<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Choi J</submitter><funding>National Research Foundation of Korea</funding><pagination>157</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9063264</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Although single-cell RNA sequencing of xenograft samples has been widely used, no comprehensive bioinformatics pipeline is available for human and mouse mixed single-cell analyses. Considering the numerous homologous genes across the human and mouse genomes, misalignment errors should be evaluated, and a new algorithm is required. We assessed the extents and effects of misalignment errors and exonic multi-mapping events when using human and mouse combined reference data and developed a new bioinformatics pipeline with expression-based species deconvolution to minimize errors. We also evaluated false-positive signals presumed to originate from ambient RNA of the other species and address the importance to computationally remove them.&lt;h4>Result&lt;/h4>Error when using combined reference account for an average of 0.78% of total reads, but such reads were concentrated to few genes that were greatly affected. Human and mouse mixed single-cell data, analyzed using our pipeline, clustered well with unmixed data and showed higher k-nearest-neighbor batch effect test and Local Inverse Simpson's Index scores than those derived from Cell Ranger (10 × Genomics). We also applied our pipeline to multispecies multisample single-cell library containing breast cancer xenograft tissue and successfully identified all samples using genomic array and expression. Moreover, diverse cell types in the tumor microenvironment were well captured.&lt;h4>Conclusion&lt;/h4>We present our bioinformatics pipeline for mixed human and mouse single-cell data, which can also be applied to pooled libraries to obtain cost-effective single-cell data. We also address misalignment, multi-mapping error, and ambient RNA as a major consideration points when analyzing multispecies single-cell data.</pubmed_abstract><journal>BMC bioinformatics</journal><pubmed_title>Expression-based species deconvolution and realignment removes misalignment error in multispecies single-cell data.</pubmed_title><pmcid>PMC9063264</pmcid><funding_grant_id>2020R1A2C3012524</funding_grant_id><pubmed_authors>Lee CH</pubmed_authors><pubmed_authors>Kim JI</pubmed_authors><pubmed_authors>Moon HG</pubmed_authors><pubmed_authors>Choi J</pubmed_authors><pubmed_authors>Cho S</pubmed_authors><pubmed_authors>Yang HK</pubmed_authors><pubmed_authors>Lee W</pubmed_authors><pubmed_authors>Choi SM</pubmed_authors><pubmed_authors>Chung JH</pubmed_authors><pubmed_authors>Yoon JK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Expression-based species deconvolution and realignment removes misalignment error in multispecies single-cell data.</name><description>&lt;h4>Background&lt;/h4>Although single-cell RNA sequencing of xenograft samples has been widely used, no comprehensive bioinformatics pipeline is available for human and mouse mixed single-cell analyses. Considering the numerous homologous genes across the human and mouse genomes, misalignment errors should be evaluated, and a new algorithm is required. We assessed the extents and effects of misalignment errors and exonic multi-mapping events when using human and mouse combined reference data and developed a new bioinformatics pipeline with expression-based species deconvolution to minimize errors. We also evaluated false-positive signals presumed to originate from ambient RNA of the other species and address the importance to computationally remove them.&lt;h4>Result&lt;/h4>Error when using combined reference account for an average of 0.78% of total reads, but such reads were concentrated to few genes that were greatly affected. Human and mouse mixed single-cell data, analyzed using our pipeline, clustered well with unmixed data and showed higher k-nearest-neighbor batch effect test and Local Inverse Simpson's Index scores than those derived from Cell Ranger (10 × Genomics). We also applied our pipeline to multispecies multisample single-cell library containing breast cancer xenograft tissue and successfully identified all samples using genomic array and expression. Moreover, diverse cell types in the tumor microenvironment were well captured.&lt;h4>Conclusion&lt;/h4>We present our bioinformatics pipeline for mixed human and mouse single-cell data, which can also be applied to pooled libraries to obtain cost-effective single-cell data. We also address misalignment, multi-mapping error, and ambient RNA as a major consideration points when analyzing multispecies single-cell data.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-05-18T12:44:10.539Z</modification><creation>2025-05-18T12:44:10.539Z</creation></dates><accession>S-EPMC9063264</accession><cross_references><pubmed>35501695</pubmed><doi>10.1186/s12859-022-04676-0</doi></cross_references></HashMap>