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Breast Cancer - Subtype defined by an amplification of the HER2 gene
Study
EGAS00001001431
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Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency
Study
EGAS00001000149
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A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Study
EGAS00001001539
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Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552
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PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
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The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer
Study
EGAS00001001573
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In_Situ_Transcription_whole_genome_sequencing
Study
EGAS00001001971
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FRCC_Exome_sequencing
Study
EGAS00001000176
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Signatures of mismatch repair deficiency in cancer genomes
Study
EGAS00001000182
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CML_blast_phase_rearrangement_screen
Study
EGAS00001000191