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TranscriptomicsIntegrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma [methylation]
Osteosarcomas are the most common primary malignant tumours of bone, and almost all conventional osteosarcomas are high-grade tumours showing complex genomic aberrations. We have integrated genome-wide genetic and epigenetic profiles from the EuroBoNeT panel of 19 human osteosarcoma cell lines based...
ORGANISM(S): Homo sapiens 
2012-12-06 | E-GEOD-36002 | biostudies-arrayexpress
UnknownMethods that remove batch effects while retaining group differences may lead to exaggerated confidence in downstream analyses.
Not available
S-EPMC4679072 | biostudies-literature
UnknownA multiomic framework for predicting laryngo-esophageal dysfunction following induction chemotherapy in hypopharyngeal-laryngeal carcinoma.
Not available
S-EPMC12804047 | biostudies-literature
UnknownGenome build information is an essential part of genomic track files.
Not available
S-EPMC5599886 | biostudies-literature
UnknownTelomerase as a Target for Therapeutic Cancer Vaccines and Considerations for Optimizing Their Clinical Potential.
Not available
S-EPMC8288190 | biostudies-literature
UnknownAutomated amplicon design suitable for analysis of DNA variants by melting techniques.
Not available
S-EPMC4642734 | biostudies-literature
UnknownCooperative induction of receptor tyrosine kinases contributes to adaptive MAPK drug resistance in melanoma through the PI3K pathway.
Not available
S-EPMC9940011 | biostudies-literature
TranscriptomicsIntegrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma.
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
ORGANISM(S): Homo sapiens 
2012-12-06 | E-GEOD-36004 | biostudies-arrayexpress
UnknownClusTrack: feature extraction and similarity measures for clustering of genome-wide data sets.
Not available
S-EPMC4400084 | biostudies-literature
UnknownCauses for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift.
Not available
S-EPMC6406718 | biostudies-literature
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