Long noncoding ribonucleic acids (lncRNAs) are transcripts greater than 500 nucleotides in length that do not encode for protein. Through their sequences and structures, lncRNAs interact with other nucleic acids and proteins to regulate a variety of biological processes, including gene expression. The rate at which lncRNAs have been identified exceeds our ability to study their structures and functions. Within the last decade, several tens of thousands have been discovered throughout the human genome, yet fewer than 50 have been structurally characterized. In an attempt to better understand and map the vast molecular networks that underlie biological activity, several genome-wide studies have been carried out to study RNA structures, identify their cognate protein binding partners, and map sites of protein binding. Every class of RNA is represented in these studies, including lncRNAs. In this study, we mined this data to investigate the propensity of X-inactivation (XCI) escaping lncRNAs to interact with the RNA binding protein (RBP) RBM15. We find that XCI-escaping lncRNAs are intricately structured and, depending on their localization (cytoplasm, nucleoplasm, chromatin), adopt different structures. Bioinformatic and experimental analyses reveal that U-containing sequences are bound by RNA recognition motifs (RRMs) 2 and 3 of RBM15. Collectively, the mining of data, carried out by graduate students of the New York University Spring 2023 Macromolecular Chemistry course, and the experimental validation of those results, carried out by high school summer interns from traditionally excluded groups, demonstrates i) an efficient way to make use of the genome-wide studies that have been carried out to better understand how lncRNAs function and ii) a way to engage students from a variety of backgrounds in biological research.