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ChIP-seq experiments using low numbers of input cells, scaled down to the point where data quality is unnacceptably compromised, reveals limits of the technique. Two-part ChIPseq study using native chromatin (non-crosslinked) generated with MNase from human CD4+ cells. Part 1: Previously published p...
ORGANISM(S): Homo sapiens 
Seq-Well: A portable, low-cost platform for single-cell RNA-seq of low-input samples
We developed a sample preparation method for low-input proteomics using lauryl maltose neopentyl glycol. Using the developed method, we performed proteome analysis of 100ng of HEK293T proteins, coIP samples, and serum extracellular vesicles, and further challenged label-free single-cell proteomics o...
ORGANISM(S): Homo Sapiens (human) Bos Taurus 
In this experiment, we've examined chromatin conformation of OG2 (B6; CBA-Tg(Pou5f1-EGFP)2Mnn/J; stock number 004654) mouse stem cells cultured as described in (Shi et al., 2008), using different amounts of starting cells. We performed a modified in situ Hi-C protocol for 6 samples digested with Mbo...
ORGANISM(S): Mus musculus 
Low-input ATAC-seq of mouse EPCR+ and EPCR– hematopoietic stem cell and multipotent progenitor cell populations
CoBATCH for high-throughput single-cell epigenomic profiling [low input in situ ChIP]
Ultra-low-input native ChIP-seq data of four germ-cell types during mouse spermatogenesis
Evaluation of ultra-low input RNA sequencing for the study of human T cell transcriptome
Cell-free DNA methylome profiling by MBD-seq with ultra-low input
Caenorhabditis elegans is a widely used genetic model organism, however, the worm cuticle complicates extraction of intracellular proteins, a prerequisite for typical bottom-up proteomics. Conventional physical disruption procedures are not only time-consuming, but can also cause significant sample ...
ORGANISM(S): Caenorhabditis Elegans (ncbitaxon:6239) 
2025-01-02 | MSV000096763 | MassIVE
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