Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

RNA-seq03:21

RNA-seq

11.5K
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...
11.5K
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

18.4K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
18.4K
Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

4.5K
Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scale  studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved...
4.5K
Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

6.7K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
6.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A spatially resolved human glioblastoma atlas reveals distinct cellular and molecular patterns of anatomical niches.

Nature communications·2026
Same author

Colorectal microenvironment determines the prognosis of colorectal cancer.

Experimental & molecular medicine·2026
Same author

Pan-Cancer Single-Cell RNA Sequencing Analysis Refines Multi-Origin Monocyte and Macrophage Lineages.

Cancer immunology research·2025
Same author

Towards fair decentralized benchmarking of healthcare AI algorithms with the Federated Tumor Segmentation (FeTS) challenge.

Nature communications·2025
Same author

Pan-Cancer Analysis of Oncogenic MET Fusions Reveals Distinct Pathogenomic Subsets with Differential Sensitivity to MET-Targeted Therapy.

Cancer discovery·2025
Same author

Multi-Omics Analysis of Glioblastoma and Glioblastoma Cell Line: Molecular Insights Into the Functional Role of GPR56 and TG2 in Mesenchymal Transition.

Frontiers in oncology·2022
Same journal

Application of ephrin-B2 loaded glycol chitosan-silk fibroin hydrogel in the treatment of diabetic refractory wounds.

Scientific reports·2026
Same journal

International expert Delphi consensus on thromboprophylaxis in metabolic and bariatric surgery.

Scientific reports·2026
Same journal

Assessing the cross-region knowledge transfer capability of selected deep learning building vectorization methods in the context of available training datasets.

Scientific reports·2026
Same journal

Feasibility and preliminary effects of outdoor versus indoor cognitive-motor therapy in women with Alzheimer's disease: A randomized single-blind pilot study.

Scientific reports·2026
Same journal

Hallmarks of social action in the vocal turn-taking of wild common marmosets (Callithrix jacchus).

Scientific reports·2026
Same journal

Role and mechanism of AOPPs-induced NOX4-mediated ferroptosis in intervertebral disc degeneration.

Scientific reports·2026
See all related articles

Related Experiment Video

Updated: Dec 16, 2025

Novel Sequence Discovery by Subtractive Genomics
09:40

Novel Sequence Discovery by Subtractive Genomics

Published on: January 25, 2019

9.0K

Recursive Consensus Clustering for novel subtype discovery from transcriptome data.

Pranali Sonpatki1, Nameeta Shah2

  • 1Mazumdar Shaw Center for Translational Research, Mazumdar Shaw Medical Foundation, Narayana Hrudayalaya Health City, Bangalore, India.

Scientific Reports
|July 5, 2020
PubMed
Summary
This summary is machine-generated.

Recursive Consensus Clustering (RCC) aids biologists in discovering novel cell subtypes from large transcriptomic datasets. This unsupervised algorithm simplifies identifying optimal clusters and generating biological insights.

More Related Videos

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

12.4K
Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms
10:41

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms

Published on: May 9, 2017

9.5K

Related Experiment Videos

Last Updated: Dec 16, 2025

Novel Sequence Discovery by Subtractive Genomics
09:40

Novel Sequence Discovery by Subtractive Genomics

Published on: January 25, 2019

9.0K
Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

12.4K
Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms
10:41

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms

Published on: May 9, 2017

9.5K

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Large-scale transcriptomic data analysis is crucial for identifying molecular patterns and cell subpopulations.
  • Clustering is a widely used technique for dimensionality reduction and analyzing large biological datasets.
  • A key challenge in clustering is determining the optimal number of clusters (k) to reveal meaningful biological insights.

Purpose of the Study:

  • To develop an unsupervised clustering algorithm for novel subtype discovery from transcriptomic data.
  • To address the challenge of selecting the optimal number of clusters in biological datasets.
  • To provide a tool for both bulk and single-cell transcriptomic data analysis.

Main Methods:

  • Development of Recursive Consensus Clustering (RCC), an unsupervised algorithm.
  • Application of RCC to large-scale transcriptomic datasets (bulk and single-cell).
  • Implementation of RCC as an R package for user accessibility.

Main Results:

  • Successful identification of novel molecular patterns and cell subpopulations.
  • Demonstration of RCC's capability in determining optimal clustering parameters.
  • Facilitation of new biological insights through intuitive visualization of results.

Conclusions:

  • Recursive Consensus Clustering (RCC) is an effective unsupervised algorithm for novel subtype discovery in transcriptomic data.
  • RCC provides a robust solution for determining the optimal number of clusters, enhancing biological data analysis.
  • The R package facilitates the generation of biological insights from both bulk and single-cell datasets.