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E-MTAB-9381 RNA-seq of coding RNA, Human - High-thr… Homo sapiens, Homo sapiens

RNA sequencing comparing the transcriptome of a severe congenital neutropenia (SCN) patient who progressed to AML (SCN-AML) with the SCN phase and healthy controls

·Released Aug. 24, 2020
5
Samples
5
Assays
1
References
Description

CD34+ hematopoietic stem progenitor cells (HSPCs) from cryo-preserved blood or bone marrow were FACS sorted in TriZol and RNA was isolated according to the manufacturer’s protocol. SMARTer Ultra Low Input RNA kit for sequencing (Clontech, v4 Cat# 634891) was used to generate cDNA. Sequencing libraries were generated using TruSeq Nano DNA Sample Preparation kits (Illumina, Cat# 20015964), according to the low sample protocol and paired-end sequenced on a HiSeq 2500 or Novaseq 6000 (both Illumina).

References
Malignant transformation involving CXXC4 mutations identified in a leukemic progression model of severe congenital neutropenia
Patricia A. Olofsen, Szabolcs Fatrai, Paulina M.H. van Strien, Julia C. Obenauer, Hans W.J. de Looper, Remco M. Hoogenboezem, Claudia A.J. Erpelinck-Verschueren, Michael P.W.M. Vermeulen, Onno Roovers, Torsten Haferlach, Joop H. Jansen, Mehrnaz Ghazvini, Eric M.J. Bindels, Rebekka K. Schneider, Emma M. de Pater, Ivo P. Touw
Sample Attributes
Organism
Homo sapiens
Cell type
hematopoietic stem cell
Phenotype
CD34 positive
Age
18 year, 26 year, 27 year, 12 year
Sex
male, female
Genotype
wild type genotype, ELANE-G203R
Developmental stage
adult, juvenile stage
Organism part
bone marrow, blood
Clinical history
none, Severe congenital neutropenia
Disease
normal, acute myeloid leukemia, Severe congenital neutropenia
Experiment Info
Accession
E-MTAB-9381
Type
RNA-seq of coding RNA, Human - High-throughput sequencing
Organism
Homo sapiens, Homo sapiens
Released
Aug. 24, 2020
Submitter
Patricia Olofsen、 Ivo Touw
External Links
ArrayExpress source
Analysis Services
Analysis Services

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