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Related Concept Videos

RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

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 primer.
Since the...
Gene Duplication and Divergence02:37

Gene Duplication and Divergence

The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
Improving Translational Accuracy02:07

Improving Translational Accuracy

Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
Improving Translational Accuracy02:07

Improving Translational Accuracy

Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
RNA-seq03:21

RNA-seq

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. 
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Next-generation Sequencing

The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
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Although all next-generation methods use different technologies, they all share a set of standard features.

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Related Experiment Video

Updated: Jun 17, 2026

Comprehensive Spatial Profiling of Species-agnostic Transcriptomes via Stereo-seq
10:22

Comprehensive Spatial Profiling of Species-agnostic Transcriptomes via Stereo-seq

Published on: October 31, 2025

RSTG: Robust Generation of High Quality Spatial Transcriptomics Data using Beta Divergence Based AutoEncoder.

Agrya Halder, Abhik Ghosh, Sanghamitra Bandyopadhyay

    IEEE Journal of Biomedical and Health Informatics
    |June 15, 2026
    PubMed
    Summary
    This summary is machine-generated.

    Robust Spatial Transcriptomic Generator (RSTG) creates realistic synthetic spatial transcriptomics data. This generative model effectively handles noisy data, improving analysis accuracy and stability.

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    Mining Spatial Transcriptomics Datasets using DeepSpaceDB
    10:16

    Mining Spatial Transcriptomics Datasets using DeepSpaceDB

    Published on: September 5, 2025

    Related Experiment Videos

    Last Updated: Jun 17, 2026

    Comprehensive Spatial Profiling of Species-agnostic Transcriptomes via Stereo-seq
    10:22

    Comprehensive Spatial Profiling of Species-agnostic Transcriptomes via Stereo-seq

    Published on: October 31, 2025

    Mining Spatial Transcriptomics Datasets using DeepSpaceDB
    10:16

    Mining Spatial Transcriptomics Datasets using DeepSpaceDB

    Published on: September 5, 2025

    Area of Science:

    • Computational Biology
    • Genomics
    • Bioinformatics

    Background:

    • Spatial transcriptomics analysis faces challenges due to limited training data.
    • Existing generative models struggle with noisy data, including outliers.
    • Developing robust methods for synthetic data generation is crucial for advancing spatial transcriptomics.

    Purpose of the Study:

    • To propose RSTG (Robust Spatial Transcriptomic Generator), a novel autoencoder model.
    • To enhance the generation of realistic and high-quality spatial transcriptomic sequences.
    • To improve the robustness of generative models against data noise and outliers.

    Main Methods:

    • Developed RSTG, an autoencoder incorporating the beta-ELBO loss.
    • Utilized variational inference to approximate data distribution and density estimation.
    • Validated the model on diverse spatial transcriptomics datasets (MERFISH, MERSCOPE, Visium).

    Main Results:

    • RSTG demonstrated improved performance in generating high-quality spatial transcriptomic data.
    • The model effectively recovered cellular positions in 2D spatial and location domains.
    • RSTG maintained data quality and stability even with contaminated training data (outliers, batch effects, dropouts).

    Conclusions:

    • RSTG offers a robust solution for generating synthetic spatial transcriptomics data.
    • The model's ability to handle noise enhances its applicability in real-world scenarios.
    • RSTG advances spatial transcriptomics analysis by providing reliable synthetic data for model training.