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2023_cytominer_sphering_benchmark's Introduction

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Goal

We aim to answer the question: Does sphering the morphological profiles improve retrievability?

Steps

We integrate different modules of pycytominer with Shantanu’s sphering.

Download data

Fetch specific scripts to preprocess data

Resources and notes

Method discussion

The method is

  1. estimate sphering transform across all negcon wells from all batches, then apply this transform to all wells (including negcon)
  2. estimate a sphering transform per batch (across all negcon wells from the batch), then apply the transform to each corresponding batch

Currently, we do only 1. We discussed: why do 1 at all if we are doing 2? The way to think about is to consider the corresponding data generation model:

Consider the data frame comprising all N batches X = {X_i} i=1…N X_i is a n_i x d dimensional matrix (n_i wells x d features)

This X is the true data that we are trying to estimate, but we can observe only Z = {Z_i} i=1…N Z_i is a n_i x p dimensional matrix (n_i wells x p features) To keep this simpler, we assume p = d

Z_i = global_variation(local_variation_i(X_i))

location_variation_i = batch-specific scaling, rotation, and translation of X_i global_variation = batch-agnostic scaling, rotation, and translation of local_variation_i(X_i)

#1 removes global variation, #2 removes location variation

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