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Related Concept Videos

Genomics02:02

Genomics

41.8K
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...
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Next-generation Sequencing03:00

Next-generation Sequencing

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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....
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RNA-seq03:21

RNA-seq

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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...
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Genome Annotation and Assembly03:36

Genome Annotation and Assembly

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The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
22.0K
Sanger Sequencing01:57

Sanger Sequencing

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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...
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Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes02:16

Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes

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The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
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Related Experiment Video

Updated: Apr 4, 2026

An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing
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An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing

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Heterogeneous Cloud Framework for Big Data Genome Sequencing.

Chao Wang, Xi Li, Peng Chen

    IEEE/ACM Transactions on Computational Biology and Bioinformatics
    |September 11, 2015
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    This study introduces a novel FPGA-based acceleration solution using the MapReduce framework to speed up next-generation genome sequencing. The proposed system offers significant performance improvements for large-scale genomic data analysis with satisfactory accuracy and cost.

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

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    Area of Science:

    • Bioinformatics
    • Computational Biology
    • Big Data Analytics

    Background:

    • Next-generation genome sequencing generates massive datasets, challenging current computational infrastructures.
    • Existing acceleration methods often rely on single approaches, proving insufficient for explosive data scales and complexities.
    • Efficient processing of short and long reads is crucial for advancing genomic research.

    Purpose of the Study:

    • To propose and evaluate a novel FPGA-based acceleration solution integrated with the MapReduce framework for next-generation genome sequencing.
    • To address the limitations of current methodologies in handling large-scale genomic data.
    • To enhance the speed and efficiency of aligning short reads to reference genomes.

    Main Methods:

    • Development of a novel FPGA-based acceleration architecture utilizing the MapReduce framework on multiple hardware accelerators.
    • Theoretical speedup analysis conducted on a MapReduce programming platform.
    • Implementation and evaluation of a hardware prototype on a Xilinx FPGA chip.

    Main Results:

    • Theoretical analysis demonstrated significant potential for speedup in large-scale genome sequencing applications.
    • Experimental evaluation on an FPGA prototype showed efficient acceleration of the next-generation sequencing problem.
    • The proposed platform achieved satisfactory accuracy, mapping quality, and acceptable hardware cost with a low error rate.

    Conclusions:

    • The proposed FPGA-based MapReduce solution effectively accelerates next-generation genome sequencing tasks.
    • This approach offers a viable and efficient method for handling the computational demands of modern genomics.
    • The system provides a balance of performance, accuracy, and cost-effectiveness for genomic data analysis.