|
Status |
Public on May 04, 2023 |
Title |
AML processed with GTAC |
Sample type |
SRA |
|
|
Source name |
bone marrow
|
Organism |
Homo sapiens |
Characteristics |
tissue: bone marrow cell line: primary sample cell type: CD34+
|
Extracted molecule |
genomic DNA |
Extraction protocol |
NGS library preparation and purification GTAC
|
|
|
Library strategy |
ATAC-seq |
Library source |
genomic |
Library selection |
other |
Instrument model |
NextSeq 550 |
|
|
Description |
demultiplexed scATAC-seq data from a GTAC experiment
|
Data processing |
FASTQ files were trimmed and converted to BAM. BAM files were de-duplicated using Picard. De-duplicated BAM files were merged with Samtools and the provided fragment files were generated. Fragment files were used as input for analysis in ArchR. Assembly: hg38 Supplementary files format and content: Fragment files from merged BAM files. Each fragment is linked to the single cell where it derives from.
|
|
|
Submission date |
Oct 04, 2022 |
Last update date |
May 04, 2023 |
Contact name |
Sven Turkalj |
E-mail(s) |
sven.turkalj@kellogg.ox.ac.uk
|
Phone |
07307186118
|
Organization name |
WIMM
|
Department |
Radcliffe Department of Medicine
|
Lab |
Vyas Lab
|
Street address |
John Radcliffe Hospital/Headley Way, Oxford OX3 9DS
|
City |
Oxford |
ZIP/Postal code |
OX3 9DS |
Country |
United Kingdom |
|
|
Platform ID |
GPL21697 |
Series (1) |
GSE214812 |
GTAC enables parallel genotyping of multiple genomic loci with chromatin accessibility profiling in single cells |
|
Relations |
BioSample |
SAMN31155143 |
SRA |
SRX17797471 |