Accession	SAMC2059619
Accession in Other Database	GSA-Human: HRS344547
Sample name	HCM_LV_indH100
Title	human hearts: left ventricle (LV)
Sample type	Human sample
Organism	Homo sapiens
Description	To explore the mechanism of hypertrophic cardiomyopathy
Attributes	*This sample record contains additional controlled-access information that is avaiable from GSA-Human by requesting study HRA002044 in the GSA-Human system.
Release date	2024-02-28
BioProject Accession	PRJCA007579
Submitter	Mengya Liu (tangfuchou@pku.edu.cn)
Organization	Peking University
Submission date	2023-06-18

Sample Data

Resource name	Description
GSA-Human (1)	-
HRA002044 (Controlled Access)	Hypertrophic cardiomyopathy (HCM) is an inherited disorder that can leads to atrial fibrillation, heart failure and arrhythmic sudden death. It is characterized by unexplained left-ventricular hypertrophy. In this study, we collected 12 adult human left ventricles from HCM patients and used 8 adult human left ventricles from healthy donors who contributed for other reasons instead of cardiovascular disease and 3 fetal human left ventricles from aborted fetuses. To explore the mechanism of hypertrophic cardiomyopathy, we performed bulk RNA-seq and NOMe-seq for the left ventricle samples.

Resource name

Description

GSA-Human (1)

HRA002044 (Controlled Access)

Hypertrophic cardiomyopathy (HCM) is an inherited disorder that can leads to atrial fibrillation, heart failure and arrhythmic sudden death. It is characterized by unexplained left-ventricular hypertrophy. In this study, we collected 12 adult human left ventricles from HCM patients and used 8 adult human left ventricles from healthy donors who contributed for other reasons instead of cardiovascular disease and 3 fetal human left ventricles from aborted fetuses. To explore the mechanism of hypertrophic cardiomyopathy, we performed bulk RNA-seq and NOMe-seq for the left ventricle samples.

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