官方服务:
资源简介:
KMT2A rearrangement detection in MLL patients
应用场景:
创建时间:
2023-07-12
相关数据集
Data_Sheet_1_Ultra-Sensitive CSF3R Deep Sequencing in Patients With Severe Congenital Neutropenia.doc
High frequency of acquired CSF3R (colony stimulating factor 3 receptor, granulocyte) mutations has been described in patients with severe congenital neutropenia (CN) at pre-leukemia stage and overt ac
NIAID Data Ecosystem40
3'-TARGET-seq: a novel method for high-sensitivity single-cell mutational analysis and parallel high throughput RNA-sequencing [Figures 5 and 6, Figure S7]. 3'-TARGET-seq: a novel method for high-sensitivity single-cell mutational analysis and parallel high throughput RNA-sequencing [Figures 5 and 6, Figure S7]
We developed 3'-TARGET-seq, a single-cell genotyping and RNA-seq method, which allows accurate detection of multiple mutations within single-cells from genomic and coding DNA in parallel with high thr
NIAID Data Ecosystem10
Genotyping of human 459 diagnostic AML samples
Genotyping of human 459 diagnostic AML samples
ChEBI2008-06-21 更新00
Percentage of positive cells for each LNA probe in 10 AMLs.
A simplified karyotype is reported in italics. NK = normal karyotype.
NIAID Data Ecosystem20
Success rate of clonality assays overall and in subgroups.
Success rate of clonality assays overall and in subgroups.
Figshare2019-03-22 更新10



