлер: 8
@szymonjakubowski3574
@szymonjakubowski3574 Жыл бұрын
5:11 Introduction to QUIIME 2 notebook, setting up enviorment 10:45 Introduction to QUIIME alghorytm 17:07 16SrRNA amplicon sequencing vs shotgun metagenomics 21:40 Metagenomics use in diagnosing recurrent C.differens infection 27:49 General workflow in QUIIME 16SrRNA analysis 28:44 Illumina FastQ file structure 36:03 Running first QUIMME command- importing fastq data as artifacts 41:57 Demultiplexing, creating quality visualisations of demultiplexed data 49:51 Denoising amplicon sequence variants in QUIIME 52:10 DADA2- plugin functions 54:10 DADA2- ASV Identification 57:19 DADA2- PCR Chimeras problem 1:01:42 DADA2- Merging 1:04:34 DADA2- visualisations 1:07:29 Diversity metrics- alpha and beta diversity 1:19:24 Principal Coordinate Analysis (PCoA) in phylogenetic tree construction 1:22:50 Beta diversity: 3D Emperor visualisation of PCoA 1:23:40 Statistical tests for beta diversity with PERMANOVA 1:27:57 Creating taxonomy based on sequences with Multinomial Naive Bayes 1:35:12 Final barplot visualisations 1:38:40 Creating heatmap of microbiota for samples
@quangvinhnguyen114
@quangvinhnguyen114 Ай бұрын
Thank you so much
@Caroline-vy1co
@Caroline-vy1co Жыл бұрын
Thanks for sharing this! it was very helpful.
@ikraminf
@ikraminf Жыл бұрын
Thanks for sharing such an informative video. I wanted to know what things metadata.tsv file contains i.e., the column names?
@soulbrother12
@soulbrother12 4 жыл бұрын
Question: At 49:05 you mention that cutting off the first nt´s would be conservative...what exactly do you mean by that ( gerne auch auf deutsch :-) ) And thanks so much for the upload!!!
@AqleemAbbas
@AqleemAbbas 3 жыл бұрын
It means the first nts have normally high quality do just remove barcode & adaper
@adeelabbasi7375
@adeelabbasi7375 Жыл бұрын
important question. can we perform QIIME2 analysis in a 24 hour time for 16 samples of roughly 100K reads each.????
@asadhaq7819
@asadhaq7819 4 жыл бұрын
Dear Christian Diener, Thanks a lot for such an informative video presentation. It is a problem solver for me. However, I lost the track before Excercise 2. What is the code just before the Excercise 2> Secondly, can we use this program to analyze our own data?
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