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SRX21640652: Whole exome sequencing of human sample 28
1 ILLUMINA (HiSeq X Ten) run: 36.7M spots, 11.1G bases, 4.2Gb downloads

Design: DAN was extracted and it was subjected for whole exome sequencing
Submitted by: Aravind medical research foundation
Study: To EXPLORING MITONUCLEAR GENETIC FACTORS IN LEBER'S HEREDITARY OPTIC NEUROPATHY: INSIGHTS FROM COMPREHENSIVE PROFILING OF UNIQUE CASES
show Abstracthide Abstract
This study investigate the genetic basis of thirty distinct LHON cases through comprehensive sequencing to identify mito-nuclear genetic factors involved in the disease pathogenesis. Our findings highlight the significance of nuclear gene involvement in cases of LHON exhibiting secondary mutations or inconclusive mtDNA mutations
Sample:
SAMN37294641 • SRS18810494 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: 356978_sample7
Instrument: HiSeq X Ten
Strategy: WXS
Source: GENOMIC
Selection: PCR
Layout: PAIRED
Runs: 1 run, 36.7M spots, 11.1G bases, 4.2Gb
Run# of Spots# of BasesSizePublished
SRR2592094136,747,16111.1G4.2Gb2023-09-06

ID:
29291259

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