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Related Concept Videos

Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
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. 
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lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA (lncRNA)...
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...
DNA Microarrays02:34

DNA Microarrays

Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
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Protein Networks

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Related Experiment Video

Updated: May 26, 2026

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved (Non-model) Organisms
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CrossQuery: a web tool for easy associative querying of transcriptome data.

Toni U Wagner1, Andreas Fischer, Eva C Thoma

  • 1Physiological Chemistry I, Biocenter, University of Würzburg, Würzburg, Germany. toni.wagner@biozentrum.uni-wuerzburg.de

Plos One
|December 17, 2011
PubMed
Summary

CrossQuery is a web tool simplifying transcriptome sequencing and microarray data analysis for researchers. It allows easy filtering, sorting, and correlation of complex biological datasets with minimal computational expertise.

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Area of Science:

  • Bioinformatics
  • Genomics
  • Computational Biology

Background:

  • Modern sequencing technologies generate vast biological datasets.
  • Complex primary analyses require specialist expertise.
  • Biomedical researchers need accessible tools for secondary data analysis.

Purpose of the Study:

  • To introduce CrossQuery, a web tool for non-specialists.
  • To enable straightforward querying of transcriptome sequencing and microarray data.
  • To facilitate data filtering, sorting, and cross-association.

Main Methods:

  • Development of a web-based tool, CrossQuery.
  • Utilized deep-sequencing data from Medaka fish stem cells.
  • Employed microarray data from human endothelial cells.
  • Implemented simple syntax for data queries.

Main Results:

  • CrossQuery allows correlation, filtering, and sorting of mRNA expression, gene/transcript IDs, GO-terms, and gene descriptions.
  • Queries can be saved and results exported to standard formats compatible with tools like Microsoft Excel.
  • The tool supports the association of multiple datasets sharing common identifiers (e.g., transcript IDs, GO-terms).

Conclusions:

  • CrossQuery empowers researchers to work with complex omics data efficiently.
  • Minimal computer skills are required for effective data exploration.
  • The tool's design supports extensibility for advanced users and new data types.