MIT CompBio Lecture 21 - Single-Cell Genomics

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  • เผยแพร่เมื่อ 31 พ.ค. 2024
  • MIT Computational Biology: Genomes, Networks, Evolution, Health
    Prof. Manolis Kellis
    compbio.mit.edu/6.047/
    Fall 2018
    Lecture 21 - Single-cell Genomics
    1. Single-cell profiling technologies
    - Traditional single-cell analyses
    - Single-cell RNA-seq
    - Dealing with noise in scRNA-seq data
    - Single-cell epigenomics (scATAC-Seq)
    2. Extracting biological insights from single-cell data
    - Clustering similar cells
    - Clustering similar genes
    - Dimensionality reduction
    - Distinguishing different cell types
    - Trajectories through cell space
    - Dataset completion and missing data imputation
    3. Single-cell RNA-seq in disease: Focus on Brain Disorders
    - Why Brain: Cell type and function diversity
    - Initial maps of brain diversity across regions, development, organoids
    - Brain variation at the single-cell level in Alzheimer’s disease
    - Somatic mosaicism and clonality from scDNA-seq and scRNA-seq
    - Deconvolution of bulk data into single-cell profiles vs. phenotype vs. genotype
    - Deconvolution of eQTL effects at single-cell level and mediation analysis
    Slides for Lecture 21:
    stellar.mit.edu/S/course/6/fa...

ความคิดเห็น • 18

  •  ปีที่แล้ว +1

    Thank you so much Dr. Manolis Kellis. Greetings from Bimac Research Group at Universidad del Cauca, Colombia.

  • @qsc9546
    @qsc9546 3 ปีที่แล้ว +1

    PCA to construct network, with network molecularity reduction usually has up to 0.8 clustering accuracy with low noise field dataset.

  • @laylachae
    @laylachae 5 ปีที่แล้ว

    Thank you very much. It helped me a lot.

  • @timazebardast1096
    @timazebardast1096 4 ปีที่แล้ว +4

    Thank you, I really enjoyed this lecture, comprehensive, nice speech, good voice and video quality. 💜

  • @lhsilhs1512
    @lhsilhs1512 4 ปีที่แล้ว

    Dr. Kellis, Thank you. Is this the entire lecture that you offered for scRNA-seq methods or are there more lectures that we can learn.

  • @lvest79
    @lvest79 4 ปีที่แล้ว +1

    Great lecture!

  • @chaks94
    @chaks94 3 ปีที่แล้ว

    Very clearly explained! Thank you so much.

  • @qsc9546
    @qsc9546 3 ปีที่แล้ว +1

    What's the overall performance of Seurat, Scanpy, SingleR, and ScPred ? Really depends on data sets.

  • @educationk
    @educationk 3 ปีที่แล้ว +1

    Awesome lecture...is there way to find codes for all the plots generated here?

  • @anjalimaru823
    @anjalimaru823 3 ปีที่แล้ว

    Is it also applicable for mitochondrial and chloroplast genomics ????

  • @OmegaPsiPhi0
    @OmegaPsiPhi0 5 ปีที่แล้ว +2

    Human Cell Atlas 📚

  • @helenaklarajambor2914
    @helenaklarajambor2914 4 ปีที่แล้ว

    Super great for preparing my own lectures, thank you very much Manolis! Did anyone catch the Barcoding: I think he said with 10 nucleotides there are 2^10 possibilities, does that mean for barcodes only 2 nucleotides are used? Else i'd be 4^10 possibilities?

  • @olgaantonova5939
    @olgaantonova5939 4 ปีที่แล้ว

    nice intro, but every 10 seconds, he says "you know".

    • @ManolisKellis1
      @ManolisKellis1  4 ปีที่แล้ว +2

      Thanks for your feedback Olga, i'll be more careful in the future

    • @Singularitarian
      @Singularitarian 4 ปีที่แล้ว +5

      @@ManolisKellis1 Saying "you know" is fine, I didn't even notice. Not a bad thing.