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SRX21625338: panel sequencing data
1 ILLUMINA (NextSeq 500) run: 8.3M spots, 2.5G bases, 752Mb downloads

Design: Genomic DNA was isolated from 2 to 5ml of subjects' peripheral blood sample using a commercial kit (TIANGEN, China). The targeted gene capture process was completed in MyGenostics, Beijing, China. Targeted next-generation sequencing with a panel of 208 genes related to blood system diseases was adopted to detect the variants. The library was sequenced using a NextSeq500 instrument.
Submitted by: Fudan university
Study: SPTB family
show Abstracthide Abstract
Integrative Preimplantation Genetic Testing Analysis for a Chinese Family with Hereditary Spherocytosis Caused by a Novel Splicing Variant of SPTB
Sample:
SAMN37277513 • SRS18796996 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: 123
Instrument: NextSeq 500
Strategy: AMPLICON
Source: GENOMIC
Selection: PCR
Layout: PAIRED
Runs: 1 run, 8.3M spots, 2.5G bases, 752Mb
Run# of Spots# of BasesSizePublished
SRR259052458,343,9862.5G752Mb2023-09-05

ID:
29259757

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