Scientific Data · 2020 · 41 citations · 19 references
MedicineNeurologyOncologyGenomicsNeuro-oncologyTranscriptomicsCancer GenomicsCancer TranscriptomicsMolecular Tumor ProfilingNeuro-oncologic PathologyPeripheral Nerve TumorsTranscriptomic ProfilingCancer BioinformaticsCancer Genomics DatabasesClinical Text AnnotationNerve Sheath Tumor PathologyNeurofibromatosis Type 1Neurologic DeficitsPeripheral Nerve Tumor Genetic ProfilingPeripheral Nerve Tumor Histopathology
Nerve sheath tumors occur as a heterogeneous group of neoplasms in patients with neurofibromatosis type 1 (NF1). The malignant form represents the most common cause of death in people with NF1, and even when benign, these tumors can result in significant disfigurement, neurologic dysfunction, and a range of profound symptoms. Lack of human tissue across the peripheral nerve tumors common in NF1 has been a major limitation in the development of new therapies. To address this unmet need, we have created an annotated collection of patient tumor samples, patient-derived cell lines, and patient-derived xenografts, and carried out high-throughput genomic and transcriptomic characterization to serve as a resource for further biologic and preclinical therapeutic studies. In this work, we release genomic and transcriptomic datasets comprised of 55 tumor samples derived from 23 individuals, complete with clinical annotation. All data are publicly available through the NF Data Portal and at http://synapse.org/jhubiobank.
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The Sequence Alignment/Map format and SAMtools
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Salmon provides fast and bias-aware quantification of transcript expression
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