Alevin efficiently estimates accurate gene abundances from dscRNA-seq data
We introduce alevin, a fast end-to-end pipeline to process droplet-based single-cell RNA sequencing data, performing cell barcode detection, read mapping, unique molecular identifier (UMI) deduplication, gene count estimation, and cell barcode whitelisting. Alevin’s approach to UMI deduplication con...
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| Veröffentlicht in: | Genome Biology Jg. 20; H. 1; S. 65 |
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| Sprache: | Englisch |
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London
BioMed Central
27.03.2019
Springer Nature B.V BMC |
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| ISSN: | 1474-760X, 1474-7596, 1474-760X |
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| Abstract | We introduce alevin, a fast end-to-end pipeline to process droplet-based single-cell RNA sequencing data, performing cell barcode detection, read mapping, unique molecular identifier (UMI) deduplication, gene count estimation, and cell barcode whitelisting. Alevin’s approach to UMI deduplication considers transcript-level constraints on the molecules from which UMIs may have arisen and accounts for both gene-unique reads and reads that multimap between genes. This addresses the inherent bias in existing tools which discard gene-ambiguous reads and improves the accuracy of gene abundance estimates. Alevin is considerably faster, typically eight times, than existing gene quantification approaches, while also using less memory. |
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| AbstractList | We introduce alevin, a fast end-to-end pipeline to process droplet-based single-cell RNA sequencing data, performing cell barcode detection, read mapping, unique molecular identifier (UMI) deduplication, gene count estimation, and cell barcode whitelisting. Alevin's approach to UMI deduplication considers transcript-level constraints on the molecules from which UMIs may have arisen and accounts for both gene-unique reads and reads that multimap between genes. This addresses the inherent bias in existing tools which discard gene-ambiguous reads and improves the accuracy of gene abundance estimates. Alevin is considerably faster, typically eight times, than existing gene quantification approaches, while also using less memory.We introduce alevin, a fast end-to-end pipeline to process droplet-based single-cell RNA sequencing data, performing cell barcode detection, read mapping, unique molecular identifier (UMI) deduplication, gene count estimation, and cell barcode whitelisting. Alevin's approach to UMI deduplication considers transcript-level constraints on the molecules from which UMIs may have arisen and accounts for both gene-unique reads and reads that multimap between genes. This addresses the inherent bias in existing tools which discard gene-ambiguous reads and improves the accuracy of gene abundance estimates. Alevin is considerably faster, typically eight times, than existing gene quantification approaches, while also using less memory. We introduce alevin, a fast end-to-end pipeline to process droplet-based single-cell RNA sequencing data, performing cell barcode detection, read mapping, unique molecular identifier (UMI) deduplication, gene count estimation, and cell barcode whitelisting. Alevin’s approach to UMI deduplication considers transcript-level constraints on the molecules from which UMIs may have arisen and accounts for both gene-unique reads and reads that multimap between genes. This addresses the inherent bias in existing tools which discard gene-ambiguous reads and improves the accuracy of gene abundance estimates. Alevin is considerably faster, typically eight times, than existing gene quantification approaches, while also using less memory. Abstract We introduce alevin, a fast end-to-end pipeline to process droplet-based single-cell RNA sequencing data, performing cell barcode detection, read mapping, unique molecular identifier (UMI) deduplication, gene count estimation, and cell barcode whitelisting. Alevin’s approach to UMI deduplication considers transcript-level constraints on the molecules from which UMIs may have arisen and accounts for both gene-unique reads and reads that multimap between genes. This addresses the inherent bias in existing tools which discard gene-ambiguous reads and improves the accuracy of gene abundance estimates. Alevin is considerably faster, typically eight times, than existing gene quantification approaches, while also using less memory. |
| ArticleNumber | 65 |
| Author | Sudbery, Ian Srivastava, Avi Patro, Rob Malik, Laraib Smith, Tom |
| Author_xml | – sequence: 1 givenname: Avi surname: Srivastava fullname: Srivastava, Avi organization: Department of Computer Science, Stony Brook University – sequence: 2 givenname: Laraib surname: Malik fullname: Malik, Laraib organization: Department of Computer Science, Stony Brook University – sequence: 3 givenname: Tom surname: Smith fullname: Smith, Tom organization: Cambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge – sequence: 4 givenname: Ian surname: Sudbery fullname: Sudbery, Ian organization: Sheffield Institute for Nucleic Acids, Department of Molecular Biology and Biotechnology, The University of Sheffield – sequence: 5 givenname: Rob orcidid: 0000-0001-8463-1675 surname: Patro fullname: Patro, Rob email: rob.patro@cs.stonybrook.edu organization: Department of Computer Science, Stony Brook University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30917859$$D View this record in MEDLINE/PubMed |
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| Keywords | Cellular barcode UMI deduplication Quantification Single-cell RNA-seq |
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| Title | Alevin efficiently estimates accurate gene abundances from dscRNA-seq data |
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