AIMC Topic: Sequence Analysis, DNA

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A sequence-based two-layer predictor for identifying enhancers and their strength through enhanced feature extraction.

Journal of bioinformatics and computational biology
Enhancers are short regulatory DNA fragments that are bound with proteins called activators. They are free-bound and distant elements, which play a vital role in controlling gene expression. It is challenging to identify enhancers and their strength ...

DeLUCS: Deep learning for unsupervised clustering of DNA sequences.

PloS one
We present a novel Deep Learning method for the Unsupervised Clustering of DNA Sequences (DeLUCS) that does not require sequence alignment, sequence homology, or (taxonomic) identifiers. DeLUCS uses Frequency Chaos Game Representations (FCGR) of prim...

Table2Vec-automated universal representation learning of enterprise data DNA for benchmarkable and explainable enterprise data science.

Scientific reports
Enterprise data typically involves multiple heterogeneous data sources and external data that respectively record business activities, transactions, customer demographics, status, behaviors, interactions and communications with the enterprise, and th...

GapPredict - A Language Model for Resolving Gaps in Draft Genome Assemblies.

IEEE/ACM transactions on computational biology and bioinformatics
Short-read DNA sequencing instruments can yield over 10 bases per run, typically composed of reads 150 bases long. Despite this high throughput, de novo assembly algorithms have difficulty reconstructing contiguous genome sequences using short reads ...

BreakNet: detecting deletions using long reads and a deep learning approach.

BMC bioinformatics
BACKGROUND: Structural variations (SVs) occupy a prominent position in human genetic diversity, and deletions form an important type of SV that has been suggested to be associated with genetic diseases. Although various deletion calling methods based...

Co-evolution based machine-learning for predicting functional interactions between human genes.

Nature communications
Over the next decade, more than a million eukaryotic species are expected to be fully sequenced. This has the potential to improve our understanding of genotype and phenotype crosstalk, gene function and interactions, and answer evolutionary question...

Deep learning for cancer type classification and driver gene identification.

BMC bioinformatics
BACKGROUND: Genetic information is becoming more readily available and is increasingly being used to predict patient cancer types as well as their subtypes. Most classification methods thus far utilize somatic mutations as independent features for cl...

A Deep Learning-Based Method for Identification of Bacteriophage-Host Interaction.

IEEE/ACM transactions on computational biology and bioinformatics
Multi-drug resistance (MDR) has become one of the greatest threats to human health worldwide, and novel treatment methods of infections caused by MDR bacteria are urgently needed. Phage therapy is a promising alternative to solve this problem, to whi...

T Cell Epitope Prediction and Its Application to Immunotherapy.

Frontiers in immunology
T cells play a crucial role in controlling and driving the immune response with their ability to discriminate peptides derived from healthy as well as pathogenic proteins. In this review, we focus on the currently available computational tools for ep...

iPromoter-ET: Identifying promoters and their strength by extremely randomized trees-based feature selection.

Analytical biochemistry
Promoter is a region of DNA that determines the transcription of a particular gene. There are several σ factors in the RNA polymerase, which has the function of identifying the promoter and facilitating the binding of the RNA polymerase to the promot...