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Links from GEO DataSets

Items: 12

1.

Haloperidol response across genetic backgrounds

(Submitter supplied) We performed short-term bi-directional selective breeding for haloperidol-induced catalepsy, starting from three mouse populations of increasingly complex genetic structure: an F2 intercross, a heterogeneous stock (HS) formed by crossing four inbred strains (HS4) and a heterogeneous stock (HS-CC) formed from the inbred strain founders of the Collaborative Cross (CC). All three selections were successful, with large differences in haloperidol response emerging within three generations. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
275 Samples
Download data
Series
Accession:
GSE37755
ID:
200037755
2.

Selection for Drinking in the Dark Alters Brain Gene Coexpression Networks

(Submitter supplied) Heterogeneous stock (HS/NPT) mice have been used to create lines selectively bred in replicate for elevated drinking in the dark (DID). Both selected lines routinely reach a blood ethanol (EtOH) concentration (BEC) of 1.00 mg/ml or greater at the end of the 4-hour period of access in Day 2. The mechanisms through which genetic differences influence DID are currently unclear. Therefore, the current study examines the transcriptome, the first stage at which genetic variability affects neurobiology. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
134 Samples
Download data: IDAT, TXT
Series
Accession:
GSE93515
ID:
200093515
3.

Allelic imbalance is a prevalent and tissue-specific feature of the mouse transcriptome

(Submitter supplied) We perform a systematic classification of allelic imbalance in mouse hybrids derived from reciprocal crosses of divergent strains. We observe that deviation from balanced biallelic expression is common, occurring in ~20% of the mouse transcriptome. Allelic imbalance attributed to genotype is by far the most prevalent class and typically is tissue-specific. However, some genotype-based imbalance is maintained across tissues and is associated with greater genetic variation, especially in 5’ and 3’ termini of transcripts. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL13112
11 Samples
Download data: BW
Series
Accession:
GSE58524
ID:
200058524
4.

Defining the consequences of genetic variation on a proteome-wide scale

(Submitter supplied) Genetic variation governs protein expression through both transcriptional and post-transcriptional processes. To investigate this relationship, we combined a multiplexed, mass spectrometry-based method for protein quantification with an emerging mouse model harboring extensive genetic variation from 8 founder strains. We collected genome-wide mRNA and protein profiling measurements to link genetic variation to protein expression differences in livers from 192 Diversity Outcross mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
384 Samples
Download data: TXT
Series
Accession:
GSE72759
ID:
200072759
5.

RNA-seq alignment to individualized genomes

(Submitter supplied) The source of most errors in RNA sequencing (RNA-seq) read alignment is in the repetitive structure of the genome and not with the alignment algorithm. Genetic variation away from the reference sequence exacerbates this problem causing reads to be assigned to the wrong location. We developed a method, implemented as the software package Seqnature, to construct the imputed genomes of individuals (individualized genomes) of experimental model organisms including inbred mouse strains and genetically unique outbred animals. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
1086 Samples
Download data: TXT
Series
Accession:
GSE45684
ID:
200045684
6.

Genetic variability of transcript abundance in pig peri-mortem skeletal muscle: eQTL localized genes involved in stress response, cell death, muscle disorders and metabolism.

(Submitter supplied) BACKGROUND: The genetics of transcript-level variation is an exciting field that has recently given rise to many studies. Genetical genomics studies have mainly focused on cell lines, blood cells or adipose tissues, from human clinical samples or mice inbred lines. Few eQTL studies have focused on animal tissues sampled from outbred populations to reflect natural genetic variation of gene expression levels in animals. more...
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL3729
57 Samples
Download data: TXT
Series
Accession:
GSE26924
ID:
200026924
7.

Expression profiling of liver tissue from (C57BL/6J X C3H/HeJ)F2 mice on ApoE null backgrounds

(Submitter supplied) The (C57BL/6J X C3H/HeJ)F2 intercross consists of 334 animals of both sexes. All are ApoE null and received a high fat Western diet from 8-24 weeks of age.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2510
311 Samples
Download data
Series
Accession:
GSE2814
ID:
200002814
8.

Amygdalae and hippocampi of C57BL/6J and A/J mouse inbred strains

(Submitter supplied) Gene expression profiling in C57BL/6J and A/J mouse inbred strains reveals gene networks specific for brain regions independent of genetic background Comparison of whole genome expression data of amygdala and hippocampus of both C57BL/6J and A/J mouse inbred strains using a network approach
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6103
35 Samples
Download data: TXT
Series
Accession:
GSE17955
ID:
200017955
9.

Athero-susceptibility of inbred mouse strains

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL16570 GPL17400
20 Samples
Download data: CEL, CHP
Series
Accession:
GSE53006
ID:
200053006
10.

Expression data from the aorta of DBA, B6 and 129 mice

(Submitter supplied) Strain differences influence susceptibility to atherosclerosis. Apolipoprotein E-null mice on a DBA/2J genetic background (DBA-apoE) and C57BL/6 (B6-apoe) are highly susceptible to atherosclerosis in the aortic root area compared with those on a 129S6/SvEvTac background (129-apoE). To explore strain-specific differences affecting the susceptibility to atherosclerosis, we performed microarray analysis of aortic arch and root from wild type mice of each strains.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE52818
ID:
200052818
11.

Expression data from thioglycollate-elicited peritoneal macrophages from 129S6/SvEvTac and C57BL/6 mice

(Submitter supplied) Strain differences influence susceptibility to atherosclerosis. Apolipoprotein E-null mice on a C57BL/6 genetic background (B6-apoE) are highly susceptible to atherosclerosis in the aortic root area compared with those on a 129S6/SvEvTac background (129-apoE). To explore strain-specific differences affecting the susceptibility to atherosclerosis, we performed microarray analysis of macrophages from wild type mice of each strains.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE52816
ID:
200052816
12.

Expression data from thioglycollate-elicited peritoneal macrophages from 129S6/SvEvTac and DBA2/J mice

(Submitter supplied) Strain differences influence susceptibility to atherosclerosis. Apolipoprotein E-null mice on a DBA/2J genetic background (DBA-apoE) are highly susceptible to atherosclerosis in the aortic root area compared with those on a 129S6/SvEvTac background (129-apoE). To explore strain-specific differences affecting the susceptibility to atherosclerosis, we performed microarray analysis of macrophages from wild type mice of each strains.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE52473
ID:
200052473
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