Related Experiment Video

Updated: Apr 17, 2026

Identifying Transcription Factor Olig2 Genomic Binding Sites in Acutely Purified PDGFRα+ Cells by Low-cell Chromatin Immunoprecipitation Sequencing Analysis
12:29

Identifying Transcription Factor Olig2 Genomic Binding Sites in Acutely Purified PDGFRα+ Cells by Low-cell Chromatin Immunoprecipitation Sequencing Analysis

Published on: April 16, 2018

9.8K

Detecting differential peaks in ChIP-seq signals with ODIN

Manuel Allhoff, Kristin Seré, Heike Chauvistré

    Bioinformatics (Oxford, England)
    |February 13, 2015
    PubMed
    Summary

    No abstract available in PubMed .

    More Related Videos

    Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance
    04:58

    Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance

    Published on: December 13, 2024

    4.9K
    Sampling and Analysis of Animal Scent Signals
    14:59

    Sampling and Analysis of Animal Scent Signals

    Published on: February 13, 2021

    5.3K

    Related Experiment Videos

    Last Updated: Apr 17, 2026

    Identifying Transcription Factor Olig2 Genomic Binding Sites in Acutely Purified PDGFRα+ Cells by Low-cell Chromatin Immunoprecipitation Sequencing Analysis
    12:29

    Identifying Transcription Factor Olig2 Genomic Binding Sites in Acutely Purified PDGFRα+ Cells by Low-cell Chromatin Immunoprecipitation Sequencing Analysis

    Published on: April 16, 2018

    9.8K
    Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance
    04:58

    Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance

    Published on: December 13, 2024

    4.9K
    Sampling and Analysis of Animal Scent Signals
    14:59

    Sampling and Analysis of Animal Scent Signals

    Published on: February 13, 2021

    5.3K

    Related Concept Videos

    Comparing Copy Number Variations and SNPs02:26

    Comparing Copy Number Variations and SNPs

    19.4K
    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%...
    19.4K
    ¹³C NMR: ¹H–¹³C Decoupling01:04

    ¹³C NMR: ¹H–¹³C Decoupling

    2.2K
    The probability of having two carbon-13 atoms next to each other is negligible because of the low natural abundance of carbon-13. Consequently, peak splitting due to carbon-carbon spin-spin coupling is not observed in spectra. However, protons up to three sigma bonds away split the carbon signal according to the n+1 rule, resulting in complicated spectra.
    A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
    2.2K

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

    Developmental factors drive the compartmentalized and discontinuous maturation of the small intestinal epithelium during the early postnatal period.

    PLoS biology·2026

    CAR T-cells targeting CD117 effectively eliminate mast cells in preclinical models of advanced systemic mastocytosis.

    Leukemia·2026

    Protocol for generating megakaryocytes from patient induced pluripotent stem cells for disease modeling and compound screening.

    STAR protocols·2026

    Wnt-dependent spatiotemporal reprogramming of bone marrow niches drives fibrosis.

    HemaSphere·2026

    PHLOWER leverages single-cell multimodal data to infer complex, multi-branching cell differentiation trajectories.

    Nature methods·2025

    PILOT-GM-VAE: patient-level analysis of single-cell disease atlas with optimal transport of Gaussian mixture variational autoencoders.

    Briefings in bioinformatics·2025

    Drug target prediction from perturbation transcriptomics via a biological function-guided hypergraph siamese network.

    Bioinformatics (Oxford, England)·2026

    When Multimodal Fusion Fails: Contrastive Alignment as a Necessary Stabilizer for TCR-Peptide Binding Prediction.

    Bioinformatics (Oxford, England)·2026

    ConfRetro: A 3D-aware Template-free Method for Enhancing Retrosynthesis via Molecular Conformer Information.

    Bioinformatics (Oxford, England)·2026

    Assessing the influence of different alignment tools on the accuracy of a forensic epigenetic clock.

    Bioinformatics (Oxford, England)·2026

    Trans-dimensional Bayesian model averaging for 13C-metabolic flux analysis: Evidence-based flux inference under structural model uncertainty.

    Bioinformatics (Oxford, England)·2026

    DeepGeSeq: Deep learning library for Genomic Sequence modeling and analysis.

    Bioinformatics (Oxford, England)·2026

    Reduced glymphatic function in autism revealed by the diffusion tensor analysis along the perivascular space index.

    Journal of neural transmission (Vienna, Austria : 1996)·2026

    [Ethical and clinical aspects of genetic analysis in neurodegenerative diseases].

    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova·2026

    Interpreting molecular evidence for biosecurity decision-making: Lessons from coconut rhinoceros beetle incursions in the Pacific.

    Current research in insect science·2026

    Post-transcriptional regulation via alternative polyadenylation and piRNA shapes macrophage responses in psoriasis.

    Frontiers in immunology·2026

    DNA Replication Stress-Induced Transcriptome of Human Burkitt's Lymphoma Identifies Reciprocal Regulation Between MBD1 and BCL6 During Germinal Center-Derived B-Lymphomagenesis.

    Hematological oncology·2026

    From linear models to deep learning: statistical advances in genomic selection for animal breeding.

    Journal of animal science and biotechnology·2026
    See all related articles
    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
    Jove
    Visualize
    Contact Us