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GenomicsGenomic landscape of IG-MYC positive Burkitt lymphoma with precursor B-cell immunophenotype.
As part of the ICGC, the ICGC MMML-Seq project performed whole genome sequencing of a rare Burkitt lymphoma subtype with precursor B-cell immunophenotype. Analysis were performed in concordance with the guidelines of the ICGC.
EGAS00001002968 | EGA
UnknownTranscriptional and Mutational Profiling of B-Other Acute Lymphoblastic Leukemia for Improved Diagnostics.
Not available
S-EPMC8616234 | biostudies-literature
UnknownIG-MYC + neoplasms with precursor B-cell phenotype are molecularly distinct from Burkitt lymphomas.
Not available
S-EPMC6251006 | biostudies-literature
UnknownLentiviral vector induced insertional haploinsufficiency of Ebf1 causes murine leukemia.
Not available
S-EPMC3369288 | biostudies-literature
Genomics233fa72b-87ef-4a9b-b96d-dfb6ca9543bd - samples
This dataset contains the aligned whole genome sequencing data of cell line 380. This cell was established from the peripheral blood of a 15-year-old boy with acute lymphoblastic leukemia at relapse, showing an immature phenotype and carrying an IGH-MYC (t(8;14)) as well as an IGH-BCL2 (t(14;18)) ch...
EGAD00001004090 | EGA
UnknownSubclonal analysis in a lobular breast cancer with classical and solid growth pattern mimicking a solid-papillary carcinoma.
Not available
S-EPMC5527319 | biostudies-literature
UnknownPsychological Distress and Coping Ability of Women at High Risk of Hereditary Breast and Ovarian Cancer before Undergoing Genetic Counseling-An Exploratory Study from Germany.
Not available
S-EPMC8073852 | biostudies-literature
UnknownFrequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP-BFM acute lymphoblastic leukemia protocol.
Not available
S-EPMC7540392 | biostudies-literature
UnknownBreast cancer susceptibility: current knowledge and implications for genetic counselling.
Not available
S-EPMC2947107 | biostudies-literature
UnknownBeyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies.
Not available
S-EPMC9320507 | biostudies-literature
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