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Items: 3

1.

Single-cell RNA-seq reveals a distinct transcriptome signature of hematopoiesis in GATA2 deficiency

(Submitter supplied) Background and Purpose: Constitutional GATA2 deficiency caused by heterozygous germline GATA2 mutation has a broad spectrum of clinical phenotypes including systemic infections, lymphedema, cytopenias, MDS and AML. A comprehensive profiling of transcriptome of hematopoiesis in GATA2 deficiency is currently lacking. Methods: We performed single-cell RNA sequencing of sorted bone marrow CD34+ hematopoietic stem and progenitor cells (HSPCs) from eight GATA2 deficiency patients, who had various well characterized GATA2 mutations and clinically manifest myelodysplasia. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
13 Samples
Download data: CSV
Series
Accession:
GSE135194
ID:
200135194
2.

Illumina HiSeq 3000 (Homo sapiens)

Platform
Accession:
GPL21290
ID:
100021290
3.

GATA2 deficiency patient 3

Organism:
Homo sapiens
Source name:
human bone marrow
Platform:
GPL21290
Series:
GSE135194
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Sample
Accession:
GSM3993345
ID:
303993345
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