<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li M</submitter><funding>NCI NIH HHS</funding><funding>The Hope Foundation</funding><pagination>btae431</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11246167</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>40(7)</volume><pubmed_abstract>&lt;h4>Motivation&lt;/h4>T cell receptors (TCRs) constitute a major component of our adaptive immune system, governing the recognition and response to internal and external antigens. Studying the TCR diversity via sequencing technology is critical for a deeper understanding of immune dynamics. However, library sizes differ substantially across samples, hindering the accurate estimation/comparisons of alpha diversities. To address this, researchers frequently use an overall rarefying approach in which all samples are sub-sampled to an even depth. Despite its pervasive application, its efficacy has never been rigorously assessed.&lt;h4>Results&lt;/h4>In this paper, we develop an innovative "multi-bin" rarefying approach that partitions samples into multiple bins according to their library sizes, conduct</pubmed_abstract><journal>Bioinformatics (Oxford, England)</journal><pubmed_title>A multi-bin rarefying method for evaluating alpha diversities in TCR sequencing data.</pubmed_title><pmcid>PMC11246167</pmcid><funding_grant_id>U10 CA180819</funding_grant_id><funding_grant_id>U10CA180819</funding_grant_id><pubmed_authors>Hua X</pubmed_authors><pubmed_authors>Zhao N</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Wu MC</pubmed_authors><pubmed_authors>Li M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A multi-bin rarefying method for evaluating alpha diversities in TCR sequencing data.</name><description>&lt;h4>Motivation&lt;/h4>T cell receptors (TCRs) constitute a major component of our adaptive immune system, governing the recognition and response to internal and external antigens. Studying the TCR diversity via sequencing technology is critical for a deeper understanding of immune dynamics. However, library sizes differ substantially across samples, hindering the accurate estimation/comparisons of alpha diversities. To address this, researchers frequently use an overall rarefying approach in which all samples are sub-sampled to an even depth. Despite its pervasive application, its efficacy has never been rigorously assessed.&lt;h4>Results&lt;/h4>In this paper, we develop an innovative "multi-bin" rarefying approach that partitions samples into multiple bins according to their library sizes, conduct</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-03T05:34:01.65Z</modification><creation>2026-04-24T03:14:33.72Z</creation></dates><accession>S-EPMC11246167</accession><cross_references><pubmed>38950175</pubmed><doi>10.1093/bioinformatics/btae431</doi></cross_references></HashMap>