Related Experiment Video
Updated: Dec 10, 2025

09:40
Novel Sequence Discovery by Subtractive Genomics
Published on: January 25, 2019
9.0K
Decombinator V4: an improved AIRR compliant-software package for T-cell receptor sequence annotation?
Thomas Peacock1,2, James M Heather3, Tahel Ronel1,4
1Division of Infection and Immunity, UCL, WC1E 6BT, London, UK.
Bioinformatics (Oxford, England)
|August 28, 2020
Summary
Researchers can now accurately annotate T-cell receptor (TCR) sequences using Decombinator V4. This updated Python tool enhances analysis of cellular immunity data with improved error correction and standard-compliant output.
Area of Science:
- Immunology
- Bioinformatics
- Computational Biology
Background:
- T-cell receptor (TCR) repertoire analysis is crucial for understanding cellular immunity.
- Annotating TCR sequences from raw data presents challenges due to non-germline encoding and stochastic generation.
- Existing tools require updates to handle increasing sequence data volumes and complexity.
Purpose of the Study:
- To release Decombinator V4, an improved software tool for TCR sequence annotation.
- To provide researchers with an accurate and fast method for analyzing large TCR repertoire datasets.
- To ensure compatibility with international standards for adaptive immune receptor repertoire research.
Main Methods:
- Development of Decombinator V4 as a Python software package.
- Implementation of improved algorithms for sequencing error and PCR bias correction.
- Ensuring output compatibility with Adaptive Immune Receptor Repertoire Community standards.
Main Results:
- Decombinator V4 offers accurate and fast annotation of large TCR sequence sets.
- The updated package provides Python 3 compatibility.
- New algorithms enhance data quality by correcting sequencing errors and PCR bias.
Conclusions:
- Decombinator V4 is a valuable, freely available tool for TCR repertoire analysis.
- The software facilitates standardized and high-quality analysis of cellular immunity data.
- This advancement supports researchers in the rapidly growing field of immune repertoire sequencing.
More Related Videos
Related Concept Videos
RNA-seq
11.4K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
11.4K
Genome Annotation and Assembly
20.2K
The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
20.2K
Cis-regulatory Sequences
3.8K
3.8K
Cis-regulatory Sequences
11.3K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
11.3K
RACE - Rapid Amplification of cDNA Ends
6.9K
Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
6.9K
Complementary DNA
30.9K
Overview
30.9K

