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Related Concept Videos

Genomics02:02

Genomics

Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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...
Next-generation Sequencing03:00

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.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
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. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...

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Related Experiment Video

Updated: May 15, 2026

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms
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Paean: A Unified and Efficient Transcriptome Quantification System Using Heterogeneous Computing.

Jiefu Li1, Jiawen Guan2, Jiaqiang Qian3

  • 1Guangzhou National Laboratory, Guangzhou 510005, China.

Journal of Molecular Biology
|March 26, 2026
PubMed
Summary
This summary is machine-generated.

Paean, a new GPU-CPU parallel computing system, significantly accelerates RNA sequencing data analysis for gene expression and alternative splicing. This tool offers over 100-fold speed improvement with comparable accuracy, enabling large-scale genomic studies and cancer immunotherapy applications.

Keywords:
GPURNA splicinggene expressionheterogeneous computationtranscriptome quantification

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • RNA sequencing (RNA-seq) data analysis demands high computational performance.
  • Existing CPU-based pipelines are resource-intensive and slow for large datasets, limiting gene expression and alternative splicing analysis.
  • There is a need for efficient computational methods to handle the growing volume of RNA-seq data.

Purpose of the Study:

  • To develop a high-performance parallel computing system for rapid RNA-seq data analysis.
  • To integrate efficient algorithms for calculating gene expression levels and alternative splicing ratios.
  • To validate the accuracy, reliability, and applicability of the developed system on massive datasets.

Main Methods:

  • Developed Paean, a parallel computing system utilizing GPU-CPU platforms.
  • Integrated two efficient, highly parallel algorithms into a unified pipeline.
  • Tested Paean on various computational platforms and large-scale datasets, including the TCGA dataset.

Main Results:

  • Paean achieves comparable quantification precision to existing methods.
  • Paean is over 100-fold faster than existing methods, requiring significantly less computation resource.
  • Successful analysis of the complete TCGA dataset (10,866 samples) in 3,400 minutes demonstrates excellent performance on massive datasets.

Conclusions:

  • Paean provides a rapid and efficient solution for analyzing large RNA-seq datasets.
  • The system facilitates the identification of tumor neoantigen candidates from RNA splicing events, with applications in cancer immunotherapy and precision medicine.
  • Paean is open-source, promoting accessibility and further development in the field.