Benchmarking computational methods for B-cell receptor reconstruction from single-cell RNA-seq data. Issue 3 (13th July 2022)
- Record Type:
- Journal Article
- Title:
- Benchmarking computational methods for B-cell receptor reconstruction from single-cell RNA-seq data. Issue 3 (13th July 2022)
- Main Title:
- Benchmarking computational methods for B-cell receptor reconstruction from single-cell RNA-seq data
- Authors:
- Andreani, Tommaso
Slot, Linda M
Gabillard, Samuel
Strübing, Carsten
Reimertz, Claus
Yaligara, Veeranagouda
Bakker, Aleida M
Olfati-Saber, Reza
Toes, René E M
Scherer, Hans U
Augé, Franck
Šimaitė, Deimantė - Abstract:
- Abstract: Multiple methods have recently been developed to reconstruct full-length B-cell receptors (BCRs) from single-cell RNA sequencing (scRNA-seq) data. This need emerged from the expansion of scRNA-seq techniques, the increasing interest in antibody-based drug development and the importance of BCR repertoire changes in cancer and autoimmune disease progression. However, a comprehensive assessment of performance-influencing factors such as the sequencing depth, read length or number of somatic hypermutations (SHMs) as well as guidance regarding the choice of methodology is still lacking. In this work, we evaluated the ability of six available methods to reconstruct full-length BCRs using one simulated and three experimental SMART-seq datasets. In addition, we validated that the BCRs assembled in silico recognize their intended targets when expressed as monoclonal antibodies. We observed that methods such as BALDR, BASIC and BRACER showed the best overall performance across the tested datasets and conditions, whereas only BASIC demonstrated acceptable results on very short read libraries. Furthermore, the de novo assembly-based methods BRACER and BALDR were the most accurate in reconstructing BCRs harboring different degrees of SHMs in the variable domain, while TRUST4, MiXCR and BASIC were the fastest. Finally, we propose guidelines to select the best method based on the given data characteristics.
- Is Part Of:
- NAR genomics and bioinformatics. Volume 4:Issue 3(2022)
- Journal:
- NAR genomics and bioinformatics
- Issue:
- Volume 4:Issue 3(2022)
- Issue Display:
- Volume 4, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 4
- Issue:
- 3
- Issue Sort Value:
- 2022-0004-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-07-13
- Subjects:
- Genomics -- Periodicals
Bioinformatics -- Periodicals
572.8 - Journal URLs:
- http://www.oxfordjournals.org/ ↗
https://academic.oup.com/nargab ↗ - DOI:
- 10.1093/nargab/lqac049 ↗
- Languages:
- English
- ISSNs:
- 2631-9268
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22547.xml