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Validation of dedifferentiated liposarcoma (DDLS) cell lines with the original tumors via copy number alteration analysis [sequencing]
- Authors
- Okada, TomoyoGularte-Mérida, RodrigoShen, YaweiSinger, Samuel
- Description
Summary from GEO: "We validated patient's tumor-derived cell lines of liposarcoma by analysing copy number alterations using aCGH or WGS and comparing with the original tumor tissues." Overall design from GEO: "Examination of copy number alterations for 2 cell lines, one of the original tumor, one PDX-tumor and its original tumor."
- Subject
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Cell Line, TumorDNA Copy Number VariationsLiposarcoma
- Access Rights
- Free to All
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Validation of dedifferentiated liposarcoma (DDLS) cell lines with the original tumors via copy number alteration analysis [array]
- Authors
- Okada, TomoyoGularte-Mérida, RodrigoShen, YaweiSinger, Samuel
- Description
Summary from GEO: "We validated patient's tumor-derived cell lines of liposarcoma by analysing copy number alterations using aCGH or WGS and comparing with the original tumor tissues." Overall design from GEO: "Examination of copy number alterations for 2 cell lines, one of the original tumor, one PDX-tumor and its original tumor."
- Subject
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Cell Line, TumorDNA Copy Number VariationsLiposarcoma
- Access Rights
- Free to All
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Table S6 from Phase II Clinical Trial of Everolimus in a Pan-Cancer Cohort of Patients with mTOR Pathway Alterations
- Authors
- Adib, ElioKlonowska, KatarzynaGiannikou, KrinioDo, Khanh T.15 more author(s)...
- Description
Description from Figshare: "Table S6. Copy number alterations (CNAs) in cancer genes identified by whole exome sequencing (WES) and/or initial panel sequencing. Each sheet is a different tumor sample."
- Subject
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Clinical Trial, Phase IIDNA Copy Number VariationsEverolimusHigh-Throughput Nucleotide SequencingNeoplasms/drug therapyTOR Serine-Threonine Kinases
- Access Rights
- Free to All
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Supplementary Table S1 from Smarca4 Inactivation Promotes Lineage-Specific Transformation and Early Metastatic Features in the Lung
- Authors
- Concepcion, Carla P.Ma, SaiLaFave, Lindsay M.Bhutkar, Arjun19 more author(s)...
- Description
Description from Figshare: "Mutations and copy number alterations in PDX models used in this study"
- Subject
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Adenocarcinoma of LungCell LineageDNA Copy Number VariationsLung NeoplasmsNeoplasm Metastasis
- Access Rights
- Free to All
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Supplementary Table 4 from Next-Generation Sequencing of Pulmonary Large Cell Neuroendocrine Carcinoma Reveals Small Cell Carcinoma–like and Non–Small Cell Carcinoma–like Subsets
- Authors
- Rekhtman, NatashaPietanza, Maria C.Hellmann, Matthew D.Naidoo, Jarushka16 more author(s)...
- Description
Description from Figshare: "Supplementary Table 4: Complete list of mutations and copy number alterations detected by MSK-IMPACT in 45 LCNECs"
- Subject
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Carcinoma, NeuroendocrineCarcinoma, Non-Small-Cell LungDNA Copy Number VariationsLung NeoplasmsMutation/geneticsSmall Cell Lung Carcinoma
- Access Rights
- Free to All
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CoMMpass IA19: Data from "Gene interaction network analysis in multiple myeloma detects complex immune dysregulation associated with shorter survival"
- Description
The Multiple Myeloma Research Foundation (MMRF) runs a multi-site longitudinal clinical registry study of patients newly diagnosed with MM. This project is called CoMMpass, and collects both clinical and genomic information periodically. Researchers used interim analysis 19 (IA19) for their conclusions in "Gene interaction network analysis in multiple myeloma detects complex immune dysregulation...
- Subject
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Clinical TrialDNA Copy Number VariationsGenomicsMultiple MyelomaRNA-SeqWhole Genome Sequencing
- Access Rights
- Free to all with registration
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Code from "Gene interaction network analysis in multiple myeloma detects complex immune dysregulation associated with shorter survival"
- Authors
- Simhal, Anish Kumar
- Description
Code associated with the manuscript for "Gene interaction network analysis in multiple myeloma detects complex immune dysregulation associated with shorter survival." Includes data and instructions, R scripts, lab notebooks, and high resolution images.
- Subject
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DNA Copy Number VariationsMultiple MyelomaRNA-SeqSoftware
- Access Rights
- Free to All
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JaBbA (Junction Balance Analysis)
- Authors
- Imielinski, Marcin
- Description
Description from GitHub: "JaBbA builds a genome graph based on junctions and read depth from whole genome sequencing, inferring optimal copy numbers for both vertices (DNA segments) and edges (bonds between segments). It can be used for discovering various patterns of structural variations. If you use JaBbA in your work, please cite: Distinct Classes of Complex Structural Variation Uncovered across...
- Subject
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DNA Copy Number VariationsGenomicsMutation/geneticsNeoplasms/geneticsWhole Genome Sequencing
- Access Rights
- Free to All