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SCSit: A high-efficiency preprocessing tool for single-cell sequencing data from SPLiT-seq.
Luan, Mei-Wei; Lin, Jia-Lun; Wang, Ye-Fan; Liu, Yu-Xiao; Xiao, Chuan-Le; Wu, Rongling; Xie, Shang-Qian.
Afiliación
  • Luan MW; Key Laboratory of Genetics and Germplasm Innovation of Tropical Special Forest Trees and Ornamental Plants (Ministry of Education), School of Life Science, Hainan University, Haikou 570228, China.
  • Lin JL; College of Biomedical Information and Engineering, Hainan Medical University, Haikou 571199, China.
  • Wang YF; Key Laboratory of Genetics and Germplasm Innovation of Tropical Special Forest Trees and Ornamental Plants (Ministry of Education), School of Life Science, Hainan University, Haikou 570228, China.
  • Liu YX; College of Biomedical Information and Engineering, Hainan Medical University, Haikou 571199, China.
  • Xiao CL; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China.
  • Wu R; Public Health Sciences and Statistics and Center for Statistical Genetics, Pennsylvania State University, Hershey, PA, USA.
  • Xie SQ; Key Laboratory of Genetics and Germplasm Innovation of Tropical Special Forest Trees and Ornamental Plants (Ministry of Education), School of Life Science, Hainan University, Haikou 570228, China.
Comput Struct Biotechnol J ; 19: 4574-4580, 2021.
Article en En | MEDLINE | ID: mdl-34471500
SPLiT-seq provides a low-cost platform to generate single-cell data by labeling the cellular origin of RNA through four rounds of combinatorial barcoding. However, an automatic and rapid method for preprocessing and classifying single-cell sequencing (SCS) data from SPLiT-seq, which directly identified and labeled combinatorial barcoding reads and distinguished special cell sequencing data, is currently lacking. Here, we develop a high-efficiency preprocessing tool for single-cell sequencing data from SPLiT-seq (SCSit), which can directly identify combinatorial barcodes and UMI of cell types and obtain more labeled reads, and remarkably enhance the retained data from SCS due to the exact alignment of insertion and deletion. Compared with the original method used in SPLiT-seq, the consistency of identified reads from SCSit increases to 97%, and mapped reads are twice than the original. Furthermore, the runtime of SCSit is less than 10% of the original. It can accurately and rapidly analyze SPLiT-seq raw data and obtain labeled reads, as well as effectively improve the single-cell data from SPLiT-seq platform. The data and source of SCSit are available on the GitHub website https://github.com/shang-qian/SCSit.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Comput Struct Biotechnol J Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Comput Struct Biotechnol J Año: 2021 Tipo del documento: Article País de afiliación: China
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