|
Status |
Public on Mar 15, 2018 |
Title |
BA40_1503_input |
Sample type |
SRA |
|
|
Source name |
Brodmann area 40
|
Organism |
Homo sapiens |
Characteristics |
cell type: Frozen brain tissue line: -- Sex: M age: 60
|
Treatment protocol |
6μg of rabbit αCLOCK (ab3517, Abcam, lot #GR222742-4) was used for CLOCK ChIP and 6μg of normal rabbit αIgG (#2729, Cell Signaling) was used as a negative control. Please refer to manuscript for detailed ChIP protocol, adapted from Koike et. al. 2012 (PMID: 22936566).
|
Growth protocol |
Differentiated human neural progenitor cells and adult human BA10 and BA40 neocortex was used
|
Extracted molecule |
genomic DNA |
Extraction protocol |
DNA was purified using Qiagen Qiaquick PCR purification kit, assayed for quality by Bioanalyzer (Agilent), and quantified using a Qubit Fluorometer according to the manufacturer’s instructions. Libraries were prepared using previously published methods (PMID: 25662462)
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
Single-end reads were aligned in a staged manner. Reads were aligned with STAR 2.5.2b using options "“--outFilterMultimapNmax 10 --alignSJoverhangMin 10 --alignSJDBoverhangMin 1 --outFilterMismatchNmax 3 --twopassMode Basic" to a reference sequence comprised of mitochondrial DNA (hg38 from UCSC) ChIP-seq data were aligned with STAR 2.5.2b using options "“--outFilterMultimapNmax 10 --alignSJoverhangMin 10 --alignSJDBoverhangMin 1 --outFilterMismatchNmax 3 --twopassMode Basic" to a reference sequence comprised of mitochondrial DNA (hg38 from UCSC). ChIP-seq was analyzed using MACS2 with following parameter "--bw 300 --tsize 50 --nomodel --keep-dup all --extsize 300 -q 0.05 –nolambda". ChIP-seq was analyzed using MACS2 with default parameter and "--nolambda --shift 75". bed-files including coordinates of the detected peaks from ChIP-Seq. Genome_build: Human hg38
|
|
|
Submission date |
Mar 15, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Genevieve Konopka |
E-mail(s) |
gena@alum.mit.edu
|
Organization name |
UT Southwestern Medical Center
|
Department |
Neuroscience
|
Street address |
5323 Harry Hines Blvd.
|
City |
Dallas |
State/province |
TX |
ZIP/Postal code |
75390-9111 |
Country |
USA |
|
|
Platform ID |
GPL18573 |
Series (1) |
GSE96659 |
Novel transcriptional networks regulated by CLOCK in human neurons |
|
Relations |
BioSample |
SAMN06604891 |
SRA |
SRX2642656 |