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Longitudinal high-throughput TCR repertoire profiling reveals the dynamics of T cell memory formation after mild COVID-19 infection

<p>Processed TCRbeta and TCRalpha repertoires after mild COVID-19 (Version 2.0: day 85 timepoints added) infection,&nbsp;see&nbsp;preprint:&nbsp;<a href="https://www.biorxiv.org/content/10.1101/2020.05.18.100545v3">https://www.biorxiv.org/content/10.1101/2020.05.18.100545v3</a></p> <p>and GitHub repository:&nbsp;<a href="https://github.com/pogorely/Minervina_COVID">https://github.com/pogorely/Minervina_COVID</a></p> <p>Two donors (M and W), two biological replicates of PBMC&nbsp;(F1 and F2), CD4+, CD8+, and Memory subpopulations&nbsp;for each post-infection time points (day 15, 30, 37, 45, 85 post-infection), and pre-infection PBMC repertoires sampled in 2019 and 2018.&nbsp;</p>

ShareScore

44/100

Overall dataset sharing score

Score breakdown

These five areas show where the dataset supports — or may limit — practical reuse.

Stewardship
8
Harmonization
4
Access
16
Reuse readiness
8
Engagement
8

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