Published December 8, 2016 | Version v1
Dataset Open

Training material for ChIP-seq analysis

  • 1. Johns Hopkins University

Description

The data provided here are part of a Galaxy tutorial that analyzes ChIP-seq data from a study published by Wu et al., 2014 (DOI:10.1101/gr.164830.113). The goal of this study was to investigate "the dynamics of occupancy and the role in gene regulation of the transcription factor Tal1, a critical regulator of hematopoiesis, at multiple stages of hematopoietic differentiation." To this end, ChIP-seq experiments were performed in multiple mouse cell types including a G1E cell line and megakaryocytes, the two cell types represented here. The dataset contains biological replicate Tal1 ChIP-seq and input control experiments (*.fastqsanger files). Because of the long processing time for the large original files, we have downsampled the original raw data files to include only reads that align to chromosome 19 and a subset of interesting genomic loci (ChIPseq_regions_of_interest_v4.bed) pulled from the Wu et al. publication. Also included is a gene annotation file (RefSeq_gene_annotations_mm10.bed) with gene names added for viewing in a genome browser.

Files

Files (1.8 GB)

Name Size Download all
md5:0be4221c31ab250558e66c907a093a0d
855 Bytes Download
md5:17abaac1b7c39835cd79d48112aa6c21
36.3 MB Download
md5:e0092c39ec1a8fc58b113398241349f9
433.8 MB Download
md5:abe2705a2d1237f93696aa5af4ec1106
32.8 MB Download
md5:dc695e620b83496520d8a0771f277851
63.6 MB Download
md5:963f7c5eac82c903e4a081470db7b633
59.2 MB Download
md5:1913b19722407118f1a07b5772e99547
411.1 MB Download
md5:5b39bcfc0d6c188a237715ed6225b48e
350.7 MB Download
md5:e24ff5be53e25198fe8615668f85ff1c
371.0 MB Download
md5:ed0d87ba5e3ce3c5cae5f156f52f3f3e
5.1 MB Download

Additional details

References

  • Afgan, E et al. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update. 44, W3–W10 (2016).
  • Wu, W et al. Dynamic shifts in occupancy by TAL1 are guided by GATA factors and drive large-scale reprogramming of gene expression during hematopoiesis. 24, 1945–1962 (2014).