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Genome-wide promoter methylation analysis in neuroblastoma identifies prognostic methylation biomarkers
Authors:Anneleen Decock  Maté Ongenaert  Jasmien Hoebeeck  Katleen De Preter  Gert Van Peer  Wim Van Criekinge  Ruth Ladenstein  Johannes H Schulte  Rosa Noguera  Raymond L Stallings  An Van Damme  Geneviève Laureys  Joëlle Vermeulen  Tom Van Maerken  Frank Speleman  Jo Vandesompele
Institution:1. Institute for Human Genetics, UCSF, 513 Parnassus Avenue, Box 0794, San Francisco, CA, 94143-0794, USA
2. The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, UCSF, 35 Medical Center Way, San Francisco, CA, 94143-0525, USA
3. Department of Epidemiology and Biostatistics, UCSF, 185 Berry Street, Lobby 5, Suite 5700, San Francisco, CA, 94107, USA
4. Department of Bioengineering and Therapeutic Sciences, UCSF, 513 Parnassus Avenue, San Francisco, CA, 94143-0912, USA
Abstract:ChIP-seq is a powerful method for obtaining genome-wide maps of protein-DNA interactions and epigenetic modifications. CHANCE (CHip-seq ANalytics and Confidence Estimation) is a standalone package for ChIP-seq quality control and protocol optimization. Our user-friendly graphical software quickly estimates the strength and quality of immunoprecipitations, identifies biases, compares the user's data with ENCODE's large collection of published datasets, performs multi-sample normalization, checks against quantitative PCR-validated control regions, and produces informative graphical reports. CHANCE is available at https://github.com/songlab/chance.
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