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accession-icon ERP005567
Generation of a de novo trascriptome assembly from equine lamellar tissue
  • organism-icon Equus caballus
  • sample-icon 3 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

The equine hoof is a specialized structure in which the distal skeleton is suspended within the capsule by interdigitated structures known as laminae. Inflammation of this tissue, known as laminitis, is a devastating disease that is the second leading cause of both lameness and euthanasia in the horse. Current research on the laminitic transcriptome focuses on the expression of known genes. However, as this tissue is quite unique and equine annotation is largely derived from computational predictions and gene models from other species, there are likely yet uncharacterized transcripts expressed in the laminae that may be involved in the etiology of laminitis. In order to create a novel annotation resource, we performed whole transcriptome sequencing of sagittal lamellar sections from one control and two laminitis affected horses. Assembly of 113 million 100bp reads resulted in around 75,000 transcripts. Of these, 36,000 corresponded to known annotation in NCBI's non-redundant protein database. RT-PCR of 12 selected annotations confirmed structure and expression in lamellar tissue. Transcriptome sequencing represents a powerful tool to expand on equine annotation and identify novel targets for further laminitis research.

Publication Title

No associated publication

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP149598
Cardiac gene expression in two broiler lines at two different time points
  • organism-icon Gallus gallus
  • sample-icon 20 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Male broilers from two lines (n=10 per line) with different growth rate were raised at the same condition with free access to feed and drink. At day 6 and day 21, half samples of each broiler line were euthanized by cervical dislocation, and left ventricles were collected for RNA isolation. Gene expression in left ventricle was measured by RNA-seq and compared between different time points and chicken lines. The purpose of this study is to investigate gene expression change during broiler cardiac development and to compared gene expression between fast-growing modern broilers and slow-growing heritage broilers to find possible genes and pathways related to differential cardiac development and differential susceptibility to cardiac diseases between the two broiler lines.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Specimen part, Disease

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accession-icon SRP152925
Gallus gallus gallus Transcriptome or Gene expression
  • organism-icon Gallus gallus
  • sample-icon 8 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

broilers heat stress.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Age, Specimen part

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accession-icon SRP064897
lung tissue of pigs Transcriptome or Gene expression
  • organism-icon Sus scrofa
  • sample-icon 4 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

the mRNA expression of pig lung tissue. there are four groups: LW pigs infected with PCV2, LW pigs control, Yorkshire × Landrace (YL) pigs infected with PCV2, Yorkshire × Landrace (YL) pigs control.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Age, Specimen part, Disease, Disease stage, Cell line, Treatment

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accession-icon SRP090540
Danio rerio strain:AB Raw sequence reads
  • organism-icon Danio rerio
  • sample-icon 1 Downloadable Sample
  • Technology Badge IconIlluminaHiSeq4000

Description

Identification of circular RNAs in zebrafish

Publication Title

Identification and characterization of circular RNAs in zebrafish.

Sample Metadata Fields

No sample metadata fields

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accession-icon ERP002075
RNAseq sequencing of 5 unrelated individuals to study RNA-DNA Differences in Human Mitochondria Restore Ancestral Form of 16S Ribosomal RNA
  • organism-icon Homo sapiens
  • sample-icon 5 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2000

Description

RNA sequences are generally identical to the underlying DNA sequences but there are known exceptions. These RNA-DNA differences (RDDs) have been found in the nuclear genomes of human cells and in the mitochondria of plants and animals but not in human mitochondria. Here by deep sequencing of DNA and RNA of human mitochondria, we identified 3 RDD sites including an A-to-U and an A-to-G RDD at position 2617. Examination of the precursor polycistronic mitochondrial transcripts shows that the RDD formation occurs post-transcriptionally. Phylogenetic analysis shows that the ancestral allele at position 2617 was a thymine or a guanine. Thus the RDD formation recapitulates the ancestral form of 16S rRNA. Our findings show that RDD formation like other RNA processing steps is conserved across species and likely has functional significance.

Publication Title

No associated publication

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP015012
Gallus gallus Oviduct Transcriptome
  • organism-icon Gallus gallus
  • sample-icon 6 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

Using HiSeq2000 to sequence white leghorn different parts (ovary, magnum, isthmus and uterus) of oviduct at 40-weeks.

Publication Title

No associated publication

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP063481
RNA-Seq analysis for drip loss in Pietrain × Duroc × Landrace × Yorkshire
  • organism-icon Sus scrofa
  • sample-icon 2 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

Identification of candidate genes for drip loss

Publication Title

No associated publication

Sample Metadata Fields

Sex, Specimen part

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accession-icon SRP092882
Drosophila allele specific expression
  • organism-icon Drosophila melanogaster
  • sample-icon 66 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

This study crossed Drosophila melanogaster genotypes from four populations to the reference genome line. RNAseq data was then generated to study natural variation in allele specific expression.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Specimen part, Cell line

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accession-icon SRP092744
Genes and polymorphism identification associated to hernias in swine
  • organism-icon Sus scrofa
  • sample-icon 8 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Transcriptome of connective tissue of swine affected and non-affected with scrotal hernia

Publication Title

No associated publication

Sample Metadata Fields

Sex, Age, Specimen part, Disease

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refine.bio is a repository of uniformly processed and normalized, ready-to-use transcriptome data from publicly available sources. refine.bio is a project of the Childhood Cancer Data Lab (CCDL)

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Developed by the Childhood Cancer Data Lab

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Cite refine.bio

Casey S. Greene, Dongbo Hu, Richard W. W. Jones, Stephanie Liu, David S. Mejia, Rob Patro, Stephen R. Piccolo, Ariel Rodriguez Romero, Hirak Sarkar, Candace L. Savonen, Jaclyn N. Taroni, William E. Vauclain, Deepashree Venkatesh Prasad, Kurt G. Wheeler. refine.bio: a resource of uniformly processed publicly available gene expression datasets.
URL: https://www.refine.bio

Note that the contributor list is in alphabetical order as we prepare a manuscript for submission.

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