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bcr-repertoire-papers's Introduction

Awesome BCR repertoire papers ๐Ÿ“

B cell receptor (BCR) repertoire analysis has grown tremendously in the last 10 years, transforming our understanding disease and enabling the discovery of novel therapeutics. We at Alchemab love the huge growth in this space and have curated a list of papers across several areas. This is not an exhaustive list, so please let us know if we've missed your favourite paper.

We intend this to be a growing list, so if you'd like to contribute, or suggest any new categories, feel free to submit a pull request.

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Table of contents

Reviews

BCR repertoire datasets

Notes

We refer readers to the Observed Antibody Space (OAS) database and the Paired OAS database as the most straight-forward resources for obtaining amino acid sequence datasets for e.g. machine learning applications.

For simplicity, we're mentioning articles that are not already covered by OAS. We focus on papers where authors have uploaded datasets as part of the publication (with no login/registration required) or via public repositories such as the NIH SRA, requiring minimal admin overhead. Publications that only provide V gene + J gene + CDR3 are not mentioned here.

Machine learning

Notes

The remit of this section is to cover how machine learning (ML) methods have been trained using BCR repertoire data, or applying existing ML tools for enhancing repertoire analyses. Due to the nature of the way things are moving in this space, quite a few publications are just pre-prints!

Clonotyping Methods

Notes

The remit of this section is to cover "methods papers" that focus on how to identify clonotypes from immune BCR repertoire datasets.

Structural annotations

Notes

The remit of this section is to cover how structure prediction methods (such as ABodyBuilder) can be used to interrogate and understand "structural convergence" of the BCR repertoire. We'd like to point readers to the latest structure prediction tools in this space, including ABLooper, DeepAb, and of course AlphaFold2.

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