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A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples
RNA-Sequencing (RNA-Seq) of peripheral blood can be a valuable source of information for investigating the status and mechanism of diseases. However, blood contains 50–80% unwanted hemoglobin (Hb) transcripts. Lexogen’s QuantSeq mRNA-Seq-Kit for Illumina RNA-Seq features a ‘Globin Block’ (GB) module...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101437/ https://www.ncbi.nlm.nih.gov/pubmed/32221409 http://dx.doi.org/10.1038/s41598-020-62637-0 |
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author | Uellendahl-Werth, Florian Wolfien, Markus Franke, Andre Wolkenhauer, Olaf Ellinghaus, David |
author_facet | Uellendahl-Werth, Florian Wolfien, Markus Franke, Andre Wolkenhauer, Olaf Ellinghaus, David |
author_sort | Uellendahl-Werth, Florian |
collection | PubMed |
description | RNA-Sequencing (RNA-Seq) of peripheral blood can be a valuable source of information for investigating the status and mechanism of diseases. However, blood contains 50–80% unwanted hemoglobin (Hb) transcripts. Lexogen’s QuantSeq mRNA-Seq-Kit for Illumina RNA-Seq features a ‘Globin Block’ (GB) module that depletes Hb cDNAs during library preparation. Here, we aimed to assess GB’s effectiveness and checked for technical biases attributable to GB. Using whole blood total RNA samples of 91 healthy individuals, we sequenced 91 pairs of GB and non-blocked samples (noGB) on Illumina HiSeq2500 and 8 pairs of GB/noGB technical replicates on HiSeq4000. GB reduced the fraction of Hb transcripts from 43% (s.d. 14%) to 8.0% (s.d. 4.3%). From GB samples we detected 1,397 more expressed genes at approximately 11 million reads per RNA-isolate. Enrichment and differential expression analyses did not reveal significant differences for GB and noGB samples with respect to molecular function. In contrast to results from studies that have examined the performance of GB during RNA isolation, we were able to assign GB to corresponding noGB samples (from multiple sequencing runs on HiSeq2500) with at least 89.8% accuracy from the complete correlation matrix of all GB/GB, noGB/noGB and GB/noGB pairs. However, the use of different sequencers (HiSeq2500 vs HiSeq4000) impaired assignment of technical replicates, whereas assignment of GB to corresponding noGB samples worked perfectly when sequencing on one lane on HiSeq4000. Lexogen’s GB RNA-Seq module is a valuable addition during mRNA-Seq library preparation which works even with low amounts of input total RNA (50 ng per sample). GB facilitated the detection of low abundant transcripts and yielded more non-hemoglobin reads, while preserving biological information. We observed that differences in sequencing run and platform have a far greater effect on technical variation than the use of GB. |
format | Online Article Text |
id | pubmed-7101437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71014372020-03-31 A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples Uellendahl-Werth, Florian Wolfien, Markus Franke, Andre Wolkenhauer, Olaf Ellinghaus, David Sci Rep Article RNA-Sequencing (RNA-Seq) of peripheral blood can be a valuable source of information for investigating the status and mechanism of diseases. However, blood contains 50–80% unwanted hemoglobin (Hb) transcripts. Lexogen’s QuantSeq mRNA-Seq-Kit for Illumina RNA-Seq features a ‘Globin Block’ (GB) module that depletes Hb cDNAs during library preparation. Here, we aimed to assess GB’s effectiveness and checked for technical biases attributable to GB. Using whole blood total RNA samples of 91 healthy individuals, we sequenced 91 pairs of GB and non-blocked samples (noGB) on Illumina HiSeq2500 and 8 pairs of GB/noGB technical replicates on HiSeq4000. GB reduced the fraction of Hb transcripts from 43% (s.d. 14%) to 8.0% (s.d. 4.3%). From GB samples we detected 1,397 more expressed genes at approximately 11 million reads per RNA-isolate. Enrichment and differential expression analyses did not reveal significant differences for GB and noGB samples with respect to molecular function. In contrast to results from studies that have examined the performance of GB during RNA isolation, we were able to assign GB to corresponding noGB samples (from multiple sequencing runs on HiSeq2500) with at least 89.8% accuracy from the complete correlation matrix of all GB/GB, noGB/noGB and GB/noGB pairs. However, the use of different sequencers (HiSeq2500 vs HiSeq4000) impaired assignment of technical replicates, whereas assignment of GB to corresponding noGB samples worked perfectly when sequencing on one lane on HiSeq4000. Lexogen’s GB RNA-Seq module is a valuable addition during mRNA-Seq library preparation which works even with low amounts of input total RNA (50 ng per sample). GB facilitated the detection of low abundant transcripts and yielded more non-hemoglobin reads, while preserving biological information. We observed that differences in sequencing run and platform have a far greater effect on technical variation than the use of GB. Nature Publishing Group UK 2020-03-27 /pmc/articles/PMC7101437/ /pubmed/32221409 http://dx.doi.org/10.1038/s41598-020-62637-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Uellendahl-Werth, Florian Wolfien, Markus Franke, Andre Wolkenhauer, Olaf Ellinghaus, David A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples |
title | A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples |
title_full | A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples |
title_fullStr | A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples |
title_full_unstemmed | A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples |
title_short | A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples |
title_sort | benchmark of hemoglobin blocking during library preparation for mrna-sequencing of human blood samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101437/ https://www.ncbi.nlm.nih.gov/pubmed/32221409 http://dx.doi.org/10.1038/s41598-020-62637-0 |
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