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Items: 1 to 20 of 285

1.

Genome-Scale Exon Perturbation Screens Uncover Critical Exons for Cell Fitness

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; unidentified plasmid
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
5 related Platforms
139 Samples
Download data: BW, PSI, TAB
Series
Accession:
GSE244374
ID:
200244374
2.

Genome-Scale Exon Perturbation Screens Uncover Critical Exons for Cell Fitness [CRISPR]

(Submitter supplied) Although CRISPR-Cas technology has revolutionized functional genomics, the systematic exploration of the role of individual exons for critical cellular phenotypes is lagging, limiting our understanding of genome regulation. To overcome this constraint, we have optimized and applied massively parallel exon deletion and splice site mutation screens in human cell lines identifying thousands of exons required for cell fitness. more...
Organism:
Homo sapiens; unidentified plasmid
Type:
Other
5 related Platforms
85 Samples
Download data: TXT
Series
Accession:
GSE244337
ID:
200244337
3.

Genome-wide screening identifies Trim33 as an essential regulator of dendritic cell differentiation [Hoxb8-FL Brie sgRNA-Seq]

(Submitter supplied) The development of all dendritic cells (DCs) including antigen-presenting conventional DCs (cDCs) and cytokine-producing plasmacytoid DCs (pDCs) is controlled by the growth factor Flt3 ligand (Flt3L) and its receptor Flt3. We genetically dissected this common Flt3L-driven pathway of DCs differentiation using CRISPR/Cas9-based dropout screening in a Flt3L-dependent progenitor cell line. Genome-wide screening identified multiple regulators of DC differentiation including the glycosylphosphatidylinositol transamidase complex and arginine methyltransferase Carm1, whose role was confirmed in vivo. more...
Organism:
Mus musculus; unidentified plasmid
Type:
Other
Platforms:
GPL32254 GPL21103
6 Samples
Download data: CSV
Series
Accession:
GSE202942
ID:
200202942
4.

Genome-wide screening identifies Trim33 as an essential regulator of dendritic cell differentiation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; unidentified plasmid
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
4 related Platforms
38 Samples
Download data: BW
Series
Accession:
GSE202585
ID:
200202585
5.

Nucleosome density shapes kilobase-scale regulation by a mammalian chromatin remodeler

(Submitter supplied) SAMOSA, a method previously developed in the Ramani Lab, was employed to reveal nucleosome patterns from remodeling reactions in vitro with the Imitation Switch (ISWI) ATP-Dependent Remodeler ATPase, SNF2h. SAMOSA was further employed to reveal single-molecule nucleosome patterns in vivo from SNF2h knockout and re-expression murine embryonic stem cells.
Organism:
Mus musculus; unidentified plasmid
Type:
Other
Platforms:
GPL29466 GPL29177
235 Samples
Download data: PICKLE
Series
Accession:
GSE197979
ID:
200197979
6.

GO-CRISPR: a highly controlled workflow to improve discovery of gene essentiality

(Submitter supplied) Genome-wide CRISPR screens aid researchers in discovering genes that function across a broad range of cellular mechanisms. Loss-of-function screens are particularly useful for identifying essential genes through loss of cell fitness measurements. However, loss-of-function screens are more challenging compared to gain-of-function screens due to the limited dynamic range of decreased sgRNA sequence detection. more...
Organism:
Homo sapiens; unidentified plasmid
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21697 GPL28513
13 Samples
Download data: CSV
Series
Accession:
GSE150246
ID:
200150246
7.

satmut_utils: a simulation and variant calling package for multiplexed assays of variant effect

(Submitter supplied) We use stable expression of a cystathionine-beta synthase (CBS) variant library in HEK293T cells to identify CBS coding sequence variants that alter mRNA abundance
Organism:
unidentified plasmid; Homo sapiens
Type:
Other
6 related Platforms
22 Samples
Download data: TXT
Series
Accession:
GSE201057
ID:
200201057
8.

Quantitative-enhancer-FACS-seq (QeFS) reveals epistatic interactions among motifs within transcriptional enhancers in developing Drosophila tissue

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster; unidentified plasmid
Type:
Other
Platforms:
GPL21376 GPL19132
19 Samples
Download data: FASTA, TSV, TXT
Series
Accession:
GSE149908
ID:
200149908
9.

Quantitative-enhancer-FACS-seq (QeFS) reveals epistatic interactions among motifs within transcriptional enhancers in developing Drosophila tissue [plasmid]

(Submitter supplied) Activity of enhancers in Drosophila embryos was measured by highly parallel reporter assay. We examined the results of mutating binding sites for 4 poorly studied TFs individually or in combination, and characterized complex genetic interactions among the different classes of motif mutant.
Organism:
unidentified plasmid
Type:
Other
Platform:
GPL21376
1 Sample
Download data: FASTA, TSV, TXT
Series
Accession:
GSE149875
ID:
200149875
10.

Rewiring of human neurodevelopmental gene regulatory programs by Human Accelerated Regions (HARs)

(Submitter supplied) Human Accelerated Regions (HARs) are the fastest-evolving regions of the human genome and many are hypothesized to function as regulatory elements that drive human-specific gene regulatory programs. We interrogate the in vitro enhancer activity of >3,100 HARs in massively parallel reporter assays (MPRAs), demonstrating that many HARs appear to act as neural enhancers and that sequence divergence at HARs has largely augmented their neuronal enhancer activity.
Organism:
Homo sapiens; Mus musculus; unidentified plasmid
Type:
Other
Platforms:
GPL30428 GPL21273 GPL20795
14 Samples
Download data: BED, TXT
Series
Accession:
GSE180714
ID:
200180714
11.

