<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zath GK</submitter><funding>Defense Advanced Research Projects Agency</funding><funding>Montana State University</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>Materials Research Science and Engineering Center, Harvard University</funding><funding>National Science Foundation</funding><pagination>4735-4745</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10016142</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(23)</volume><pubmed_abstract>In drop-based microfluidics, an aqueous sample is partitioned into drops using individual pump sources that drive water and oil into a drop-making device. Parallelization of drop-making devices is necessary to achieve high-throughput screening of multiple experimental conditions, especially in time-sensitive studies. Here, we present the plate-interfacing parallel encapsulation (PIPE) chip, a microfluidic chip designed to generate 50 to 90 μm diameter drops of up to 96 different conditions in parallel by interfacing individual drop makers with a standard 384-well microtiter plate. The PIPE chip is used to generate two types of optically barcoded drop libraries consisting of two-color fluorescent particle combinations: a library of 24 microbead barcodes and a library of 192 quantum dot barc</pubmed_abstract><journal>Lab on a chip</journal><pubmed_title>Rapid parallel generation of a fluorescently barcoded drop library from a microtiter plate using the plate-interfacing parallel encapsulation (PIPE) chip.</pubmed_title><pmcid>PMC10016142</pmcid><funding_grant_id>CAREER DMR-1753352</funding_grant_id><funding_grant_id>DMR-2011754</funding_grant_id><funding_grant_id>R21 AI151923</funding_grant_id><funding_grant_id>1R21Al151923</funding_grant_id><funding_grant_id>SP 1282/1-1</funding_grant_id><funding_grant_id>W911NF-17-2-0034</funding_grant_id><pubmed_authors>Zath GK</pubmed_authors><pubmed_authors>Hoffman CW</pubmed_authors><pubmed_authors>Chang CB</pubmed_authors><pubmed_authors>Bikos DA</pubmed_authors><pubmed_authors>Abate AR</pubmed_authors><pubmed_authors>Sperling RA</pubmed_authors><pubmed_authors>Abbasi R</pubmed_authors><pubmed_authors>Weitz DA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid parallel generation of a fluorescently barcoded drop library from a microtiter plate using the plate-interfacing parallel encapsulation (PIPE) chip.</name><description>In drop-based microfluidics, an aqueous sample is partitioned into drops using individual pump sources that drive water and oil into a drop-making device. Parallelization of drop-making devices is necessary to achieve high-throughput screening of multiple experimental conditions, especially in time-sensitive studies. Here, we present the plate-interfacing parallel encapsulation (PIPE) chip, a microfluidic chip designed to generate 50 to 90 μm diameter drops of up to 96 different conditions in parallel by interfacing individual drop makers with a standard 384-well microtiter plate. The PIPE chip is used to generate two types of optically barcoded drop libraries consisting of two-color fluorescent particle combinations: a library of 24 microbead barcodes and a library of 192 quantum dot barc</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-21T16:13:43.141Z</modification><creation>2025-04-21T16:13:43.141Z</creation></dates><accession>S-EPMC10016142</accession><cross_references><pubmed>36367139</pubmed><doi>10.1039/d2lc00909a</doi></cross_references></HashMap>