Dataset
Systematic comparative analysis of single-nucleotide variant detection methods from single-cell RNA sequencing data
Dataset ID | Technology | Samples |
---|---|---|
EGAD00001005373 | Illumina HiSeq 4000 | 75 |
Dataset Description
We generated SMART-seq2 data for 70 CD45- single cells, which were derived from two colorectal cancer patients (P0411 and P0413). The average sequencing depths of these cells were 1.4 million reads per cell. We also generated tumor and adjacent normal bulk WES data, as well as tumor bulk RNA-seq data for these patients.
Data Use Conditions
RUO PUB US IS HMB
See further information on Data Use Conditions
Label | Code | Version | Modifier |
---|---|---|---|
obsolete research use only | DUO:0000014 | 2019-01-07 | |
publication required | DUO:0000019 | 2019-01-07 | |
user specific restriction | DUO:0000026 | 2019-01-07 | |
institution specific restriction | DUO:0000028 | 2019-01-07 | |
health or medical or biomedical research | DUO:0000006 | 2019-01-07 |