<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Yu P</submitter><funding>NCATS NIH HHS</funding><pubmed_abstract>Inference from immunological data on cells in the adaptive immune system may benefit from modeling specifications that describe variation in the sizes of various clonal sub-populations. We develop one such specification in order to quantify the effects of surrogate selection assays, which we confirm may lead to an enrichment for amplified, potentially disease-relevant T cell clones. Our specification couples within-clonotype birth-death processes with an exchangeable model across clonotypes. Beyond enrichment questions about the surrogate selection design, our framework enables a study of sampling properties of elementary sample diversity statistics; it also points to new statistics that may usefully measure the burden of somatic genomic alterations associated with clonal expansion. We exa</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2023.07.13.548950</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10369934</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>SURROGATE SELECTION OVERSAMPLES EXPANDED T CELL CLONOTYPES.</pubmed_title><pmcid>PMC10369934</pmcid><funding_grant_id>UL1 TR002373</funding_grant_id><pubmed_authors>Albertini RJ</pubmed_authors><pubmed_authors>Yu P</pubmed_authors><pubmed_authors>Lian Y</pubmed_authors><pubmed_authors>Albertini MR</pubmed_authors><pubmed_authors>Newton MA</pubmed_authors><pubmed_authors>Zuleger CL</pubmed_authors></additional><is_claimable>false</is_claimable><name>SURROGATE SELECTION OVERSAMPLES EXPANDED T CELL CLONOTYPES.</name><description>Inference from immunological data on cells in the adaptive immune system may benefit from modeling specifications that describe variation in the sizes of various clonal sub-populations. We develop one such specification in order to quantify the effects of surrogate selection assays, which we confirm may lead to an enrichment for amplified, potentially disease-relevant T cell clones. Our specification couples within-clonotype birth-death processes with an exchangeable model across clonotypes. Beyond enrichment questions about the surrogate selection design, our framework enables a study of sampling properties of elementary sample diversity statistics; it also points to new statistics that may usefully measure the burden of somatic genomic alterations associated with clonal expansion. We exa</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jul</publication><modification>2025-08-23T03:09:10.393Z</modification><creation>2025-08-23T03:09:10.393Z</creation></dates><accession>S-EPMC10369934</accession><cross_references><pubmed>37503118</pubmed><doi>10.1101/2023.07.13.548950</doi></cross_references></HashMap>