Our kits take you from single cell or single nuclei suspensions through sequencing straight into biological insights.
Target 100s to 1000s of genes to analyze more samples with less sequencing.
Pair guide RNAs with single cell whole transcriptomes.
Transform single cell sequencing output into understandable results.
Parse Biosciences provides researchers with the ability to perform single cell sequencing with unprecedented scale and ease.
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Bone marrow mononuclear cells were obtained from four control (D3, D5, D6, and D7), three acute myeloid leukemia (D1, D2, and D4), and one acute lymphocytic leukemia (D8). The leukemia samples came from recently diagnosed donors that had not received treatments prior to collection. The samples were fixed with Evercode Cell Fixation. Equal number of cells from all eight donors were used as input into the Evercode WT Mega v2 kit. One sublibrary was sequenced on an Illumina NextSeq 550, and data was processed with Parse Biosciences Analysis Pipeline v1.0.1a.
You can explore the data and do your own analysis by downloading the raw data below.
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Experimental Summary Reports, Digital Gene Expression (DGE) Matrix, All Gene, and Cell Metadata for Evercode WT v2.
Experimental Summary Report (HTML) Digital Gene Expression (DGE) Matrix (549 MB) All Gene (CSV) Cell Metadata (CSV)