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Whole genome SNP array data from myelodysplastic syndromes (MDS) patients

ChEBI2014-05-22 更新2026-07-21 收录

血液肿瘤基因组学

SNP阵列遗传变异分析

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-57229 数据链接链接失效反馈

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资源简介：

Whole genome SNP array data from myelodysplastic syndromes (MDS) patients

应用场景：

创建时间：

2014-05-22

树突状肉瘤基因组分析

血液肿瘤基因组学

This is a comprehensive genomic analysis of a rare set of secondary histiocytic/dendritic sarcomas from the consult service of the Hematopathology section of the Laboratory of Pathology, NCI, NIH.

NIAID Data Ecosystem50

Sézary Syndrome Originates from Heavily Mutated Hematopoietic Progenitors

血液肿瘤基因组学

皮肤T细胞淋巴瘤

The pathogenesis of cutaneous T cell lymphoma (CTCL) remains unclear. To study the malignant transformation of CTCL, we collected matched hematopoietic stem cell (HSC) extracts from bone marrow, CD4+C

NIAID Data Ecosystem40

DNA-Seq of human Acute Panmyelosis with Myelofibrosis (APMF) Samples

血液肿瘤基因组学

DNA测序变异检测

DNA-Seq of human Acute Panmyelosis with Myelofibrosis (APMF) Samples

ChEBI2020-04-11 更新40

SNPs Array Karyotyping Reveals a Novel Recurrent 20p13 Amplification in Primary Myelofibrosis

血液肿瘤基因组学

纤维化分子病理

The molecular pathogenesis of primary mielofibrosis (PMF) is still largely unknown. Recently, single-nucleotide polymorphism arrays (SNP-A) allowed for genome-wide profiling of copy-number alterations

NIAID Data Ecosystem50

Recurrent CNAs reported by previous studies of MDS/AML and this study.

血液肿瘤基因组学

拷贝数变异分析

Recurrent CNAs reported by previous studies of MDS/AML and this study.

Figshare2016-10-31 更新40