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BASIC: BCR assembly from single cells
Author(s) -
Stefan Canzar,
Karlynn E. Neu,
Qingming Tang,
Patrick C. Wilson,
Aly A. Khan
Publication year - 2016
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btw631
Subject(s) - computational biology , single cell analysis , rna , sanger sequencing , biology , dna sequencing , single cell sequencing , rna seq , primer (cosmetics) , software , cell , computer science , dna , genetics , gene expression , gene , chemistry , transcriptome , organic chemistry , programming language , exome sequencing , mutation
The B-cell receptor enables individual B cells to identify diverse antigens, including bacterial and viral proteins. While advances in RNA-sequencing (RNA-seq) have enabled high throughput profiling of transcript expression in single cells, the unique task of assembling the full-length heavy and light chain sequences from single cell RNA-seq (scRNA-seq) in B cells has been largely unstudied.

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