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spatial

All thing spatial, from MERFISH, to histology

To start discussion on spatial data generation, here are some notes from a recent Lung Seed Network call on designing probesets for targeted spatial methods for merFISH.

Call on 2019.12.02:

Background information:

MerFISH can deal with up to 128 probes

Computational probeset design from scRNA-seq data:

  • can’t be high expression otherwise you get overlaps between pixels due to high-intensity
  • medium to low expression (difficult to map from scRNA-seq)

Current common approach:

  • use cell labels and combinatorially pick out low and medium expressed genes to maximize distances between clusters

Other approach:

  • Jeff Moffit: Bio networks/pathways of interest and grab out all non-high-expression genes, and add some marker genes -> claims this works well

Challenges:

Not clear yet what medium and low expression is yet (esp. when using scRNA-seq as reference)

  • check out what Xiaowei Zhuang’s group used for “highly expressed”
    • Allen Brain group has similar definition

Most of the probe selection has been done on brain:

  • in brain need to separate neuronal subtypes which share a lot of genes, different setup/challenge in lung

Defining markers manually means we face difficulty of cell type vs cell state delineation when we decide what to look for

Ideas:

  • Sasha: probe design to introns so that RNA counts are lower and localized to nucleus
  • include TFs as low expressed genes

Plans for data generation:

Location for spatial data generation:

  • proximal airways or distal alveolar unit:
    • probably use latter, or both

What cell identities do we expect? Distal alveolar unit composition:

  • Type I and Type II cells
  • endothelial cells
  • fibroblasts

Sasha: prefer combination of markers that determine a cell type, not just one

  • BUT: difficulty of cell type vs cell state... what are we looking for?

Doug: could start data generation in Feb

Costs 20-30k for initial probeset, then can use this probeset again after establishing protocols for cheaper

  • need good gene set!

Define scope for computational probeset inference:

  • Fabian: should define a concrete target, i.e. identify cell type with X% accuracy
  • how to valiate? -> first within exp: split data, test on reconstruction performance on rest

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