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powertcr's Introduction

powerTCR: modeling the clone size distribution of the TCR repertoire

This is an R package for fitting the discrete gamma-GPD spliced threshold model to a distribution of clone sizes. The package contains tools needed to perform all of the analyses found in our paper, powerTCR: a model-based approach to comparative analysis of the clone size distribution of the T cell receptor repertoire.

Installation

Install and load this package from BioConductor by typing in R:

if (!requireNamespace("BiocManager", quietly=TRUE))
    install.packages("BiocManager")
BiocManager::install("powerTCR")

or take it directly from from GitHub with:

library(devtools)
install_github("hillarykoch/powerTCR")
library(powerTCR)

Getting going

See the package vignette for a detailed walkthrough of package features.

Citation

You may read our methods paper at PLoS Computational Biology.

If you found the powerTCR package useful, please cite our paper:

Koch H, Starenki D, Cooper SJ, Myers RM, Li Q (2018) powerTCR: A model-based approach to comparative analysis of the clone size distribution of the T cell receptor repertoire. PLOS Computational Biology 14(11): e1006571. https://doi.org/10.1371/journal.pcbi.1006571

Citation for the powerTCR package is:

Koch H (2018). powerTCR: Model-Based Comparative Analysis of the TCR Repertoire. R package version 1.1.4.

powertcr's People

Contributors

hillarykoch avatar link-ny avatar lshep avatar nturaga avatar vobencha avatar

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Forkers

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powertcr's Issues

Are the Shannon Entropy and similar metrics calculated by powerTCR robust against sequencing depth?

Hi @hillarykoch,

I'm trying to compare the TCR repertoires from a bunch of samples, and the number of cells per sample vary from ~350 to ~4000. I tested powerTCR on these samples, and to my understanding this works, I understand that the distances between samples are not biased by the number of cells per sample. So, I can see that samples group the way I expected, but I also want to do a statistical test of a metric that represents something that people know what it is, such as Shannon Entropy. What I don't get is if that is sensitive to sequencing depth, or if that somehow is compensated for in your model? Could you give some advice on a suitable metric?

Reference to the paper

Hi, I have seen you submitted the package to Bioconductor, thanks for doing so.

In the README and in the vignette there are several references to your paper. Could you provide a link or a reference to read more about the models used and the main outcomes of your analysis?

Many thanks

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