BASIC

BASIC assembles full-length antigen receptor gene sequences (BCR and TCR) from single-cell RNA-sequencing (scRNA-seq) data, enabling reconstruction of B-cell receptor (BCR) heavy and light chains at single-cell resolution.


Key Features:

  • Single-Cell Resolution: Assembles BCR sequences from individual B cells using scRNA-seq to recover cell-specific heavy and light chains.
  • Semi-De Novo Assembly Approach: Employs a semi-de novo strategy that combines reference-based and de novo assembly elements tailored for BCR gene reconstruction.
  • Experimental Validation: Validated on nearly 200 single human B cells with single-cell primer-based nested PCR and Sanger sequencing.

Scientific Applications:

  • Profiling BCR Diversity: Enables single-cell–level analysis of BCR sequence diversity and clonality.
  • Antigen Recognition Studies: Facilitates reconstruction of heavy and light chains for studying individual B-cell antigen specificity.
  • Immunology Research: Supports investigation of immune responses, vaccine development, and autoimmune disease by providing full-length receptor sequences.

Methodology:

Integration of scRNA-seq data with a semi-de novo assembly algorithm that combines reference-based and de novo assembly elements to reconstruct full-length heavy and light chain BCR sequences.

Topics

Details

License:
MIT
Maturity:
Emerging
Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Python
Added:
12/1/2018
Last Updated:
12/10/2018

Operations

Publications

Canzar S, Neu KE, Tang Q, Wilson PC, Khan AA. BASIC: BCR assembly from single cells. Bioinformatics. 2016;33(3):425-427. doi:10.1093/bioinformatics/btw631. PMID:28172415. PMCID:PMC5408917.

Funding: - National Institute of Allergy and Infectious Diseases, National Institutes of Health: T32AI007090, U19AI057266, U19AI082724, U19AI109946

Documentation

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