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Robert Nicholls - Research in genetic disease, especially Prader-Willi syndrome; genomic imprinting; transcriptional regulation; animal models; molecular evolution.
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Robert Nicholls

Research in genetic disease, especially Prader-Willi syndrome; genomic imprinting; transcriptional regulation; animal models; molecular evolution.
University of Pittsburgh Medical Center • Children's Hospital of Pittsburgh • Pittsburgh • United States of America

Skills and expertise

Fields of interest
  • Genome edition
  • RNA-seq analysis
  • DNA methylation array analysis
Languages
  • English
Programming languages
  • Other

Fields of interest

Genome edition
Performs analysis, visualization and comparison of sequencing data from genome…
Serves as a calculation and visualization tool for high-throughput CRISPR…
Processes batch analysis of CRISPR edits using Sanger data. ICE can quantify…
RNA-seq analysis
Allows users to browse and visualize multi-omics datasets. WIlsON proposes a…
Assists users in studying allele-specific expression (ASE) within individual…
Provides a platform to build reproducible and flexible pipelines for scalable…
DNA methylation array analysis
Allows to rank, filter and explore cancer genomics data (genes, cell lines and…
Enables to build custom genome browsers. GIVe is a programming library allowing…
Performs secure analyses and visualization of users’ private functional…