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

11.4K
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...
11.4K
Sanger Sequencing01:57

Sanger Sequencing

770.6K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
770.6K
Next-generation Sequencing03:00

Next-generation Sequencing

97.0K
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.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
97.0K

You might also read

Related Articles

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

Sort by
Same author

QutRNA2: robust tRNA modification discovery from Nanopore direct tRNA sequencing.

NAR genomics and bioinformatics·2026
Same author

Accelign: a GPU-based library for accelerating pairwise sequence alignment.

BMC bioinformatics·2026
Same author

gpuPairHMM: High-Speed Pair-HMM Forward Algorithm for DNA Variant Calling on GPUs.

IEEE transactions on computational biology and bioinformatics·2026
Same author

RMapAlign3N: fast mapping of 3N-Reads.

Bioinformatics advances·2025
Same author

GPU-accelerated homology search with MMseqs2.

Nature methods·2025
Same author

Corrigendum to Studying Privacy Aspects of Learned Knowledge Bases in the Context of Synthetic and Medical Data.

Studies in health technology and informatics·2025

Related Experiment Video

Updated: Dec 12, 2025

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
14:06

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

Published on: June 23, 2012

15.6K

RabbitQC: high-speed scalable quality control for sequencing data.

Zekun Yin1,2, Hao Zhang1, Meiyang Liu1

  • 1School of Software, Shandong University, Jinan, China.

Bioinformatics (Oxford, England)
|August 14, 2020
PubMed
Summary
This summary is machine-generated.

RabbitQC is a new, fast quality control tool for FASTQ files generated by modern sequencing technologies. It significantly speeds up pre-processing, making genomic data analysis more efficient.

More Related Videos

Optimization for Sequencing and Analysis of Degraded FFPE-RNA Samples
07:30

Optimization for Sequencing and Analysis of Degraded FFPE-RNA Samples

Published on: June 8, 2020

12.5K
High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq
09:06

High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq

Published on: October 5, 2018

10.6K

Related Experiment Videos

Last Updated: Dec 12, 2025

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
14:06

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

Published on: June 23, 2012

15.6K
Optimization for Sequencing and Analysis of Degraded FFPE-RNA Samples
07:30

Optimization for Sequencing and Analysis of Degraded FFPE-RNA Samples

Published on: June 8, 2020

12.5K
High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq
09:06

High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq

Published on: October 5, 2018

10.6K

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Next-generation sequencing technologies generate large, error-prone datasets.
  • Quality control of FASTQ files is crucial for downstream genomic applications.
  • Existing tools often fail to leverage modern hardware, resulting in slow processing times.

Purpose of the Study:

  • To develop an efficient and integrated quality control tool for FASTQ files.
  • To accelerate the pre-processing of sequencing data by utilizing modern computing capabilities.

Main Methods:

  • Development of RabbitQC, a quality control tool implemented in C++.
  • Optimization for parallel processing and full utilization of hardware capabilities.
  • Integration of various quality control operations for different sequencing platforms.

Main Results:

  • RabbitQC offers significant speedups, achieving one to two orders-of-magnitude faster runtimes compared to existing tools.
  • The tool supports multiple sequencing technologies including Illumina, Oxford Nanopore, and PacBio.
  • Provides integrated quality control operations for enhanced FASTQ file pre-processing.

Conclusions:

  • RabbitQC provides a highly efficient solution for FASTQ file quality control.
  • The tool's speed and versatility make it valuable for modern genomics and medicine.
  • Accelerated data pre-processing facilitates faster and more effective biological data analysis.