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Status |
Public on Aug 14, 2018 |
Title |
WT H3K27me2/3 ChIPseq |
Sample type |
SRA |
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Source name |
germinated conidia
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Organism |
Neurospora crassa |
Characteristics |
cell type: conidium
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Extracted molecule |
genomic DNA |
Extraction protocol |
none provided by the submitter
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina NextSeq 500 |
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Data processing |
ChIP-seq processing: All sequencing reads were mapped to the corrected N. crassa OR74A (NC12 genome) (Galazka et al., 2016) using Bowtie2 (Langmead and Salzberg, 2012). ChIP-seq read coverage was averaged, normalized, and analyzed using tools available from deepTools2 on the open-source platform Galaxy (Afgan et al., 2016). Sequencing tracks are displayed as 25-nt-window TDF or bigWig files with the Integrative Genomics Viewer (IGV) (Robinson et al., 2011). Genome_build: Neurospora crassa assembly 12 Fixed (files: neurospora_crassa_or74a_12_genome_FIXED.fasta, and neurospora_crassa_or74a_12_transcripts_FIXED.gtf; files are found in GEO submission GSE71024) Supplementary_files_format_and_content: For ChIP-seq files: The tdf files were generated using the "count" function in igvtools (Integrative Genomics Viewer; Broad Institute, Robinson et al, 2011) and bigwig files were generated using DeepTools (Ramirez et al., 2016) using a window size of 20 -200bp (tdf and bigwig files are binary files that shows enrichment peaks for each ChIP sample and have been processed for faster display of the data in IGV). Supplementary_files_format_and_content: For Poly-A mRNA files: Text files contain counts for every gene as outlined in process above.
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Submission date |
Aug 13, 2018 |
Last update date |
Aug 14, 2018 |
Contact name |
Vincent T Bicocca |
E-mail(s) |
bicocca@uoregon.edu
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Organization name |
University of Oregon
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Department |
Biology
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Lab |
Selker
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Street address |
1229 University of Oregon
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City |
Eugene |
State/province |
OR |
ZIP/Postal code |
97403 |
Country |
USA |
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Platform ID |
GPL20660 |
Series (1) |
GSE118495 |
ASH-1-catalyzed H3K36 methylation drives gene repression and marks H3K27me2/3-competent chromatin |
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Relations |
BioSample |
SAMN09828199 |
SRA |
SRX4549856 |
Supplementary file |
Size |
Download |
File type/resource |
GSM3330990_AAAGCA_N3753_K27me2-3_ChIP_S18_R1_001_25.tdf |
10.4 Mb |
(ftp)(http) |
TDF |
GSM3330990_Galaxy149-K27me2.3_MARKED_8.6__of_genes_.bed.bed.gz |
10.2 Kb |
(ftp)(http) |
BED |
GSM3330990_H3K27me2me3_wt_GCCAAT_051515_s.tdf |
4.3 Mb |
(ftp)(http) |
TDF |
GSM3330990_WT_H3K27me2_3_merged_replicates.bigwig |
11.1 Mb |
(ftp)(http) |
BIGWIG |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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