官方服务:
资源简介:
WES data of an Iranian patient with LVWM
应用场景:
创建时间:
2021-06-28
相关数据集
HipSci Whole Exome sequencing HSP
The HipSci project brings together diverse constituents in genomics, proteomics, cell biology and clinical genetics to create a UK national iPS cell resource and use it to carry out cellular genetic s
NIAID Data Ecosystem70
Additional file 7 of Genome-wide association analysis unveils candidate genes and loci associated with aplasia cutis congenita in pigs
Additional file 7: Table S4. Pathway Enrichment Analysis Reveals Significantly Enriched KEGG and GO Pathways Related to ACC. Description: This file provides the enrichment of protein-coding genes in K
Figshare2024-08-16 更新40
Affymetrix CytoScan 750K array data for a parthenogenetic SMA human embryonic stem cell line
Affymetrix CytoScan 750K array data for a parthenogenetic SMA human embryonic stem cell line
ChEBI2015-09-01 更新30
Canis lupus familiaris breed:greyhound Raw sequence reads. Canis lupus familiaris breed:greyhound
Startle disease, or hyperekplexia, is a glycinergic disorder characterized by hypertonia and apnea that is triggered by noise and/or touch. The SLC6A5 gene encodes the presynaptic glycine transporter,
NIAID Data Ecosystem50
Application of array-CGH for the detection of genomic rearrangements responsible for syndromic mental retardation of unknown cause
Here we describe an interstitial pure duplication of 19p13.3 that was initially considered as a de novo alteration, in a patient with intellectual disability studied by array-CGH. The finding of the s
NIAID Data Ecosystem30



