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Items: 4

1.

Shared transcriptional profiles at the single cell level of atypical memory B cells suggest common drivers of expansion and function in malaria, HIV and autoimmune diseases [Malaria VDJ+GEX scRNA-seq]

(Submitter supplied) Human chronic infectious diseases have been shown to alter the composition and phenotype of the B cell compartment, which, in part, can attribute to failure to acquire protective immunity. However, the extent of such alterations is poorly understood. Here, using a combination of bulk and single cell RNA-sequencing (scRNA-seq) of B cells in individuals living in malaria-endemic Africa, we characterized changes in naïve B cell, classical memory B cell (MBC) and atypical MBC subsets. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL21290
2 Samples
Download data: CSV, TSV
Series
Accession:
GSE157967
ID:
200157967
2.

Chronic Malaria drives functional heterogenity in B cell subpopilations and expansion of unswitched atypical memory B cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
4 related Platforms
23 Samples
Download data: CSV, TSV
Series
Accession:
GSE149729
ID:
200149729
3.

Illumina HiSeq 3000 (Homo sapiens)

Platform
Accession:
GPL21290
ID:
100021290
4.

Mal_Subject 1_VDJ+GEX scRNA-seq

Organism:
Homo sapiens
Source name:
Peripheral mononuclear blood cells (PBMCs)
Platform:
GPL21290
Series:
GSE149729 GSE157967
Download data: CSV
Sample
Accession:
GSM4782043
ID:
304782043
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db=gds|term=GSM4782043[Accession]|query=1|qty=2|blobid=MCID_674c39d996d9ad0406222181|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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