Identify split reads in given chromosomal regions
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Updated
Oct 29, 2017 - C++
Identify split reads in given chromosomal regions
(Under development) Computational framework for probabilistic models of immune receptor assembling.
TCR Enrichment Analysis (TEA) Webtool
Suit of statistical procedures for robust quantification of various BCR and TCR repertoire properties
Statistical classifier for diagnosing ovarian cancer from immune repertoires
MSc Bioinformatics with Systems Biology Dissertation
Adversarial autoencoders for MHCI epitope and immunogenicity prediction
Limitations of machine learning models for specificity prediction of T-cell receptor sequences
T-cell receptor specificity prediction using Deep Learning
Prediction and characterization of T cell response by improved T cell receptors to antigen specificity with interpretable deep learning
Prediction and characterization of T cell response by improved T cell receptors to antigen specificity with interpretable deep learning
The Read Origin Protocol (ROP) is a computational protocol that aims to discover the source of all reads, including those originating from repeat sequences, recombinant B and T cell receptors, and microbial communities.
Benchmarking modern neural networks for scRNA sequencing analysis
[Deprecated, see https://github.com/antigenomics/mirpy and other tools @antigenomics] Post-analysis of immune repertoire sequencing data
HTS-compatible wrapper for IgBlast V-(D)-J mapping tool
TCR embedding expressivity evaluation framework.
A nextflow pipeline for TCR repertoire building with MiXCR
TCR Epitope Generation Model with Top-K Prediction
Standardise TR/MH/IG data
Clustering of immune receptor repertoires
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