|
Status |
Public on Mar 27, 2017 |
Title |
K36R Start-seq mixed NextSeq rep1 |
Sample type |
SRA |
|
|
Source name |
Whole 3rd Instar Larvae
|
Organism |
Drosophila melanogaster |
Characteristics |
developmental stage: 3rd instar larvae tissue: Whole larvae Sex: Mixed genotype: K36R target molecule: Short nascent capped RNA
|
Growth protocol |
3rd instar larvae were staged by wandering behavior and collected for extraction
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from isolated nuclei using TRIzol reagent (Thermo Fisher) using manufacturer's protocols. Start-seq libraries were prepared as previously described (Henriques et al., 2013; Nechaev et al., 2010).
|
|
|
Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
HWT vs. K36R Start-seq processed file: obsTSS_calls.full.bed processed file: nuTSS_calls.full.header.bed
|
Data processing |
Library strategy: Start-seq (Nechaev et al. 2010, Henriques et al. 2013) Alignment to reference genome using Tophat2 (RNA-seq) or Bowtie2 (Start-seq, ATAC-seq) Generation of count tables for RNA-seq using htseq-count Differential expression analysis of RNA-seq using DESeq2 or Cufflinks Assignment of nucleotide position for Start-seq peaks using custom scripts Generation of BigWig files for ATAC-seq samples using Deeptools Analysis of meta-TSS profiles for ATAC-seq samples using Deeptools Genome_build: dm3
|
|
|
Submission date |
Mar 22, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Michael Meers |
E-mail(s) |
[email protected]
|
Organization name |
UNC Chapel Hill
|
Street address |
250 Bell Tower Dr.
|
City |
Chapel Hill |
State/province |
NC |
ZIP/Postal code |
27599 |
Country |
USA |
|
|
Platform ID |
GPL19132 |
Series (1) |
GSE96922 |
Histone gene replacement reveals a post-transcriptional role for H3K36 in maintaining metazoan transcriptome fidelity |
|
Relations |
BioSample |
SAMN06627565 |
SRA |
SRX2661669 |