Project description:The data contained in this experiment correspond to Illumina-based whole genome shotgun sequencing of the Personal Genomes Project 1 donor (PGP1) donor ENCDO336AAA. They were made using a PCR-based (9-cycle, ENCLB234AQO) protocol sequenced on multiple lanes to a combined depth of ~ 60X in PE125 format. For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_Data_Use_Policy_for_External_Users_03-07-14.pdf
Project description:This dataset contains spatial transcriptomics data of four lung neuroendocrine tumours (lung NETs), a rare and understudied type of lung cancer. The dataset consists of raw sequencing data, metadata, and gene expression matrices. It is part of the lungNENomics project. See https://doi.org/10.5281/zenodo.19366762 for processed data for the series, including downstream analyses data for the four samples in this dataset, such as inferred CNVs and aneuploidy status, and spatial domain and cell proportions for each spot. The lungNENomics project also generated other molecular data for a series of more than 200 samples. The raw sequencing data (fastq files for RNA-seq, cram files for WGS, and idat files for methylation arrays) is hosted on the European Genome-Phenome Archive website, study EGAS00001005979. Medical imaging data (Hematoxylin & Eosin stained whole-slide images) from the lungNENomics project is hosted in the EBI bioImage Archive (10.6019/S-BIAD3143).
Project description:Temporal analysis of Irf4 and PU.1 genome binding during B cell activation and differentiation in vitro using antigen (NP-Ficoll) CD40L and IL-2/4/5 cytokines (see Molecular Systems Biology 7:495 for details of cellular system). The results provide insight in the target genes and binding specificity of IRF4 and PU.1 during coordination of different programs of B cell differentiation. Regrettably three of the FASTQ raw sequence files in our study were corrupted during storage. FASTQ data from our experimental and control groups are available for download via GEO SRA; however, two groups are missing select raw sequence files. These include one PU.1 Day 3 group file (Sample GSM1133499) and two of four input files used to generate a concatenated “super” input file (Sample GSM1133490); the raw data provided for input consists of the two input files recovered. Importantly, FASTA sequences for both of these datasets are available as supplementary data through GEO, and we can make available upon request (rsciamma@uchicago.edu) all files in our study in the ELAND-extended alignment format. Please note that GEO no longer supports this format.
Project description:20 random DNA barcodes were designed in silico and transfected into PC3 cells. Barcodes were sequenced using Illumina-Miseq technology to find the sequence and their respective copy numbers. Current file contains the raw data of these DNA barcodes in fastq format
