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

Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

6.4K
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...
6.4K

You might also read

Related Articles

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

Sort by
Same author

Mapping the synovial immune ecosystem in rheumatoid arthritis: cellular cartography and pathotype-guided immune restoration.

Current opinion in immunology·2026
Same author

Double vs. single autologous stem cell transplantation in patients with multiple myeloma and high-risk factors: A systematic review and meta-analysis.

Oncology letters·2026
Same author

LUMINEX technology detects plasma inflammatory factor expression levels in children with severe and non-severe community acquired pneumonia.

BMC pediatrics·2026
Same author

Diffusion-enhanced Fine-grained Cross Semantic Fusion for Drug-disease Association Prediction.

IEEE journal of biomedical and health informatics·2026
Same author

Diagnostic value of unilateral adrenal vein sampling with simple and biochemical/imaging correction: a study on early screening and typing for primary aldosteronism.

BMC endocrine disorders·2026
Same author

Bisphenols, nonylphenols, and nonylphenol metabolites in paired dust and urine across China: insights into systemic oxidative stress.

Environment international·2026

Related Experiment Video

Updated: Oct 8, 2025

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

12.2K

AMC: accurate mutation clustering from single-cell DNA sequencing data.

Zhenhua Yu1,2, Fang Du1,2

  • 1School of Information Engineering, Ningxia University, Yinchuan 750021, China.

Bioinformatics (Oxford, England)
|December 24, 2021
PubMed
Summary

Accurate Mutation Clustering (AMC) software improves phylogenetic inference from large single-cell DNA sequencing datasets by efficiently clustering mutations. This enhances computational efficiency and accuracy for analyzing intra-tumor heterogeneity.

More Related Videos

Characterizing Mutational Load and Clonal Composition of Human Blood
07:58

Characterizing Mutational Load and Clonal Composition of Human Blood

Published on: July 11, 2019

7.5K
Detection of Copy Number Alterations Using Single Cell Sequencing
09:45

Detection of Copy Number Alterations Using Single Cell Sequencing

Published on: February 17, 2017

11.8K

Related Experiment Videos

Last Updated: Oct 8, 2025

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

12.2K
Characterizing Mutational Load and Clonal Composition of Human Blood
07:58

Characterizing Mutational Load and Clonal Composition of Human Blood

Published on: July 11, 2019

7.5K
Detection of Copy Number Alterations Using Single Cell Sequencing
09:45

Detection of Copy Number Alterations Using Single Cell Sequencing

Published on: February 17, 2017

11.8K

Area of Science:

  • Genomics
  • Computational Biology
  • Cancer Research

Background:

  • Single-cell DNA sequencing (scDNA-seq) provides high-resolution intra-tumor heterogeneity profiles.
  • Current phylogenetic inference methods struggle with computational efficiency and accuracy on large scDNA-seq datasets.

Purpose of the Study:

  • To introduce Accurate Mutation Clustering (AMC), a novel software for efficient phylogenetic inference from scDNA-seq data.
  • To improve the accuracy and computational efficiency of analyzing large-scale single-cell genomic data.

Main Methods:

  • AMC utilizes Principal Component Analysis (PCA) and K-means clustering to group mutations.
  • It infers maximum likelihood estimates for genotypes within mutation clusters.
  • Phylogenetic trees are reconstructed using these inferred genotypes.

Main Results:

  • AMC demonstrates high computational efficiency in clustering mutations on large scDNA-seq datasets.
  • The method improves the accuracy of phylogenetic inference compared to existing approaches.
  • Evaluations on simulated datasets confirm AMC's utility for large-scale analyses.

Conclusions:

  • AMC offers a significant advancement in analyzing intra-tumor heterogeneity using scDNA-seq data.
  • The software enhances the efficiency and accuracy of phylogenetic tree reconstruction.
  • AMC is a valuable tool for researchers working with large single-cell genomic datasets.