Benchmarking of SpCas9 variants enables deeper base editor screens of BRCA1 and BCL2

(Submitter supplied) Numerous rationally-designed and directed-evolution variants of SpCas9 have been reported to expand the utility of CRISPR technology. Here, we benchmark PAM preferences, on-target activity, and off-target susceptibility of 11 variants of SpCas9 in cell culture assays with thousands of guides targeting endogenous genes. To enhance the coverage and thus utility of base editing screens, we demonstrate that the SpCas9-NG and SpG variants are compatible with both A>G and C>T base editors, more than tripling the number of guides and assayable residues. more...
Organism:
unidentified plasmid; Homo sapiens
Type:
Other
Platforms:
GPL25362 GPL16791
67 Samples
Download data: XLSX
Series
Accession:
GSE180351
ID:
200180351
12.

CRISPR activation and interference screens decode stimulation responses in primary human T cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
unidentified plasmid; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL28010 GPL18573
68 Samples
Download data
Series
Accession:
GSE174292
ID:
200174292
13.

CRISPR activation and interference screens decode stimulation responses in primary human T cells [CRISPR]

(Submitter supplied) Regulation of cytokine production in stimulated T cells can be disrupted in autoimmunity, immunodeficiencies, and cancer. Systematic discovery of stimulation-dependent cytokine regulators requires both loss-of-function and gain-of-function studies, which have been challenging in primary human cells. We now report genome-wide CRISPR activation (CRISPRa) and interference (CRISPRi) screens in primary human T cells to identify gene networks controlling interleukin 2 and interferon gamma production. more...
Organism:
Homo sapiens; unidentified plasmid
Type:
Other
Platforms:
GPL18573 GPL28010
52 Samples
Download data: XLSX
Series
Accession:
GSE174255
ID:
200174255
14.

Barcoded viral tracing of single-cell interactions in CNS inflammation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; unidentified plasmid; Suid alphaherpesvirus 1
Type:
Other; Expression profiling by high throughput sequencing
6 related Platforms
128 Samples
Download data: CSV, TAR, TSV, TXT, ZIP
Series
Accession:
GSE150858
ID:
200150858
15.

Analysis of diversity in barcoded plasmid library

(Submitter supplied) Validating plasmid barcode diversity
Organism:
unidentified plasmid
Type:
Other
Platform:
GPL28010
1 Sample
Download data: TXT
Series
Accession:
GSE149994
ID:
200149994
16.

Global discovery of SLE genetic risk variant allelic enhancer activity

(Submitter supplied) Genome-wide association studies of Systemic Lupus Erythematosus (SLE) nominate 3,073 genetic variants at 91 risk loci. To systematically screen these variants for allelic transcriptional enhancer activity, we constructed a massively parallel reporter assays (MPRA) library comprising 12,396 DNA oligonucleotides containing the genomic context around every allele of each SLE variant. Transfection into Epstein-Barr virus-transformed B cell line GM12878 revealed 482 variants with enhancer activity, with 51 variants showing genotype-dependent (allelic) enhancer activity at 27 risk loci. more...
Organism:
unidentified plasmid; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL28010 GPL24676 GPL18573
25 Samples
Download data: TXT, XLSX
Series
Accession:
GSE143792
ID:
200143792
17.

Massively multiplex single-molecule oligonucleosome footprinting

(Submitter supplied) SAMOSA is a single-molecule oligonucleosome footprinting technology, which can be employed to reveal nucleosome patterns (nucleosome positioning, nucleosome repeat length) at transcription factor binding sites and epigenomic domains.
Organism:
unidentified plasmid; Homo sapiens
Type:
Other
Platforms:
GPL29466 GPL28352 GPL29465
22 Samples
Download data: NPY, PICKLE
Series
Accession:
GSE162410
ID:
200162410
18.

Genome-wide CRISPR screen of rituximab induced cell depletion

(Submitter supplied) We screened the genome of OCI-Ly-7, a Diffuse Large B-cell Lymphoma cell line, for genes mediating the response to rituximab treatment. We utilized the genome-wide library GeCKO v2 (A+B) from Feng Zhang. (Addgene#1000000049)
Organism:
Homo sapiens; unidentified plasmid
Type:
Other
Platforms:
GPL23227 GPL27656
5 Samples
Download data: TXT
Series
Accession:
GSE139385
ID:
200139385
19.

Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; unidentified plasmid
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
5 related Platforms
210 Samples
Download data: BED, BW
Series
Accession:
GSE136703
ID:
200136703
20.

Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits [MPRA]

(Submitter supplied) Genome-wide association studies have associated thousands of genetic variants with complex traits and diseases, but pinpointing the causal variant(s) among those in tight linkage disequilibrium with each associated variant remains a major challenge. Here, we used seven experimental assays to characterize all common variants at the multiple disease-associated TNFAIP3 locus in three disease-relevant immune cell types, based on a set of features related to regulatory potential. more...
Organism:
Homo sapiens; unidentified plasmid
Type:
Other
Platforms:
GPL25362 GPL24676 GPL16791
33 Samples
Download data: FASTA, MAP, TXT
Series
Accession:
GSE136702
ID:
200136702
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